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Bio-pigmentation and Biotechnological Implementations [Hardback]

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  • Formāts: Hardback, 312 pages, height x width x depth: 246x173x18 mm, weight: 816 g
  • Izdošanas datums: 28-Jul-2017
  • Izdevniecība: Wiley-Blackwell
  • ISBN-10: 1119166144
  • ISBN-13: 9781119166146
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  • Formāts: Hardback, 312 pages, height x width x depth: 246x173x18 mm, weight: 816 g
  • Izdošanas datums: 28-Jul-2017
  • Izdevniecība: Wiley-Blackwell
  • ISBN-10: 1119166144
  • ISBN-13: 9781119166146
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"Provide the insights of bio-pigmentation and molecular mechanisms of microbial biosynthesis of pigments. The new avenues of bio-pigments as sustainable resources to overcome from chemically synthesized pigments under safety net will be established"--Provided by publisher.

Biological pigments are naturally occurring chemical compounds which appear as color and serve a variety of functional purposes such as absorbing ultra violet (UV) light in order to promote photosynthesis, desorbing certain UV wavelengths to protect organisms from photo damage, or to oblige as an attraction to other organisms in order to promote mating or pollination. The visual character of pigmentation also serves to be an indicator of quality. Color based evaluation is essential as it indicates fertility, nutritional value, flavor, toxicity, or spoilage in food. Human society has incorporated this knowledge of the instinctive perception of color into marketing by increasing the appeal of food items, pharmaceuticals, and cosmetics.

Both artificial food colors (AFCs) or synthetic pigments and natural pigments are used as color additives to augment or correct imperfections of a food’s natural color, indicate artificially flavored foods and medicines, or serve as decorative purpose. The color additives are being used to provide color to foods whose natural color would potentially degrade through shipment and storage when exposed to UV light, extreme changes in temperature or humidity. In these cases, artificial color additives whose chemical structures are stable and do not degrade under various conditions can be preferable for marketing purposes.

However, the quandary lies directly in the advantage of chemically stable compounds. Naturally occurring pigments are biological derivatives of organic compounds, which can be metabolically or chemically broken down because they serve to synchronize with organismal demands (Shindo and Misawa 2013; Oren, 2013). Whereas the artificial chemical colors are the derivatives of coal-tar and petroleum, which cannot be degraded completely. Therefore artificial pigments are potentially perilous to life because such chemical behaviors are asynchronous with biological function. Studies have shown how various AFCs are being linked to biological and neurological effects, such as contributing to attention deficit hyperactivity (ADHD) behaviors in children, affecting nutrient absorption and metabolism, and cancer (Arnold et al., 2012; Kobylewski and  Jacobson 2012; Sonuga-Barke et al., 2013; Lok et al., 2013; Smith et al., 2015; Vojdani and Vojdani, 2015).

The United States Food and Drug Administration’s (US FDA) under FD&C Act,” (Food, Drugs and Cosmetics Act), Title 21 of the Code of Federal Regulations (CFR) has approved use of color additives in food, and regarded as “GRAS” (Generally Recognized as Safe) (http://www.fda.gov/ForIndustry/ColorAdditives/default.htm;
http://www.fda.gov/Food/IngredientsPackagingLabeling/GRAS/)
. The “safe” amount of an artificial color known as the acceptable daily intake (ADI), measured in parts per million (ppm) that industries are legally permitted to use in products. However, if organisms, specifically humans and animals, cannot metabolize artificial chemical compounds how much of a dose considered as “safe” for consumption remains questionable.

As the development and creation of new technologies continues to thrive and be advantageous to comprehensive human society, the increasing demand for natural alternatives of artificial coloring can be fulfilled. The biological pigments such as carotenoids, xanthophylls (i.e. b-carotene, lycopene, lutein, canthaxanthine, rhodoxanthin, astaxanthin, zeaxanthin, phycocyanin, monascin), violacein, and melanins for industrial applications in the food, pharmaceutical, and cosmetic industries are gaining great attention (Mata-Gomez et al, 2014; Bhosale and Bernstein, 2005; Stahl and Sies, 2005). Chromobacterium violaceum is a Gram-negative proteobacteria found in the soil and water in tropical and subtropical environments. The bacterium is able to live under anaerobic and aerobic conditions but violacein as pigment only occurs in aerobic condition. Violacein is a secondary metabolite and has great potential for pharmacological applications such as antibacterial, anti-trypanocidal, anit-ulcerogenic, and anticancer drug (Hoshino, 2011; Vaishnav and Demain, 2011; Duran et al., 2010;  Duran et al., 2007). Another well-studied bacterial pigment is prodigiosin, a bright red colored bacterial pigment produced by wide variety of bacterial taxa, including Gram-negative rods such as S. rubidaea, Vibrio gazogenes, Alteromonas rubra, Rugamonas rubra, and Gram-positive actinomycetes, such as Streptoverticillium rubrireticuli and Streptomyces longisporus. Prodigiosin has been proved to be effective as anti-microbial, anti-malarial, anti-cancer and immunosuppressive pigment. In vitro, prodigiosins have been shown to primarily target the cancer cells independently of the p53 status while little or no effect has been observed on normal cells. In addition, prodigiosins are effective in cancer cells with multidrug resistance phenotype and defects in the apoptotic pathways (Pandey et al., 2009; Vaishnav and Demain, 2011; Chang et al., 2011).

The unique microbial metabolic pathways in which bio-pigments are being synthesized could be the most appropriate methodologies to develop as safest form of natural pigmentation in industries. Understanding the genetic sequences for the biosynthetic metabolites provides further insight as to how genes can be manipulated in microorganisms to obtain higher yields of specific biological pigments.The broader impact of bio-pigments from microorganisms will implement these compounds into food science, pharmacology, and biomedical practices.

This project aims to introduce the basics and advancements made thus far in the biochemistry and bioprocessing of various bio-pigmentation from microorganisms (i.e. bacteria and fungi) as well as their implementation in biotechnology and therapeutics. The main aims are to (a) introduce readers to the wide variety of microorganisms (i.e. bacteria and fungi) and their capability of pigment production, (b) provide an overview of the methodologies applied to screen and identify the pigment producing microorganisms, (c) provide a literature review on diversity of pigment producing microorganisms, (d) discuss the molecular mechanism of pigment biochemistry in microorganisms, (e) discuss the use of bio-pigments in food feed and pharmaceutical industries, (f) discuss the regulations, challenges and implications of enforcements from regulatory agencies. These aims will be organized by invited research/ review articles from renowned researchers exploring bio-pigmentation among variety of microorganisms (i.e. bacteria and fungi), and differ in length and number of chapters, with the literature review section containing the bulk of the text.

The reader should first be enticed to read this book because of the extensive use of colors in food and related products as well as their usage in pharmaceutical industries (e.g. antibacterial, anti-trypanocidal, anti-ulcerogenic, and anticancer drug). There are positive and negative aspects of food alteration in relation to the artificial coloring. Among positives, seafood such as salmon fish and dairy product such as cheese, yogurt is being tied with human consumption; whereas negative aspects are seen in the color stabilization and accumulation in the environment. The biochemical pathways in which several derivatives of carotenoids and/or prodigiosin including other pigments being observed are equally important to address towards strengthen the promises of stable coloration in microbial factories.

The second section introduces the methodologies to explore the diversity of microorganisms from variety of sources including soil, plants and animals. The role of microbial adaptability under extreme conditions has been reported to reveal specific coloration in various microorganisms intra and extra-cellularly. The concept of this section will address to compare the different methodologies for color production and extraction. These methodologies may provide a common ground towards a feasible approach of coloration in food, feed, and pharmaceuticals.

The third section will review the literature based historical perspectives of color producing microorganisms making emphasis of established research into open market field of food and medical industries.

Food, feed and pharmaceutical coloration acts as a major source of wealth creation around the globe. Together with the third, fourth section will review the basic and current aspects of literature. The fourth section will rely on the information obtained from different methodologies and its interpretation of microorganisms and health initiatives. This section will be the longest as this section will have details of tools and methods adapted to screen and isolate variety of microorganisms, and discover new/ ideal ways to secure the food, feed and pharmaceutical coloration using bio-pigments. To enhance the color formation within microbial cells, the data interpretation towards translative research for industrial implication will further assist providing the clues of microbial metabolism in variety of growth medium under varying environmental conditions.

Systematic tools of systems biology (i.e. Genomics, Proteomics, and Metabolomics) are useful ways to identify how microorganisms respond to certain environmental factors. Understanding of stress responsive factors may reveal changes in the microbial metabolic networks as well as cellular responses (via gene and protein expression) among color producing microorganisms. In the fifth section, the interpretation of genomics and proteomics data, which has better capabilities, would significantly impact the core interest of this book. Further, the fifth section will also introduce the desired microbial traits and cloning of advantageous trait for microbial color production.

As regarded above, the US FDA under FD&C Act has approved use of color additives in food, feed and pharmaceuticals under GRAS category. The FDA names approved straight colors by FD&C prefix followed by a number. Some of these colors include FD&C Blue No.1, FD&C Blue No. 2, FD&C Green No.3, FD&C Red No.3, FD&C Red No.40, FD&C Yellow No. 5, and FD&C Yellow No. 6. Other color additives, such as Orange B an Citrus No. 40, are only approved for specific uses, such as enhancing the color of sausage casings and orange rinds, respectively. The interpretations of FDA’s stand on color additives will be discussed in the sixth section of this book exploring color regulations in the USA comparing to globally for safety of human and animal consumptions.

List of Contributors xv
Introduction xvii
1 Introduction Of Natural Pigments From Microorganisms 1(22)
Siyuan Wang
Fuchao Xu
Jixun Zhan
1.1 Introduction
1(1)
1.2 Microbial Pigments from Eukaryotic Sources
2(7)
1.2.1 Pigments from Algae
2(2)
1.2.2 Pigments from Fungi
4(3)
1.2.3 Pigments from Yeasts
7(2)
1.3 Natural Pigments from Prokaryotes
9(7)
1.3.1 Natural Pigments from Cyanobacteria
9(1)
1.3.2 Natural Pigments from Bacteria
10(6)
1.4 Conclusion
16(1)
References
16(7)
2 Establishing Novel Cell Factories Producing Natural Pigments In Europe 23(38)
Gerit Tolborg
Thomas Isbrandt
Thomas Ostenfeld Larsen
Mhairi Workman
2.1 Introduction
23(2)
2.2 Colorants
25(7)
2.2.1 Classification of Colorants
25(1)
2.2.2 Monascus Pigments
26(3)
2.2.3 Biosynthesis of Monascus Pigments
29(2)
2.2.4 Derivatives of Monascus Pigments
31(1)
2.3 Screening for Monascus Pigment-Producing Cell Factories for the European Market
32(2)
2.3.1 Cell Factory Selection and Identification
32(1)
2.3.2 From Single Pigment Producers to High-Performance Cell Factories
33(1)
2.4 Assessment of the Color Yield
34(7)
2.4.1 Pigment Purification and Quantification
34(3)
2.4.2 Detection and Identification
37(1)
2.4.3 Quantification
38(3)
2.4.4 CIELAB
41(1)
2.5 Optimizing Cellular Performance: Growth and Pigment Production
41(9)
2.5.1 Assessment of Classical Physiological Parameters
42(1)
2.5.2 Media Composition
42(2)
2.5.3 Cultivation Parameters
44(2)
2.5.4 Type of Cultivation
46(2)
2.5.5 Metabolic Engineering
48(2)
2.6 Pigment Properties
50(1)
2.7 Conclusion
51(1)
References
51(10)
3 Color-Producing Extremophiles 61(26)
Eva Garcia-Lopez
Alberto Alcazar
Ana Maria Moreno
Cristina Cid
3.1 Introduction
61(2)
3.2 Color-Producing Extremophiles 62.
3.2.1 Thermophiles and Hyperthermophiles
63(1)
3.2.2 Psychrophiles and Psychrotolerants
63(3)
3.2.3 Alkaliphiles
66(1)
3.2.4 Acidophiles
66(1)
3.2.5 Piezophiles and Piezotolerants
66(1)
3.2.6 Halophiles and Halotolerants
67(1)
3.2.7 Radiophiles
67(1)
3.3 Microbial Pigments
68(5)
3.3.1 Chlorophylls and Bacteriochlorophylls
68(1)
3.3.2 Carotenoids and Phycobilins
69(1)
3.3.3 Violacein
70(1)
3.3.4 Prodigiosin
70(1)
3.3.5 Pyocyanin
70(1)
3.3.6 Azaphilones
70(1)
3.3.7 Bacteriorhodopsin
71(1)
3.3.8 Cytochromes
71(1)
3.3.9 Other
72(1)
3.4 Biotechnological Applications of Microbial Pigments from Extremophiles
73(7)
3.4.1 Applications in the Food Industry
74(3)
3.4.2 Applications in the Pharmaceutical Industry
77(1)
3.4.3 Applications in the Textile Industry
78(1)
3.4.4 Applications as Laboratory Tools
78(1)
3.4.5 Applications in Bioremediation
79(1)
3.4.6 Development of Microbial Fuel Cells
79(1)
3.4.7 Biotechnological Production of Natural Pigments
80(1)
3.5 Conclusion
80(1)
Acknowledgments
80(1)
References
80(7)
4 Current Carotenoid Production Using Microorganisms 87(20)
Laurent Dufosse
4.1 Introduction
87(1)
4.2 beta-carotene
88(3)
4.2.1 B. trispora
88(2)
4.2.2 Phycomyces blakesleeanus
90(1)
4.2.3 Mucor circinelloides
91(1)
4.2.4 Applications
91(1)
4.3 Lyeopene
91(2)
4.3.1 B. trispora
92(1)
4.3.2 Fusarium sporotrichioides
93(1)
4.4 Astaxanthin
93(4)
4.4.1 X. dendrorhous, Formerly Phaffia rhodozyma
94(1)
4.4.2 Agrobacterium aurantiacum and Other Bacteria
95(1)
4.4.3 Advantages over Other Carotenoids
95(1)
4.4.4 Astaxanthin for Salmon and Trout Feeds
96(1)
4.4.5 Astaxanthin for Humans
97(1)
4.5 Zeaxanthin
97(1)
4.6 Canthaxanthin
98(1)
4.7 Torulene and Thorularhodin
99(1)
4.8 Prospects for Carotenoid Production by Genetically Modified Microorganisms
99(3)
4.8.1 Escherichia coli and Other Hosts
99(2)
4.8.2 Directed Evolution and Combinatorial Biosynthesis
101(1)
4.9 Conclusion
102(2)
References
104(3)
5 C50 Carotenoids: Occurrence, Biosynthesis, Glycosylation, And Metabolic Engineering For Their Overproduction 107(20)
Nadja A. Henke
Petra Peters-Wendisch
Volker F Wendisch
Sabine A.E. Heider
5.1 Introduction
107(1)
5.2 Occurrence and Biological Function of C50 Carotenoids
108(2)
5.3 Biosynthesis of C50 Carotenoids
110(4)
5.4 Glycosylation of C50 Carotenoids
114(1)
5.5 Overproduction of C50 Carotenoids by Metabolic Engineering
115(3)
5.6 Conclusion
118(1)
Acknowledgments
119(1)
References
119(8)
6 Biopigments And Microbial Biosynthesis Of beta-Carotenoids 127(34)
Rosemary C. Nwabuogu
Jennifer Lau
Om V. Singh
6.1 Introduction
127(2)
6.2 Characterization of Biological Pigments
129(4)
6.2.1 Tetrapyrrole Derivatives
129(1)
6.2.2 N-heterocyclic Derivatives
130(1)
6.2.3 Isoprenoid Derivatives
131(1)
6.2.4 Benzopran Derivatives
132(1)
6.2.5 Quinones
132(1)
6.2.6 Melanins
133(1)
6.3 Biosynthetic Routes of beta-carotene
133(13)
6.3.1 Fermentation of beta-carotene
138(8)
6.4 Molecular Regulation of beta-carotene Biosynthesis
146(1)
6.5 Commercialization of beta-carotene
147(4)
6.6 Conclusion
151(1)
References
151(10)
7 Biotechnological Production Of Melanins With Microorganisms 161(12)
Guillermo Gosset
7.1 Introduction
161(2)
7.2 Microbial Production of Melanins
163(2)
7.3 Production of Melanins with Engineered Microorganisms
165(4)
7.4 Conclusion
169(1)
References
170(3)
8 Biochemistry And Molecular Mechanisms Of Monascus Pigments 173(20)
Changlu Wang
Di Chen
Jiancheng Qi
8.1 Introduction
173(1)
8.2 Monascus Pigments
174(2)
8.3 The Properties of Monascus Pigments
176(1)
8.3.1 Solubility
176(1)
8.3.2 Stability
177(1)
8.3.3 Safety
177(1)
8.4 Functional Properties of Monascus Pigments
177(2)
8.4.1 Antimicrobial Activities
178(1)
8.4.2 Anti-inflammatory Activities
178(1)
8.4.3 Anti-obesity Activities
178(1)
8.4.4 Anticancer Activities
178(1)
8.5 Biosynthetic Pathway of Monascus Pigments
179(2)
8.6 Biosynthetic Pathway of Related Genes
181(3)
8.7 Factors Affecting Monascus Pigment Production
184(3)
8.7.1 Solid-State Fermentation
185(1)
8.7.2 Submerged Fermentation
186(1)
8.7.3 Carbon Source
186(1)
8.7.4 Nitrogen Source
187(1)
8.7.5 Temperature
187(1)
8.7.6 Light
187(1)
References
187(6)
9 Diversity And Applications Of Versatile Pigments Produced By Monascus SP 193(22)
Sunil H. Koli
Rahul K. Suryawanshi
Chandrashekhar D. Patil
Satish V. Patil
9.1 Introduction
193(2)
9.2 Pigment-Producing Monascus Strains
195(4)
9.3 Various Types of Monascus Pigments
199(4)
9.4 Extraction and Purification of Monascus Pigments
203(1)
9.5 Detection and Purification
204(2)
9.5.1 UV-Vis Spectrophotometric Methods
204(1)
9.5.2 Column Chromatography
204(1)
9.5.3 Thin-Layer Chromatography
205(1)
9.5.4 High-Performance Liquid Chromatography
205(1)
9.6 Applications
206(3)
9.6.1 Food Colorants
206(1)
9.6.2 Biological Role
206(3)
9.7 Conclusion
209(1)
Acknowledgments
209(1)
References
209(6)
10 Microbial Pigment Production Utilizing Agro-Industrial Waste And Its Applications 215(26)
Chidambaram Kulandaisamy Venil
Nur Zulaikha Binti Yusof Claira Arul Aruldass
Wan Azlina Ahmad
10.1 Introduction
215(1)
10.2 Agro-industrial Waste Generation: A Scenario
216(1)
10.3 Microbial Pigments
216(7)
10.4 Production of Microbial Pigments Utilizing Agro-industrial Waste from Different Industries
223(2)
10.5 Case Study: Production of Violacein by Chromobacterium violaceum Grown in Agricultural Wastes
225(10)
10.5.1 Introduction
225(1)
10.5.2 Materials and Methods
226(3)
10.5.3 Results and Discussion
229(6)
10.6 Conclusion
235(1)
Acknowledgments
235(1)
References
235(6)
11 Microbial Pigments: Potential Functions And Prospects 241(22)
P. Akilandeswari
B.V. Pradeep
11.1 Introduction
241(3)
11.1.1 Pigments
242(1)
11.1.2 Types of Pigments
242(1)
11.1.3 Microbial Pigments
242(1)
11.1.4 Use of Pigments
243(1)
11.1.5 Advantages of Natural Pigments
243(1)
11.1.6 Disadvantages of Synthetic Dyes
243(1)
11.2 Potential Sources of Microbial Pigments
244(2)
11.2.1 Actinomycetes
244(1)
11.2.2 Bacteria
245(1)
11.2.3 Fungi
245(1)
11.3 Physical Factors Influencing Microbial Pigments
246(1)
11.4 Chemical Factors Influencing Microbial Pigments
247(1)
11.5 Fermentation Practices in Pigment Production
248(1)
11.5.1 Solid-State Fermentation
248(1)
11.5.2 Submerged Fermentation
248(1)
11.6 Characterization and Purification Analysis
249(1)
11.7 Biocolors from Microbes and their Potential Functions
250(1)
11.7.1 Pharmaceutical Industry
250(7)
11.7.2 Food Colorants
255(1)
11.7.3 Textile Dyeing
256(1)
References
257(6)
12 The Microbial World Of Biocolor Production 263(16)
Roshan Gul
Raman Kumar
Anil K. Sharma
12.1 Introduction
263(2)
12.2 Pigments Produced by Microorganisms
265(1)
12.3 Classification of Pigments
265(4)
12.3.1 Riboflavin
265(1)
12.3.2 beta-carotene
265(3)
12.3.3 Canthaxanthin
268(1)
12.3.4 Carotenoids
268(1)
12.3.5 Prodigiosin
268(1)
12.3.6 Phycocyanin
268(1)
12.3.7 Violacein
268(1)
12.3.8 Astaxanthin
268(1)
12.4 Benefits and Applications of Microbial Pigments
269(3)
12.5 Conclusion
272(1)
References
273(6)
Index 279
Om V. Singh, PhD, is an Associate Professor of Microbiology at the University of Pittsburgh, Bradford, PA, USA. Dr. Singh's work in the field of microbiology and proteomics has focused on topics in environmental microbiology, bioenergy, stress proteins, and diversity of extremophiles, all areas in which he has published extensively over the decade.