136,99 €
A guide to the extraction, isolation and purification of bioactive compounds from agricultural wastes, and their applications Recovering Bioactive Compounds from Agricultural Wastes offers a guide to the many uses of agricultural wastes from the production of major food types including tea, coffee, cacao, cashew, fruit and vegetables, wine, edible oils, sugar, starch and more. Written by a noted expert in the field, the text explores the various methods for extraction, isolation and purification of bioactive compounds from agricultural wastes. The author also makes recommendations concerning the most effective applications of bioactive compounds and discusses the economics and market for recovered bioactive compounds. Recent studies reveal that bioactive compounds have been directly linked to biological activity such as antioxidant, anticancer, antidiabetic, anti-cardiovascular capacities, etc. In particular, agricultural wastes are considered as potential and inexpensive sources of bioactive compounds. Recovering Bioactive Compounds from Agricultural Wastes fills a gap in the literature by providing a text that explores this important topic and examines the: * Sustainability of waste management and shows how to extract, isolate and purify bioactive compounds from agricultural wastes, and their most effective application * Wide range of agricultural food produce that can be processed and the special techniques used for recovering the bioactive compounds from these sources * Health applications of bioactive compounds that have been directly linked to pharmacological activities including antioxidant, anticancer, and more Designed for use by researchers and producers in the agriculture, pharmaceuticals and nutraceuticals, Recovering Bioactive Compounds from Agricultural Wastes contains the knowledge, history and definition, classification and synthesis, and extraction techniques of bioactive compounds.
Sie lesen das E-Book in den Legimi-Apps auf:
Seitenzahl: 475
Veröffentlichungsjahr: 2017
Cover
Title Page
Copyright
Dedication
List of Contributors
About the Editor
Preface
Acknowledgements
Chapter 1: Potential, Uses and Future Perspectives of AgriculturalWastes
1.1 Introduction
1.2 Potential of Agricultural Wastes
1.3 Uses of Agricultural Wastes and Recovered Bioactive Compounds
1.4 Future Perspectives on the Use of Agricultural Wastes and Recovered Bioactive Compounds
1.5 Conclusion
References
Chapter 2: Bioactive Compounds and Extraction Techniques
2.1 History and Definition of Bioactive Compounds
2.2 Classification and Synthesis of Bioactive Compounds
2.3 Extraction of Bioactive Compounds
2.4 Conclusion
Acknowledgement
References
Chapter 3: Recovering Bioactive Compounds from Tea, Coffee, Cacao and Cashew Wastes
3.1 Introduction
3.2 Recovering Bioactive Compounds from Tea Wastes
3.3 Recovering Bioactive Compounds from Coffee Wastes
3.4 Recovering Bioactive Compounds from Cacao Wastes
3.5 Recovering Bioactive Compounds from Cashew Wastes
3.6 Conclusion
References
Chapter 4: Recovering Bioactive Compounds from Fruit and Vegetable Wastes
4.1 Introduction
4.2 Bioactive Compound Resources in Fruit and Vegetable Wastes
4.3 Recovering Bioactive Compounds from Fruit and Vegetable Wastes
4.4 Conclusion
References
Chapter 5: Recovering Bioactive Compounds from Wine Wastes
5.1 Introduction
5.2 Recovering Bioactive Compounds from Wine Wastes
5.3 Conclusion
References
Chapter 6: Recovering Bioactive Compounds from Edible Oil Wastes
6.1 Introduction
6.2 Edible Oil Processing and Byproducts
6.3 Recovering Bioactive Compounds from Edible Oil Wastes
6.4 Conclusion
References
Chapter 7: Recovering Bioactive Compounds from Cane Sugar Wastes
7.1 Introduction
7.2 Chemical Composition and Functional Properties of Sugarcane
7.3 Cane Sugar Production and Its Byproducts/Wastes
7.4 Recovering Bioactive Compounds from Cane Sugar Byproducts/Wastes
7.5 Conclusion
References
Chapter 8: Recovering Bioactive Compounds from Starch Wastes
8.1 Introduction
8.2 Recovery of Bioactive Compounds from Potato Wastes
8.3 Recovery of Bioactive Compounds from Rice and Wheat Wastes
8.4 Recovery of Bioactive Compounds from Other Starch Wastes
8.5 Conclusion
References
Chapter 9: Recovering Bioactive Compounds from Other Agricultural Wastes
9.1 Introduction
9.2 Recovering Bioactive Compounds from Pepper Waste
9.3 Recovering Bioactive Compounds from Onion Waste
9.5 Conclusion
Acknowledgements
References
Chapter 10: Economics and Market for Recovered Bioactive Compounds from Agricultural Wastes
10.1 Introduction
10.2 Economic Analysis of Recovered Bioactive Compounds
10.3 Market Analysis of Recovered Bioactive Compounds
10.4 Conclusion
References
Index
End User License Agreement
xi
xii
xiii
xiv
xv
xvii
1
2
6
10
11
12
13
14
15
16
17
18
19
20
21
22
23
24
26
27
28
29
30
31
32
33
34
35
36
37
38
39
40
41
42
43
44
45
46
47
48
49
50
51
52
53
55
56
57
58
59
60
61
62
63
64
65
66
67
68
69
70
71
72
73
74
75
76
77
78
79
81
82
83
84
85
88
89
90
91
92
93
94
95
96
97
98
99
101
102
103
104
105
106
107
108
109
110
111
112
113
114
115
116
117
118
120
121
122
123
124
125
126
127
128
129
130
131
132
133
134
135
136
137
138
139
140
141
142
143
144
145
146
147
148
149
150
151
152
153
154
155
156
157
158
159
160
161
162
163
164
165
166
167
168
169
170
173
174
175
176
177
178
179
180
181
182
183
184
185
186
187
188
189
190
191
192
193
194
197
198
199
200
201
202
203
204
205
206
207
208
209
210
211
212
213
214
215
216
217
218
219
221
222
223
224
225
226
227
228
229
230
231
232
233
234
236
237
238
239
240
241
242
243
244
245
246
247
248
249
251
252
253
254
255
256
257
258
259
260
261
262
Cover
Table of Contents
Preface
Begin Reading
Chapter 1: Potential, Uses and Future Perspectives of AgriculturalWastes
Figure 1.1 Major agricultural sectors in the recovery of bioactive compounds.
Figure 1.2 Chemical structures of (a) hydroxybenzoic and (b) hydroxycinnamic acids.
Figure 1.3 Chemical structures of major classes of flavonoids.
Figure 1.4 Chemical structures of some phenolic compounds from OMW.
Figure 1.5 Recovery of phenolic compounds from OMW
Figure 1.6 Recovery and concentration of phenolic components from wine byproducts.
Figure 1.7 Chemical structure of lignin secoisolariciresinol from flaxseed and its conversion products.
Figure 1.8 Chemical structures of phytochemicals withanti-aging potential.
Chapter 2: Bioactive Compounds and Extraction Techniques
Figure 2.1 Common pathways for secondary metabolite formation from primary metabolism.
Source:
Dewick (2001). Reproduced with permission of John Wiley & Sons.
Figure 2.2 Supercritical CO
2
extraction system.
Source:
Garmus et al. (2014). Reproduced with permission of Elsevier.
Figure 2.3 Pressurised liquid extraction (PLE) system.
Source:
Richter et al. (1996). Reproduced with permission of American Chemical Society.
Chapter 3: Recovering Bioactive Compounds from Tea, Coffee, Cacao and Cashew Wastes
Figure 3.1 Main steps in green and black tea production.
Figure 3.2 Chemical structure of (a) sesamin and (b) compound B isolated from methanol extract of tea seed oil.
Source:
Lee & Yen (2006). Reproduced with permission of American Chemical Society.
Figure 3.3 Experimental battery plant for solid–liquid extraction (SLE) of caffeine from tea waste with three extractors.
Source:
Senol & Aydin (2006). Reproduced with permission of Elsevier.
Figure 3.4 Flow diagram of the supercritical extraction set-up.
Source:
İçen & Gürü (2010). Reproduced with permission of Elsevier.
Figure 3.5 Schematic diagram of subcritical water extraction system. B, burette; CV, check valve; DN, drain; EC, extraction cell; F, fan; HX, heat exchanger; MF, microfilter; NV, needle valve; OV, oven; P, pump; PI, pressure indicator; PR, pressure regulator; RV, relief valve; TI, temperature indicator; TIC, temperature indicator controller; WI, water inlet; WO, water outlet.
Source:
Shalmashi et al. (2010). Reproduced with permission of John Wiley & Sons.
Figure 3.6 Chemical structures of caffeine, theophylline, gallic acid and four major catechins in tea products and wastes. GA, gallic acid; EGCG, (−)-epigallocatechin-3-gallate; EGC, (−)-epigallocatechin; ECG, (−)-epicatechin-3-gallate; EC, (−)-epicatechin.
Source:
Cabrera et al. (2006). Reproduced with permission of Taylor & Francis.
Figure 3.7 (a) Black tea stalk and (b) fibre obtained from black tea production.
Figure 3.8 Main steps in green coffee production.
Figure 3.9 Chemical structures of caffeine, trigonelline, chlorogenic acid and diterpene cafestol in coffee products and wastes.
Source:
Adapted from Nuhu (2014).
Figure 3.10 Spent coffee grounds discarded from soluble coffee production.
Figure 3.11 Main steps in soluble coffee production.
Figure 3.12 Flow diagram of a simplified supercritical fluid extraction (SFE) process.
Source:
Pereira & Meireles (2010). Reproduced with permission of Springer.
Figure 3.13 Main steps in cacao bean production.
Figure 3.14 Main steps in chocolate production
Figure 3.15 Main steps in cashew nut production.
Figure 3.16 Structures of the flavonoids in cashew apple.
Source:
de Brito et al. (2007). Reproduced with permission of Elsevier.
Figure 3.17 Chemical structures of the major phenolic constituents of cashew nut shell liquid (CNSL).
Source:
Paramashivappa et al. (2001). Reproduced with permission of American Chemical Society.
Figure 3.18 Flow chart for the separation of anacardic acid, cardol and cardanol from CNSL.
Source:
Paramashivappa et al. (2001). Reproduced with permission of American Chemical Society.
Figure 3.19 Supercritical fluid extraction (SFE) apparatus.
Source:
Smith et al. (2003). Reproduced with permission of Elsevier.
Figure 3.20 Flowchart of the SFE process.
Source:
Patel et al. (2006a). Reproduced with permission of Elsevier.
Chapter 4: Recovering Bioactive Compounds from Fruit and Vegetable Wastes
Figure 4.1 General process for the recovery of bioactive compounds from fruit and vegetable wastes. SE, solvent extraction; UAE, ultrasound-assisted extraction; MAE, microwave-assisted extraction; PLE, pressurised liquid extraction; SFE, supercritical fluid extraction; EAE, enzyme-assisted extraction.
Figure 4.2 Formation, growth and collapse of a cavitation bubble.
Source:
González-García et al. (2010), http://www.mdpi.com/2073-4441/2/1/28/htm. Used under CC BY 3.0 https://creativecommons.org/licenses/by/3.0/.
Figure 4.3 Typical reactor configurations: (a) ultrasonic bath, (b) transducer dipped in batch configuration, (c) transducer immersed in a flow reactor.
Source:
González-García et al. (2010), http://www.mdpi.com/2073-4441/2/1/28/htm. Used under CC BY 3.0 https://creativecommons.org/licenses/by/3.0/.
Figure 4.4 Pressurised liquid extraction (PLE) unit. ET, ethanol tank; HP, high-pressure pump; V1, V2, V3, valves; M, manometer; TC, temperature controller; EH, electric heater; EB, extraction bed; CF, collection flask.
Source:
Cardenas-Toro et al. (2015). Reproduced with permission of Elsevier.
Figure 4.5 SC-CO
2
extraction unit. 1, CO
2
cylinder; 2, refrigeration bath; 3, high-pressure pump; 4, CO
2
supply tank; 5, extractor; 6, peristaltic pump; 7, extract collection flask; 8, Porapak-Q volatiles trap; 9, gas flow metre; 10, volume totaliser; 11, heating bath.
Source:
Garcia-Mendoza et al. (2015). Reproduced with permission of Elsevier.
Chapter 5: Recovering Bioactive Compounds from Wine Wastes
Figure 5.1 Flow chart of while and red wine production.
Figure 5.2 Flow chart of supercritical fluid extraction (SFE) of polyphenols from grape bagasse.
Source:
Farías-Campomanes et al. (2013). Reproduced with permission of Elsevier.
Figure 5.3 Accumulated concentration of phenolic compounds in extracts from grape bagasse.
Source:
Farías-Campomanes et al. (2013). Reproduced with permission of Elsevier.
Figure 5.4 Chemical structures of the common classes of phenolics identified in grape pomace.
Source:
Fontana et al. (2013). Reproduced with permission of American Chemical Society.
Figure 5.5 (a) Experimental set-up for conventional extraction of high added-value molecules from plant matrices used at laboratory scale. (b) Ultrasound-assisted extraction (UAE) principle and cavitational phenomenon. (c) Microwave-assisted extraction (MAE) equipment used at laboratory scale, showing the molecular rotation mechanism.
Source:
Barba et al. (2016). Reproduced with permission of Elsevier.
Chapter 6: Recovering Bioactive Compounds from Edible Oil Wastes
Figure 6.1 Full processing flow chart for a general edible oil process.
Figure 6.2 Oleuropein and its derivatives after enzymatic hydrolysis by β-glycosidase and esterase.
Figure 6.3 Schematic principle of phenolic extraction by enzyme.
Figure 6.4 Optimised extraction procedure for the recovery of phenolic compounds from olive oil mill waste.
Figure 6.5 Supercritical fluid extraction (SFE) equipment. Liquid CO
2
is contained and kept at low temperature by a cooler (1) using a glycolic solution and pumped to a pre-heater by an air-pressure pump (2). The solvent is transferred to the pre-heater with CO
2
in different lines by an air-driven piston pump (3). At high pressure, the solvent and CO
2
are mixed together before being heated in a heat exchanger (4). The heated mixture passes through the extractor vessel (5), then goes to the other basket, which has a back pressure valve. Finally, liquid CO
2
expands into a tank, where the extracted substances are collected. The temperature and pressure of the extractor vessel aremonitored and controlled.
Figure 6.6 Process for producing concentrated and refined actives from tissues and byproducts of olive oils using membrane technologies. MF/UF, microfiltration/ultrafiltration; NF, nanofiltration; RO, reverse osmosis.
Figure 6.7 Recovery of sterols from deodorised oil distillate (DOD).
Figure 6.8 Recovery of sterols from deodorised oil distillate (DOD).
Figure 6.9 Recovery of sterols from deodorised oil distillate (DOD).
Figure 6.10 Recovery of sterols from deodorised oil distillate (DOD).
Figure 6.11 Recovery of phytosterols: (a) low sterol content and low-pH materials; (b) high sterol content and high-pH materials.
Figure 6.12 Two-step
in situ
reaction and distillation process for the purification of tocopherols and phytosterols from soybean DOD tocopherol/sterol concentrate.
Figure 6.13 Schematic diagram of an SC-CO
2
reaction unit.
Figure 6.14 Process for isolating soluble dietary fibres and valuable polyphenols from olive mill wastewater (OMW).
Figure 6.15 Scheme of the partial purification of mannitol in the hydrolysates obtained after hydrothermal treatment of alperujo.
Figure 6.16 Modified process for obtaining mannitol and its derivatives from two-phase olive mill wastewater (2POMW).
Chapter 7: Recovering Bioactive Compounds from Cane Sugar Wastes
Figure 7.1 Simplified diagram of the main products and byproducts of the cane sugar processing industry.
Figure 7.2 Scheme of coumaric acid production by alkaline hydrolysis from sugarcane bagasse.
Chapter 8: Recovering Bioactive Compounds from Starch Wastes
Figure 8.1 Flow chart of the potato chip and flour production process.
Figure 8.2 Products of the alkaline hydrolysis of chlorogenic acid.
Figure 8.3 Product of the hydrolysis of α-chaconine and α-solanine.
Figure 8.4 Flow chart of the rice and rice flour production process.
Figure 8.5 Chemical structures of some major phenolic compounds found in rice hull extracts.
Figure 8.6 Flow chart of the wheat flour production process.
Figure 8.7 Total phenolic content (TPC) of bran from two waxy wheat genotypes: (a) Svevo set and (b) N11 set.
Figure 8.8 Total phenolic content (TPC) of bran from four triticale genotypes: (a) GDS7 set (b) Trim set (c) Rhino set and (d) Rigel set.
Figure 8.9 Chemical structures of naturally occurring forms of vitamin E: tocopherols and tocotrienols.
Figure 8.10 Flow chart of the barley flour production process.
Figure 8.11 Flow chart of the maize flour production process.
Figure 8.12 Flow chart of the cassava flour production process.
Chapter 9: Recovering Bioactive Compounds from Other Agricultural Wastes
Figure 9.1 Simplified flow sheet for obtaining extract from pepper waste through solid–liquid extraction (SLE). S/F, solvent to feed mass ratio.
Figure 9.2 Flow sheet of microwave-assisted extraction (MAE) in the recovery of bioactive compounds from discarded pepper fruits and a diagram of the equipment commonly used in MAE processes.
Figure 9.3 Flow sheet of ultrasound-assisted extraction (UAE) in the recovery of bioactive compounds from pepper waste and a diagram of the equipment commonly used in UAE processes.
Figure 9.4 Simplified scheme of an extraction bed with continuous flow of a supercritical solvent (or mixture).
Figure 9.5 Diagrams of a supercritical fluid extraction (SFE) + ultrasound (US) unit and of the internal configuration of the extraction bed used in kinetic experiments. V-1, V-2, V-3, V-4 and V-5, control valves; V-6, micrometer valve; SV, safety valve; C, compressor; F, compressed air filter; CF, CO
2
filter; B1, cooling bath; P, pump; B2, heating bath; I-1 and I-2, pressure indicators; I-3, temperature indicator; IC-1, IC-2 and IC-3, indicators and controllers of ultrasound power, temperature of the extraction column and temperature of the micrometer valve, respectively; U, ultrasound probe; R, flow totaliser; F, flow meter; EC, extraction column.
Figure 9.6 Parts of the onion bulb considered as solid wastes.
Figure 9.7 Simplified flow sheet for obtaining extract from onion waste through conventional extraction.
Figure 9.8 Simplified flow sheet for obtaining extract from onion peels through subcritical water extraction (SWE).
Figure 9.9 Schematic drawing of extraction and particle formation on-line (EPFO) equipment.
Figure 9.10 Chemical structures of (a) quercetin, (b) quercetin-49-glycoside and (c) quercetin-3,49-diglycoside.
Figure 9.11 Process for dealing with cottonseed using a two-phase system (TPS).
Chapter 10: Economics and Market for Recovered Bioactive Compounds from Agricultural Wastes
Figure 10.1 Estimation of cost of manufacture (COM) for grape seed oil obtained by supercritical fluid extraction (SFE) at different extraction times and extractor volumes, with grape seed cost at US$2.70/ton. Dotted lines are the selling prices of oil obtained by cold pressing in Brazilian (US$40) and international (US$80) markets.
Figure 10.2 (a) Estimated cost of manufacture (COM) for bagasse extracts with different capacities of extractor at 0.005 (▪), 0.05 (▴) and 0.5 (•) m
3
. (b) Contribution of each component in the COM for different extractor capacities and extraction times. FCI, fixed capital investment; CRM, cost of raw materials; COL, cost of labour; CUT, cost of utilities.
Figure 10.3 (a) Effect of extractor capacity on cost of manufacture (COM) for jabuticaba (
Myrciaria cauliflora
) skin extract using various methods. (b) Contribution of each component in the COM using combined ultrasound-assisted extraction (UAE) and agitated-bed extraction (ABE) at different extractor capacities. CUT, cost of utilities; CRM, cost of raw materials; FCI, fixed capital investment; COL, cost of operational labour.
Figure 10.4 Cost of manufacture (COM) for jabuticaba (
Myrciaria cauliflora
) skin crude extract, anthocyanins and phenolic compounds using pressurised liquid extraction (PLE) with an extractor capacity of 0.3 m
3
across 9 minutes.
Figure 10.5 Cost of manufacture (COM) of extracts from
Anacardium occidentale
L. leaves using supercritical fluid extraction (SFE) under different extraction conditions and with different extractor capacities.
Figure 10.6 Share of costs in the cost of manufacture (COM) of extracts from
Anacardium occidentale
L. leaves using supercritical fluid extraction (SFE) with different extractor capacities. FCI, fixed capital investment; CRM, cost of raw materials; COL, cost of operational labour; CUT, cost of utilities; CQC, cost of quality control.
Figure 10.7 Cost of manufacture (COM) of extracts from
Anacardium occidentale
L. leaves using supercritical fluid extraction (SFE) under different experiment conditions: (a) 35 °C/300 bar and (b) 45 °C/200 bar.
Figure 10.8 (a) Cost of manufacture (COM) of curcuminoid-rich extracts as a function of processing time for different extractor vessel capacities, with the raw material price at US$7.91/kg. (b) Influence of the cost of raw materials on the COM of curcuminoid-rich extracts at an extractor capacity of 0.05 m
3
.
Figure 10.9 Potential markets for recovered bioactive compounds from agricultural wastes.
Figure 10.10 Global new active substances (NAS) available since 1996.
Chapter 1: Potential, Uses and Future Perspectives of AgriculturalWastes
Table 1.1 Total harvested crop area, total production and total gross agricultural production value in 2013.
Source:
FAOSTAT (2015)
Table 1.2 Total harvested area, total production and total gross production value of major crops in 2013, as well as their main residues/wastes.
Source:
FAOSTAT (2015)
Table 1.3 High added-value products from crop-based residues.
Source:
Santana-Méridas et al. (2012). Reproduced with permission of Springer
Table 1.4 High added-value products from processing-based residues.
Source:
Santana-Méridas et al. (2012). Reproduced with permission of Springer
Table 1.5 Phenolic compounds from agricultural byproducts.
Source:
Balasundram (2006). Reproduced with permission of Elsevier
Table 1.6 Molecule of interest, substrate from food wastes, extraction method and yield.
Source:
Baiano (2014), http://www.mdpi.com/1420-3049/19/9/14821/htm. Used under CC BY 3.0 https://creativecommons.org/licenses/by/3.0/
Table 1.7 Extraction yields, total extracTable polyphenols (TEP) and composition of crude extracts from agro-industrial wastes.
Source:
Moure et al. (2001). Reproduced with permission of Elsevier
Table 1.8 Antioxidant activity of extracts from agro-industrial residues.
Source:
Moure et al. (2001). Reproduced with permission of Elsevier
Table 1.9 Plants with anti-aging capacity and their mechanisms of action.
Source:
Mukherjee et al. (2011). Reproduced with permission of Elsevier
Chapter 3: Recovering Bioactive Compounds from Tea, Coffee, Cacao and Cashew Wastes
Table 3.1 Mass proportion of cacao pod.
Source:
Nguyen (2014). Reproduced with permission of John Wiley & Sons
Chapter 4: Recovering Bioactive Compounds from Fruit and Vegetable Wastes
Table 4.1 Bioactive compound resources from fruit and vegeTable wastes
Table 4.2 Bioactive compounds recovered from fruit and vegeTable wastes using different extraction methods
Chapter 5: Recovering Bioactive Compounds from Wine Wastes
Table 5.1 Operational conditions and phenolic compounds in extracts from grape bagasse.
Source:
Farías-Campomanes et al. (2013). Reproduced with permission of Elsevier
Table 5.2 Content of phenolic compounds in the different residual parts of Albariño grape (mg/100 g of fresh weight).
Source:
Di Lecce et al. (2014). Reproduced with permission of Elsevier
Table 5.3 Phenolic compounds of extracts from chenin blanc, petit verdot and syrah pomace and rachis.
Source:
Melo et al. (2015). Reproduced with permission of Elsevier
Table 5.4 Antioxidant capacities of extracts from chenin blanc, petit verdot and syrah pomace and rachis.
Source:
Melo et al. (2015). Reproduced with permission of Elsevier
Table 5.5 Concentrations of total flavonoids (mg/g dried weight) and total polyphenols (mg GAE/g dried weight) extracted by two ternary solvent mixtures in different proportions.
Source:
Bosso et al. (2016). Reproduced with permission of Elsevier
Table 5.6 Total yield and phenolic, flavonoid and anthocyanin contents in extracts from four grape pomaces.
Source:
Xu et al. (2016). Reproduced with permission of John Wiley & Sons
Table 5.7 Tannins, condensed tannins and antioxidant activities in extracts from four grape pomaces.
Source:
Xu et al. (2016). Reproduced with permission of John Wiley & Sons
Table 5.8 Major individual flavonoids in extracts from four grape pomaces.
Source:
Xu et al. (2016). Reproduced with permission of John Wiley & Sons
Table 5.9 Solid–liquid extraction (SLE) techniques for phenolics from grape pomace.
Source:
Fontana et al. (2013). Reproduced with permission of American Chemical Society
Table 5.10 Application of nonconventional technologies to improve the extraction of valuable compounds from winery wastes and byproducts.
Source:
Barba et al. (2016). Reproduced with permission of Elsevier
Table 5.11 Comparison of extracTable amounts of resveratrol in grape skins and seeds (µg/g fresh weight) among different genotype groups and different intended usages.
Source:
Li et al. (2006). Reproduced with permission of American Chemical Society
Table 5.12 Dietary fibre content of five varieties of wine grape pomace skins. NS, neutral sugar; UA, uronic acid.
Source:
Deng et al. (2011). Reproduced with permission of Elsevier
Chapter 6: Recovering Bioactive Compounds from Edible Oil Wastes
Table 6.1 Annual production of major vegeTable oils (million tonnes) from 2010/11 to 2015/16 (forecast).
Source:
USDA figures (May 2015)
Chapter 8: Recovering Bioactive Compounds from Starch Wastes
Table 8.1 Phenolic compounds (mg/100 g fresh weight) extracted from potato peel using different organic solvents.
Source:
Singh & Saldaña (2011). Reproduced with permission of Elsevier
Table 8.2 Total phenolic content (TPC) (mg/100 g) from various potato peel varieties.
Source:
Singh & Saldaña (2011). Reproduced with permission of Elsevier
Table 8.3 Phenolic compounds (mg/100 g wet basic) extracted with subcritical water at different temperatures.
Source:
Singh & Saldaña (2011). Reproduced with permission of Elsevier
Table 8.4 Optimal conditions for extracting antioxidant compounds using three different extraction methods: DPPH radical scavenging activity (DPPH, mg TE/100 g dry weight), phenolic content (FCR, mg GAE/100 g dry weight) and caffeic acid content (CA, µg caffeic acid/g dry weight).
Source:
Wijngaard et al. (2012). Reproduced with permission of Elsevier
Table 8.5 Steroidal alkaloid contents under optimal ultrasound-assisted extraction (UAE) conditions in comparison to conventional solid–liquid extraction (SLE).
Source:
Hossain et al. (2014). Reproduced with permission of Elsevier
Table 8.6 Recovery of polyphenols from rice husk using different solvent extraction conditions.
Source:
Vadivel & Brindha (2015). Reproduced with permission of Elsevier
Table 8.7 Recovery of polyphenols from rice husk using acid and alkali hydrolysis.
Source:
Vadivel & Brindha (2015). Reproduced with permission of Elsevier
Table 8.8 Phenolic acid composition (µg/g sample) of waxy wheat bran.
Source:
Jonnala et al. (2010). Reproduced with permission of Elsevier
Table 8.9 Phenolic acid composition (µg/g sample) of triticales.
Source:
Jonnala et al. (2010). Reproduced with permission of Elsevier
Table 8.10 Chemical composition of oil extracted from durum wheat bran by supercritical carbon dioxide (SC-CO
2
) and Soxhlet.
Source:
Durante et al. (2012). Reproduced with permission of Springer
Table 8.11 Protein, lipid, ash (% wet basis), β-glucans (g/100 g wet basis) and tocols (mg/kg wet basis) in barley byproducts.
Source:
Panfili et al. (2008). Reproduced with permission of Elsevier
Table 8.12 Contents of individual tocols (mg/kg wet basis) and tocotrienol/tocopherol (T3/T) ratios in barley byproducts.
Source:
Panfili et al. (2008). Reproduced with permission of Elsevier
Chapter 9: Recovering Bioactive Compounds from Other Agricultural Wastes
Table 9.1 Microwave-assisted extraction (MAE) conditions applied in the recovery of compounds from pepper waste
Table 9.2 Ultrasound-assisted extraction (UAE) conditions applied in the recovery of compounds from pepper waste
Table 9.3 Composition (% of total peak area) of black pepper essential oil obtained by supercritical fluid extraction (SFE) and hydrodistillation.
Source:
Perakis et al. (2005). Reproduced with permission of Elsevier
Table 9.4 Bioactive compounds recovered from onion waste
Table 9.5 Tocopherol composition (mg/100 g cottonseed) and phytosterol composition (mg/100 g oil) after recovery of bioactive compounds from cotton waste.
Source:
Adapted from Mariod et al. (2011)
Chapter 10: Economics and Market for Recovered Bioactive Compounds from Agricultural Wastes
Table 10.1 Economic parameters used for the estimation of cost of manufacture (COM) of grape seed oil.
Source:
Prado et al. (2012). Reproduced with permission of Elsevier
Table 10.3 Economic evaluation of grape seed oil using supercritical fluid extraction (SFE) with raw material cost at US$2.70/ton.
Source:
Prado et al. (2012). Reproduced with permission of Elsevier
Table 10.4 Estimated cost of manufacture (COM) for jabuticaba (
Myrciaria cauliflora
) skin extract using UAE, ABE, combined UAE and ABE, Soxhlet with ethanol and Soxhlet with acidified ethanol_pH 3.
Source:
Santos et al. (2010). Reproduced with permission of Elsevier
Table 10.5 Cost of manufacture (COM) for jabuticaba (
Myrciaria cauliflora
) skin crude extract, phenolic compounds and anthocyanins using pressurised liquid extraction (PLE) with different extractor capacities over 9 minutes.
Source:
Santos et al. (2012). Reproduced with permission of Elsevier
Table 10.6 Contribution of each component to the cost of manufacture (COM) of jabuticaba (
Myrciaria cauliflora
) skin extracts using pressurised liquid extraction (PLE) with an extractor capacity of 0.3 m
3
.
Source:
Santos et al. (2012). Reproduced with permission of Elsevier
Table 10.7 Economic parameters used to estimate the cost of manufacture (COM) of extracts from pressed palm fibre (PPF).
Source:
Cardenas-Toro et al. (2015). Reproduced with permission of Elsevier
Table 10.8 Cost of manufacture (COM) for carotenoid-rich extract obtained from pressed palm fibre (PPF) by Soxhlet extraction (LPSE-SOX), percolation (LPSE-PE) and pressurised liquid extraction (PLE) with extraction units of 2 × 0.005 m
3
, 2 × 0.05 m
3
and 2 × 0.5 m
3
.
Source:
Cardenas-Toro et al. (2015). Reproduced with permission of Elsevier
Table 10.9 Economic parameters used to estimate the cost of manufacture (COM) of extracts from
Anacardium occidentale
L. leaves using supercritical fluid extraction (SFE).
Source:
Leitão et al. (2013). Reproduced with permission of Elsevier
Table 10.10 Economic parameters used to estimate the cost of manufacture (COM) of crude extracts from jussara pulp (
Euterpe edulis
) using ultrasound-assisted extraction (UAE) and agitated-bed extraction (ABE).
Source:
Vieira et al. (2013). Reproduced with permission of Elsevier
Table 10.11 Share of costs in the cost of manufacture (COM) of crude extracts from jussara pulp (
Euterpe edulis
) using ultrasound-assisted extraction (UAE) and agitated-bed extraction (ABE).
Source:
Vieira et al. (2013). Reproduced with permission of Elsevier
Table 10.12 Economic parameters used to estimate the cost of manufacture (COM) of curcuminoids from deflavoured turmeric (
Curcuma longa
L.) using pressurised liquids.
Source:
Osorio-Tobón et al. (2014). Reproduced with permission of Elsevier
Table 10.13 Economic parameters used to estimate the cost of manufacture (COM) of phenolic-rich extracts from Brazilian plants using supercritical and subcritical fluid extraction.
Source:
Veggi et al. (2014). Reproduced with permission of Elsevier
Table 10.14 Cost of manufacture of crude extracts (COM
EY
) and of the phenolic-rich fraction (COM
TPC
) using supercritical fluid extraction (SFE) with different solvent systems and with extractor capacities of 0.005, 0.05 and 0.5 m
3
.
Source:
Veggi et al. (2014). Reproduced with permission of Elsevier
Table 10.15 Shares in the cost of manufacture (COM) of Brazilian plant extracts using supercritical fluid extraction (SFE) with different solvent systems and with extractor capacities of 0.005, 0.05 and 0.5 m
3
.
Source:
Veggi et al. (2014). Reproduced with permission of Elsevier
Table 10.16 Estimated global market size for functional foods.
Source:
Adapted from Malla et al. (2013)
Table 10.17 Region and leading country spending on pharmaceuticals.
Source:
Adapted from Aitken & Kleinrock (2015)
Edited by Van Tang Nguyen
University of Newcastle, Australia Nha Trang University, Vietnam
This edition first published 2017
© 2017 John Wiley & Sons, Ltd
All rights reserved. No part of this publication may be reproduced, stored in a retrieval system, or transmitted, in any form or by any means, electronic, mechanical, photocopying, recording or otherwise, except as permitted by law. Advice on how to obtain permission to reuse material from this title is available at http://www.wiley.com/go/permissions.
The right of Van Tang Nguyen to be identified as the author of the editorial material in this work has been asserted in accordance with law.
Registered Offices
John Wiley & Sons, Inc., 111 River Street, Hoboken, NJ 07030, USA
John Wiley & Sons Ltd, The Atrium, Southern Gate, Chichester, West Sussex, PO19 8SQ, UK
Editorial Office
The Atrium, Southern Gate, Chichester, West Sussex, PO19 8SQ, UK
For details of our global editorial offices, customer services, and more information about Wiley products visit us at www.wiley.com.
Wiley also publishes its books in a variety of electronic formats and by print-on-demand. Some content that appears in standard print versions of this book may not be available in other formats.
Limit of Liability/Disclaimer of Warranty
The publisher and the authors make no representations or warranties with respect to the accuracy or completeness of the contents of this work and specifically disclaim all warranties, including without limitation any implied warranties of fitness for a particular purpose. This work is sold with the understanding that the publisher is not engaged in rendering professional services. The advice and strategies contained herein may not be suitable for every situation. In view of ongoing research, equipment modifications, changes in governmental regulations, and the constant flow of information relating to the use of experimental reagents, equipment, and devices, the reader is urged to review and evaluate the information provided in the package insert or instructions for each chemical, piece of equipment, reagent, or device for, among other things, any changes in the instructions or indication of usage and for added warnings and precautions. The fact that an organization or website is referred to in this work as a citation and/or potential source of further information does not mean that the author or the publisher endorses the information the organization or website may provide or recommendations it may make. Further, readers should be aware that websites listed in this work may have changed or disappeared between when this works was written and when it is read. No warranty may be created or extended by any promotional statements for this work. Neither the publisher nor the author shall be liable for any damages arising here from.
Library of Congress Cataloging-in-Publication Data
Names: Nguyen, Van Tang, 1979- editor.
Title: Recovering bioactive compounds from agricultural wastes / edited by Van Tang Nguyen.
Description: Hoboken, NJ : John Wiley & Sons, 2017. | Includes bibliographical references and index. |
Identifiers: LCCN 2017009461 (print) | LCCN 2017018525 (ebook) | ISBN 9781119168836 (ePDF) | ISBN 9781119168843 (ePub) | ISBN 9781119168829 (cloth)
Subjects: LCSH: Bioactive compounds. | Agricultural wastes-Recycling.
Classification: LCC QP517.B44 (ebook) | LCC QP517.B44 R43 2017 (print) | DDC 363.72/88-dc23
LC record available at https://lccn.loc.gov/2017009461
Cover Design: Wiley
Cover Images: Courtesy of Van Tang Nguyen
This book is dedicated to my dad Van Tac Nguyen, my mom Thi Thuy Duong, my wife Thi Le Nguyen, my son Trong Nhan Nguyen and my daughter Dan Thanh Nguyen.
Md. Ariful Alam
Department of Pharmaceutical Technology, Faculty of Pharmacy, International Islamic University Malaysia (IIUM), Pahang, Malaysia
Fiorella P. Cárdenas-Toro
Department of Engineering,Section of Industrial Engineering,Pontifical Catholic University of Peru,San Miguel, Lima, Peru
Sahena Ferdosh
Department of Plant Science,Faculty of Science,International Islamic University Malaysia (IIUM),Kuantan Campus,Pahang, Malaysia
Kashif Ghafoor
Department of Food Science and Nutrition,King Saud University,Riyadh, Saudi Arabia
Rukshana Akter Happy
Department of Biochemistry and Biotechnology,Faculty of Basic Medical and Pharmaceutical Sciences,University of Science and Technology Chittagong (USTC),Foy's Lake, Chittagong, Bangladesh
Thang Trung Khong
Nha Trang University, Nha Trang, Khanh Hoa, Vietnam
Van Tang Nguyen
School of Environmental and Life Sciences,Faculty of Science and Information Technology,University of Newcastle, Ourimbah, NSW, Australia
and
Department of Food Technology,Faculty of Food Technology,Nha Trang University,Nha Trang, Khanh Hoa, Vietnam
Hong Ngoc Thuy Pham
School of Environmental and Life Sciences,Faculty of Science and Information Technology,University of Newcastle,Ourimbah, NSW, Australia
and
Department of Postharvest Technology,Faculty of Food Technology,Nha Trang University,Nha Trang, Khanh Hoa, Vietnam
Md. Zaidul Islam Sarker
Department of Pharmaceutical Technology,Faculty of Pharmacy,International Islamic University Malaysia (IIUM),Pahang, Malaysia
Nguyen Thi Thao
Department of Quality Management,School of Biotechnology and Food Technology,Hanoi University of Science and Technology,Hanoi, Vietnam
Hoang Quoc Tuan
Department of Quality Management,School of Biotechnology and Food Technology,Hanoi University of Science and Technology,Hanoi, Vietnam
Giovani L. Zabot
Federal University of Santa Maria (UFSM),Cachoeira do Sul, RS, Brazil
Van Tang Nguyen was born in Hai Duong province, Vietnam. He obtained an Engineer degree in Food Technology from the Hanoi University of Science and Technology, Vietnam. He then received a Master's degree in Food Science from the National Taiwan Ocean University, Taiwan and a PhD in Food Science from the University of Newcastle, Australia. He has worked as a Demonstrator in Food Science and Human Nutrition at the School of Environmental and Life Sciences, Faculty of Science and Information Technology, University of Newcastle, Australia. He also works as a Lecturer in Food Technology at the Department of Food Technology, Faculty of Food Technology, Nha Trang University, Vietnam. His research has focused on natural bioactive compounds, pharmacological activity, value-added products and functional foods. His current expertise is in the extraction, isolation and quantification of bioactive compounds from natural materials and the determination of biological activity in vitro and in vivo.
Van Tang Nguyen has been interested in the use of agricultural residues/byproducts from the processing and production of food products for the production of value-added products for over a decade. He has published more than 25 research papers in peer-reviewed journals (Food Science, Chemical Papers, Drying Technology, Chemistry and Biodiversity, Industrial Crops and Products, Food Processing and Preservation, etc.) and has authored/edited five book chapters and five books in the field of Food Science and Technology. He has presented over 15 scientific reports at international conferences and served as the reviewer for many reputed journals (Food Science, Food Biochemistry, Pharmaceutical Biology, Industrial Crops and Products, Current Pharmaceutical Research, and so on). He is currently Editor-in-Chief and Founder of Bioactive Research and a member of the Institute of Food Technologist (USA) and Pancreatic Cancer Research Group (Australia).
Van Tang Nguyen is married to Thi Le Nguyen. They have two children, Trong Nhan Nguyen and Dan Thanh Nguyen.
Agriculture is regarded as one of the most important fields of human industry, due to its role in ensuring global food security for over 7 billion people around the world and supporting other industries. Agricultural production creates a great amount of residues/byproducts, which are considered ‘wastes’. Interestingly, agricultural wastes contain many valuable bioactive compounds, possessing a wide range of potential pharmacological properties, which have great contributions to make in related industries, such as nutraceuticals/functional foods, medicines, pharmaceuticals and cosmetics. However, they are still underutilised as abundant, inexpensive, renewable and sustainable sources of natural bioactive compounds.
In order to increase the value of agricultural production, reduce pollution risks and promote the development of related industries, we have prepared Recovering Bioactive Compounds from Agricultural Wastes to introduce the potential of agricultural wastes obtaining from the different sectors of agricultural production, such as tea, coffee, cacao, cashew, fruit and vegetable, wine, edible oil, starch and sugar, and to present, discuss and recommend various techniques for the extraction, isolation, purification and application of these bioactive compounds in different fields. We also discuss the economic and market analysis of agricultural wastes and bioactive compounds derived from these sources, based on a number of actual recovery processes to be established at pilot and industrial scales. Hopefully, this book will be a helpful reference for researchers, producers and traders in agricultural production and related industries.
Van Tang Nguyen, Editor University of Newcastle, Australia Nha Trang University, Vietnam
I would like to express my special thanks to John Wiley & Sons for their suggestions and effective cooperation in the preparation and completion of the manuscript of this book. I also sincerely acknowledge the reviewers for their comments on the proposal. I kindly thank all the authors for their valuable contribution to the chapters; their effort is highly appreciated and adequately recorded in this book. Last but not least, I would like to thank my colleagues, friends and family for their support, encouragement and special interest in the preparation and publication of this book.
Van Tang Nguyen
School of Environmental and Life Sciences, Faculty of Science and Information Technology, University of Newcastle, Ourimbah, NSW, Australia
Department of Food Technology, Faculty of Food Technology, Nha Trang University, Nha Trang, Khanh Hoa, Vietnam
Agriculture has a developmental history going back thousands of years and is considered one of the most important fields of human knowledge because of its special role in ensuring global food security for over 7 billion people around the world. It also has an important role in supporting and promoting the development of other industries, such as nutraceuticals, medicines, pharmaceuticals and cosmetics. In particular, agriculture produces a large amount of wastes, containing a significant quantity of valuable bioactive compounds, such as polyphenols, phenolic acids, flavonols, flavanols, flavonoids, procyanidins, proanthocyanidins, anthocyanins, glycosides, carotenoids, saponins, tannins, alkaloids, sterols, steroids, triterpenes, quinones, peptides and carbohydrates, which have been proved to possess a variety of biological activities, including antioxidant, antibacterial, antifungal, antiviral, antimicrobial, antidiabetic, anticancer, antidiarrhoeal, antihypertensive, antimutagenic, anti-inflammatory, anticholesterol and anticardiovascular properties (Figure 1.1) (Balasundram et al., 2006; Santana-Méridas et al., 2012). However, the utilisation of agricultural wastes as an abundant, biorenewable and low-cost source for the production of high value-added products is still under investigation, with limited outcomes. Therefore, research is needed into the application of environmentally friendly traditional and advanced techniques with low production costs in the extraction, isolation and purification of phytochemical compounds from agricultural wastes in high yields and at maximal quality. This strategy will increase the value of agricultural wastes and reduce pollution risks for the environment in both the short and the long term, and will enable sustainable development, one of the most important goals of modern global agricultural production.
Figure 1.1 Major agricultural sectors in the recovery of bioactive compounds.
According to the Food and Agriculture Organization of the United Nations (FAOSTAT, 2015), the total harvested crop area worldwide in 2013 was about 4.36 billion ha, producing approximately 21.70 billion tonnes, with a total gross production value of US$24 932.32 billion (Table 1.1). In Asia, the total harvested crops area was 1.82 billion ha (41.81% of total), producing 9.94 billion tonnes (45.80%), with a total gross production value of US$15 543.06 billion (62.34%).
Table 1.1 Total harvested crop area, total production and total gross agricultural production value in 2013. Source: FAOSTAT (2015)
Location
Total harvested area (billion ha)
Total production (billion tonnes)
Total gross production value (billion US$)
Africa
0.71
1.90
1295.47
Americas
0.89
5.22
3503.55
Asia
1.82
9.94
15543.06
Europe
0.86
4.43
4350.89
Oceania
0.08
0.21
239.35
Total
4.36
21.70
24932.32
Table 1.2 Total harvested area, total production and total gross production value of major crops in 2013, as well as their main residues/wastes. Source: FAOSTAT (2015)
Crop
Total harvested area (million ha)
Total production (million tonnes)
Total gross production value (billion US$)
Main residues/wastes
Tea, coffee, cacao and cashew
Tea
3.52
5.35
22.22
Fruit, flower, old leaves, dust, stalk and fibre
Coffee
10.14
8.92
16.37
Outer skin, pulp/mucilage, parchment/hull/husk, silver skin and spent coffee grounds
Cacao
10.01
4.59
6.95
Leaves, shell, husk, pulp/mucilage and hull
Cashew
5.46
4.44
2.82
cashew apple, outer shell, inner skin and nut shell
Fruits and vegetables
Fruit fresh nes
5.01
33.52
13.39
Peels, pulps, seeds, stalks and skins
Vegetable fresh nes
19.79
280
135.42
Leaves, stems, peels, skins and seeds
Wine production crops
Grapes
7.16
77.18
78.50
Pomace (seeds, skins), leaves, stalks, rachis and lees
Edible oil production crops
Palm fruit
18.05
266
31.34
Shells, husks and fronts
Olives
10.31
20.40
19.47
Leaves and stalks
Coconuts
12.07
62.45
10.47
Shells, husks and fronts
Soybeans
112
276
131.26
Straw and pods
Sunflower seed
25.45
44.55
26.08
Foliage and stems
Rapeseed
36.50
72.70
53.13
Straw
Cotton seed
n/r
47.07
9.75
Stalks
Sugar production crops
Beet
4.37
247
14.04
Roots, pulps and scums
Cane
26.94
1910
108.55
Leaves, tops and bagasse
Others
0.12
0.93
nr
Pulps and bagasse
Starch production crops
Rice
165
741
429.27
Straw, husk and bran
Wheat
219
716
242.25
Straw
Maize
185
1020
382.34
Straw, stalks and cobs
Potatoes
19.34
376
149.51
Foliage, tops, peels and pulps
Cassava
20.39
277
47.31
Peels, stalks and bagasse
Barley
49.15
144
36.30
Straw
Other crops
Beans, dry
29.05
22.81
16.06
Straw and pods
Beans, green
1.54
21.37
40.53
Straw and pods
Pepper
0.48
0.47
2.88
Leaves and stems
Seed cotton
32.17
73.05
82.62
Stalk
n/r, not reported
Table 1.3 High added-value products from crop-based residues. Source: Santana-Méridas et al. (2012). Reproduced with permission of Springer
Activity
Species
Waste type
Bioactive compounds
Applications
Horticultural production
Melon
Cucumis melo
Aerial biomass
Xanthan
Rheology modifier, food additive
Broccoli
Brassica oleracea
Aerial biomass
Glucosinolates, phenolic acids, flavonoids, vitamin C
Antioxidant
Carrot
Daucus carota
Roots
Hydroxycinnamic acid, anthocyanins
Antioxidant
Spinach
Spinacea oleracea
Leaves
Flavonoids
Antioxidant
Pepper
Capsicum annuum
Leaves, stems
Capsaicin, dihydrocapsaicin
Antioxidant, anti-inflammatory
Cucumber
Cucumis sativus
Leaves
Isovitexin, saponarin, vicenin-2, apigenin
Antioxidant
Tomato
Lycopersicum sculentum
Leaves
Solanesol
Antibacterial, anti-inflammatory
Cereal production
Wheat
Triticum
sp.
Straw
Xylose, polyphenols
Food ingredient
Others
sp.
Straw
Lignin
Value-added products
Tuber production
Potato
Solanum tuberosum
Leaves
Solanesol
Antibacterial, anti-inflammatory
Fruit production
Ginja cherry
Prunus cerasus
Stems, leaves
Polyphenols (catechin > 70%)
Antioxidant, antimicrobial
Pineapple
Ananus comosus
Straw (leaves)
Fibre
Polymer reinforcement
Grass production
Ryegrass
Lolium perenne
Grass chaff
β-adenosine
Mushroom production
Miscanthus
Miscanthus
× giganteus
Biomass
Lignin, phenols, sterols
Fuel, antioxidant, anticholesterol
Oil production
Olive
Olea europaea
Leaves
Polyphenols
Antimicrobial, antioxidant
Medicinal and condimentary herbs
Creosote bush
Larrea tridentate
Leaves
Poly and monomeric phenols
Antifungal
Saffron
Crocus sativus
Leaves
Kaempferol, orientin, vitexin
Antioxidant
Table 1.4 High added-value products from processing-based residues. Source: Santana-Méridas et al. (2012). Reproduced with permission of Springer
Activity/crops
Species
Waste type
Bioactive compounds
Activity/applications
Fresh fruit industry
Mango
Mangifera indica
Peels, pits/seeds
Tannins, vanillin, mangiferin
Antioxidant
Apple
Malus domestica
Pomace (peels, core, seeds, calyces, stems)
Pectin, catechins, hydroxycinnamates, phloretin glycosides, quercetin glycosides, procyanidins
Antioxidant
Watermelon
Citrullus lanatus
Rinds, flesh
Lycopene, citrulline, phenolic compounds
Antioxidant, food additives
Rambutan
Nephelium lappaceum
Peels
Ellagitannins
Antioxidant
Mangosteen
Garcinia mangostana
Pericarps
Proanthocyanidins
Antioxidant
Guajava
Psidium guajava
Bagasse
Epicatechin, quercetin, syringic acid, mirycetin
Antimicrobial
Banana
Musa sapientum
Dried leaves, pseudostems
Sugars
Fermentation
Peels
α-amilasa, laccasa, citric acid
Enzyme production
Lemon
Citrus limon
Peels
Flavanoids, saponins, tannins, alkaloids, steroids, triterpenes
Antimicrobial
Essential oil
Nematostatic activity
Limonene
Insecticidal (larvicidal)
Orange
Citrus sinensis
Peels
Citric acid
Additive, detergent, cosmetic
Essential oil
Nematostatic activity
Pineapple
Ananus comosus
Peels, core, crowns, stems
Bromelain
Food and textile industries, anti-inflammatory, anti-diarrhea, digestive
Pomegranate
Punica granatum
Husks
Poly- and monomeric phenols
Antifungal
Grapefruit
Citrus paradisi
Peels
Essential oil
Nematostatic activity
Mandarin
Citrus reticulata
Peels
Phenolic compounds
Antioxidant, antimicrobial
Papaya
Carica papaya
Peels, seeds
Phenolic compounds
Antioxidant, antimicrobial
Bergamot
Citrus bergamia
White tissues
Brutieridin, melitidin
Anticholesterolaemic
Seeds
Limonoids
Antiviral
Satsuma mandarin
Citrus unshiu
Peels
Hesperidin, narirutin, quercetagetin
Antioxidant
Citrus fruits
Citrus
sp.
Seeds, molasses
Limonoids
Anticancer
Peels
Flavonoids (hesperidin, diosmin, narirutin, didymin, sinesetin), carotenoids (violaxanthin, β-crytoxanthin, β-carotene), vitamin C, essential oils (limonene), minerals
Antioxidant
Horticultural industry
Artichoke
Cynara scolymus
Bracts, receptacles, stems, juice, heads
Neochlorogenic acid, chlorogenic acid, caffeoylquinic acids
Antioxidant
Beet
Beta vulgaris
Stalks
Azelaic acid
Antimicrobial
Onion
Allium cepa
Fresh peeling
Condensed tannins, flavonoids, quercetin aglycone
Antioxidant, textile dyes
Skins, top–bottom wastes, scales, discarded onions
Flavonoids, fructans and alk(en)yl cystein sulphoxides, quercetin aglycone, minerals
Antioxidant, dietary fibre
Tomato
Solanum lycopersicum
Seeds, pulps, skins
Lycopene, β-carotene, sterols, tocopherols, terpenes, glycoalkaloids
Antioxidant, anticholesterol
Coffee industry
Coffee
Coffea Arabica
Spent coffee grounds
Caffeine, chlorogenic acid
Allelopathy
Dry fruit industry
Peanut
Arachis hypogaea
Skins, seed coats
Polyphenols oligomeric proanthocyanidins, indole alkaloids, phenolic acids
Antioxidant anticancer, Blood vessels protector, Antimicrobial
Almond
Prunus dulcis
Hulls
Triterpenes (olcanoic, ursolic, betulinic acids), daucosterol
Anticancer
Hazelnut
Corylus avellana
Skins, hard shells, leafy covers
Phenolic acids (gallic, caffeic,
p
-coumaric, ferulic, sinapic)
Antioxidant
Chestnut
Castanea sativa
Shells (outer, inner)
Tannins, polyphenols, tocopherols
Antioxidant
Walnut
Juglans regia
Shells
Holocellulose, α-cellulose, lignin
Panel manufacture
Pecan nut
Carya illinoensis
Shells (endocarp)
Poly and monomeric phenols
Antifungal
Pistachio
Pistachia vera
Hulls
Phenolic compounds
Antioxidant
Legume industry
Pea
Pisum sativum
Husks
Growth factors (nitrogen and carbon)
Carrier for rhizobial inoculants
Pods
Fibre, polyphenols
Antioxidant, texturing additive
Faba bean
Vicia faba
Pods
Fibre, polyphenols
Antioxidant, texturing additive
Off-quality grains
Protein
Food ingredient
Chickpea
Cicer arietinum
Off-quality grains
Peptides
Metal chelating, antihypertensive, food ingredient
Common bean
Phaseolus vulgaris
Off-quality grains
Peptides
Antioxidant, metal chelating
Cereal industry
Rice
Oryza sativa
Rice brand
Tocotrienols-tocopherols, γ-oryzanol, β-sitosterol
Anticholesterol
Wheat
Triticum durum
Wheat brand
Vitamin E, carotenoids, quinines
Nutrients, antioxidant
Wine industry
Grape
Vitis vinifera
Stems
Betulinic acid, stilbenoid
trans
-resveratrol,
trans
-3-viniferin, sitosterol 6′-
O
-acylglucosides
Anticancer
Pomace
Flavonols, flavonols glucosides, flavanols, gallate esters, anthocyanins, proanthocyanins
Antioxidant, antimicrobial
Seeds
Epicatechin, caffeic and gallic acids
Antimicrobial
Brewing industry
Barley
Hordeum vulgare
Spent grains
Xylitol, cellulose, hemicelluloses, lignin, xylose, glucose, arabinose, protein, ferulic and
p
-coumaric acids
Growth medium, lactic acid production, diabetes treatment (xylitol)
Oil industry
Olive
Olea europaea
Olive mill wastewaters ‘alpechin’
Hydroxytyrosol, gallic acid, oleuropein, ligstroside isomers and derivatives, squalene, tocopherols, triterpenes, soluble sugars, polyphenols
Antimicrobial, antioxidant, anti-inflammatory, textile dyes
Pomace (solid wastes)
Hydroxytyrosol, tyrosol, caffeic protocatechuic, vanillic, p-coumaric and syringic acids, vanillin, oleuropein, apigenin
Antioxidant
Flesh, stones, seeds
Polyphenols, tocopherol
Antioxidants
Rapeseed
Brassica napus
Meals
Gallic and syringic acids, kaempferol, naringenin
Antioxidant, anti-inflammatory
Defatted cakes
Glucosinolates, peptides
Herbicide, food additive, foaming, emulsifying, anthitrombotic, antiviral
Turnip
Brassica rapa
Hulls, defatted cakes
Polyphenols
Antioxidant
Cotton
Gossypium hirsutum
Meals
Kaempferol, naringenin, rutin
Antioxidant, anti-inflammatory
Peanut
Arachis hypogeal
Defatted flours
Protein
Packaging biomaterials
Soybean
Glycine max
Meals
Caffeic acid, naringenin, daidzein
Antioxidant, anti-inflammatory
Sunflower
Helianthus annuus
Defatted cakes
Protein concentrates and isolates
Food ingredient
Peptides
Antihypertensive, anticholesterol
Essential oil industry (residues after distillation)
Lavandin
La
v
andula
×
intermedia
Solid residues
Phenolic acids, flavonoids, hydroxycinnamoylquinic acid derivatives, glucosides of hydroxycinnamic acids
Antioxidant
Rosemary
Rosmarinus officinalis
Solid residues
Phenolic acids (rosmarinic, carnosic, caffeic, chlorogenic acid and
p
-coumaric acids)
Antioxidant
Sage
Salvia officinalis, S. glutinosa
Solid residues
Coumarins, hydrocarbons, monoterpenes, phenolic compounds, sesquiterpenes, diterpenes, triterpenes, fatty acid ester, hydroxycinnamic acid, luteolin
Antimicrobial, antioxidant, textile dyes
Thyme
Thymus
v
ulgaris
Solid residues
Rosmarinic acid, hydroxycinnamic acid, luteolin
Antioxidant, textile dyes
Bay laurel
Laurus nobilis
Hydrolates
Terpinen-4-ol, α-terpineol, phenol
Antioxidant
Malt industry
Malt
Malt sprouts
Growth factors (nitrogen and carbon)
Carrier for rhizobial inoculant
Tuber processing industry
Potato
Solanum tuberosum
Peels
Proteins
Produce yeast biomass
Peels
Glycoalkaloids
Pesticide, anticancer
Wood industry
Pine
Pinus
sp.
Vinegars
Aldehydes, ketones, acids, esters, phenols (cresols)
Repellent, insecticide, herbicide,
Bark
Polyphenols
Antioxidant, anti-inflammatory
Other industrial crops
Sisal
Agave sisalana
Waste liquids (juice)
Saponins, glycosides, terpenoids, tannins
Antimicrobial
Cork oak
Quercus suber
Black waxes
Friedelane triterpenes (friedelin, 3-hydroxyfriedel-3-en-2-
one
), β-sitosterol, campesterol, α-amyrin, sitost-4-en-3-
one
Antiinflammatory, antibacterial, antifungal, antiviral, cytotoxic, insecticidal
Cassava
Manihot esculenta
Bagasse
Starch
Carbon source for microbial growth
Sugarcane industry
Sugarcane
Saccharum officinarum
Bagasse
α-cellulose, pentosans
Enzyme production
Tobacco industry
Tobacco
Nicotiana tabacum
Stems, leaves
Mono-caffeoylquinic acids
Antibacterial, antioxidant, anti-hyperglycemic antimutagenic
Sugar cane had the highest production globally (1910 million tonnes), followed by maize, rice, wheat, potatoes, fresh vegetable, cassava, soybeans, palm fruit and sugar beet (1020, 741, 716, 376, 280, 277, 276, 266 and 247 million tonnes, respectively) (Table 1.2). All of these crops produced a large amount of relevant wastes, including leaves, tops and bagasse from sugar cane; straw, stalks, husk, bran and cobs from maize, rice and wheat; foliage, tops, peels and pulps from potatoes; leaves, stems, peels, skins and seeds from fresh vegetables; and peels, stalks and bagasse from cassava (FAOSTAT, 2015).
The wastes from crop-based residues, in terms of aerial biomass, roots, leaves, straw and stems, are rich sources of bioactive compounds, including polyphenols, flavonoids, sterols, anthocyanins and carbohydrates, which have direct links with potent pharmacological properties, such as antioxidant, antibacterial, antifungal, antimicrobial, anti-inflammatory and anticholesterol capacity (Table 1.3). Many valuable bioactive compounds, such as glycosides, procyanidins, proanthocyanidins, flavonols, flavanols, flavonoids, phenolic acids, carotenoids, saponins, tannins, alkaloids, steroids, triterpenes, quinones and peptides, can also be isolated from processing-based residues, such as from the fresh fruit, dry fruit, brewing, wine, cereal, oil, essential oil, sugarcane and tobacco industries (Table 1.4). The bioactive compounds isolated from these sources have been proved to possess a wide range of biological activities, including antioxidant, anticancer, antidiarrhoeal, antibacterial, antifungal, antiviral, antimicrobial, antihypertensive, antimutagenic, anti-inflammatory and anticholesterol properties (Santana-Méridas et al., 2012).
Phenolic compounds, found ubiquitously in plants, are an essential part of the human diet. They are also of considerable interest due to their antioxidant properties. The phenolic compounds possess an aromatic ring bearing one or more hydroxyl groups and their structures range from that of a simple phenolic molecule to that of a complex high-molecular weight polymer. The chemical structures of hydroxybenzoic and hydroxycinnamic acids (gallic acid, protocatechuic acid, ρ-coumaric acid, caffeic acid, ferulic acid and sinapic acid) are shown in Figure 1.2, while Figure 1.3 indicates the chemical structures of major classes of flavonoids (flavone, flavonol, flavanone, flavanol and anthocyanidin) (Balasundram et al., 2006).
Figure 1.2 Chemical structures of (a) hydroxybenzoic and (b) hydroxycinnamic acids.
Source: Balasundram (2006). Reproduced with permission of Elsevier.
Figure 1.3 Chemical structures of major classes of flavonoids.
Source: Balasundram (2006). Reproduced with permission of Elsevier.
Table 1.5 shows the phenolic compounds, such as phenolic acids, flavonols, flavanols, flavonoids and anthocyanins, obtained from agricultural byproducts, such as the hulls of rice, buckwheat, almond, Swedish oats and pistachio; the peels and seeds of citrus, lemons, oranges and grapefruit; the peels of apples, peaches, pears, flesh nectarines, pomegranate and bananas; apple pomace; olive mill wastewater (OMW) and leaves; grape seeds and skin; the seeds of mango, longan, avocado and jackfruit; the peels and seeds of tomatoes; and pineapple waste (residual pulp, peels and skin) (Balasundram et al., 2006).
Table 1.5 Phenolic compounds from agricultural byproducts. Source: Balasundram (2006). Reproduced with permission of Elsevier
Byproduct
Phenolic compounds
Levels
a
Almond (
Prunus dulcis
(Mill.) D.A. Webb) hulls
Chlorogenic acid
42.52 ± 4.50 mg/100 g fw
4-
O
-caffeoylquinic acid
7.90 mg/100 g fw
3-
O
-caffeoylquinic acid
3.04 mg/100 g fw
Apple peels
Flavonoids
2299 mg CE/100 g dw
Anthocyanin
169 mg CGE/100 g dw
Artichoke blanching waters
Neochlorogenic acid
11.3 g phenolics/100 ml
Cryptochlorogenic acid
Chlorogenic acid
Cynarin
Caffeic acid derivatives
Buckwheat (
Fagopyrum esculentum
Möench) hulls
Protocatechuic acid
13.4 mg/100 mg dw
3,4-dihydroxybenzaldehyde
6.1 mg/100 g dw
Hyperin
5.0 mg/100 g dw
Rutin
4.3 mg/100 g dw
Quercetin
2.5 mg/100 g dw
Dried apple pomace
Flavonols
673 mg/kg dw
Flavanols
318 mg/kg dw
Dihydrochalcones
861 mg/kg dw
Hydroxycinnamatcs
562 mg/kg dw
Dried coconut husk
4-hydroxybenzoic acid ferulic acid
13.0 mg phenolics/g dry weight
a Expressed on fresh weight (fw) or dry weight (dw) basis.
Among the phenolic compounds derived from agricultural byproducts (Table 1.5), hydroxytyrosol, tyrosol, oleuropein and hydroxycinnamic acids are the major components of OMW, while oleuropein is the major component of olive leaves, followed by hydroxytyrosol, luteolin-7-glucoside, apigenin-7-glucoside and verbascoside. Apple peel is rich in flavonoids (approximately 23 mg catechin equivalents/g dry weight), while dried coconut husk contains a high amount of 4-hydroxybenzoic acid (13.0 mg phenolics/g dry weight).
In recent years, a number of studies have been conducted to recover the bioactive compounds from various agricultural wastes. Table 1.6 illustrates a wide range of traditional and emerging techniques that have been applied to the extraction and isolation of valuable bioactive compounds from food wastes, such as solid–liquid extraction (SLE), ultrasound-assisted extraction (UAE), microwave-assisted extraction (MAE), supercritical fluid extraction (SFE), high hydrostatic pressure (HHP), pulsed electric fields (PEF) and membrane and resin techniques. These techniques allow high yields of bioactive compounds to be achieved, such as pectin (10–30%), flavanones, soluble dietary fibres (10%), phenolic compounds (33%), lycopene and β-carotene (50%), anthocyanins, caffeine (97%), essential oils (matricine, chamazulene and α-bisabolol: 28.08, 0.05 and 2.68%, respectively), capsaicinoids and colour components (66–86% and 26–34%, respectively), γ-oryzanol (1527–4164 mg/kg), β-glucans, lignans, phenolic acids, tocopherols, tocotrienols, sterols and squalene (Baiano, 2014).
Table 1.6 Molecule of interest, substrate from food wastes, extraction method and yield. Source: Baiano (2014), http://www.mdpi.com/1420-3049/19/9/14821/htm. Used under CC BY 3.0 https://creativecommons.org/licenses/by/3.0/
Extractable biomolecule
Substrate
Extraction method
Yield
Pectin
Apple pomace,citrus peel, sugar beet, sunflower heads, wastes from tropical fruits
Solid–liquid extraction
10–15%, 20–30%
Flavanones
Citrus peels and residues from segments and seeds after pressing
Solid–liquid extraction
Total and soluble dietary fibres
Apple pomace
Solid–liquid extraction
72 and 10%
Phenolic compounds
Apple pomace
Solid–liquid extraction
33%
Lycopene and β-carotene
Tomato pomace
Supercritical CO
2
50%
Anthocyanins
Grape skins
Heat treatment at 70 °C, Ultrasonics, high hydrostatic pressure, pulsed electric fields
Variable
Caffeine
Green tea leaves
Supercritical fluid extraction
97%
Essential oils (matricine, chamazulene and α-bisabolol
Chamomile
Supercritical fluid extraction
28.08, 0.05 and 2.68%, respectively
Capsaicinoids and colour components
Chilli pepper
Supercritical fluid extraction
66–86% and 26–34%, respectively
Oil
Rice bran
Supercritical fluid extraction
24.65%
γ-oryzanol
Rice bran
Solid–liquid extraction
1527–4164 mg/kg
β-glucans
Barley bran
Solid–liquid extraction
Lignans
Flaxseeds
Solid–liquid extraction
Phenolic acids
Wheat brans
Solid–liquid extraction, ultrasound-assisted extraction, microwave-assisted extraction
Tocopherols, tocotrienols, sterols, and squalene
Palm fatty acid distillate
Liquid–liquid extraction
Phenolic antioxidants
Aqueous byproducts from the palm oil extraction
Separation techniques through membranes
Tocopherols and tocotrienols
Palm fatty acid distillate
Treatment with alkyl alcohol and sodium methoxide; distillation under reduced pressure; a cooling step; passage of the filtrate through an ion-exchange column with anionic exchange resin; removal of the solvent; molecular distillation
Phenolic antioxidants
Aqueous byproducts from the extraction of palm oil
Without solvent; based on simple separation principles
Table 1.7 describes the use of different solvents to obtain high yields of bioactive compounds and shows individual bioactive compounds in extracts from agro-industrial wastes, while Table 1.8 shows the antioxidant activity of extracts from agro-industrial residues (Moure et al., 2001). Perretti et al. (2003) extracted α-tocopherol and γ-oryzanol from rice byproducts (hulls, rice bran) using SFE and found that the γ-oryzanol content ranged from 8.2 to 18.0 mg/kg, while the α-tocopherol content was greatly affected by extraction conditions in terms of pressure and temperature (1176.9 and 1228.1 mg/kg at 5000 psi/40 °C and 10 000 psi/80 °C, respectively). Kim et al. (2006) reported that extracts from cereal brans possessed stronger antioxidant activity than free phenolic acids, with ferulic, vanillic and syringic acids found to be the major individual phenolic acids in wheat bran. Izydorczyk & Dexter (2008) found that β-glucans extracted from barley flour could improve lipid metabolism, reduce glycaemic index, lower plasma cholesterol and reduce risk of colon cancer, while Zanwar et al. (2011) reported biological activity of lignan concentrates from flaxseed as anticancer, antioxidant, antibacterial, antiviral and anti-inflammatory agents.
Table 1.7 Extraction yields, total extractable polyphenols (TEP) and composition of crude extracts from agro-industrial wastes. Source: Moure et al. (2001). Reproduced with permission of Elsevier
Residue
Solvent
Solubles yield (% dry weight) or TEP (as equivalents)
Identified compounds
Durum wheat bran
Ethanol
12.1 (% dry weight) 2.769 (HPLC)
PA, pBA, GA, CaA, VA, CA, SA, pCA, FA
Fraxinus ornus
bark
Ethanol
14.5 (dry weight)
Hydroxycoumarin (Es, Est, Fx, Fxt)
Corn bran hemicelluloses
NaOH
