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Biopolymers for Biomedical and Biotechnological Applications


Biopolymers for Biomedical and Biotechnological Applications


Advanced Biotechnology 1. Aufl.

von: Bernd H. A. Rehm, M. Fata Moradali

142,99 €

Verlag: Wiley-VCH
Format: PDF
Veröffentl.: 13.11.2020
ISBN/EAN: 9783527818280
Sprache: englisch
Anzahl Seiten: 400

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Beschreibungen

Provides insight into biopolymers, their physicochemical properties, and their biomedical and biotechnological applications <br> <br> This comprehensive book is a one-stop reference for the production, modifications, and assessment of biopolymers. It highlights the technical and methodological advancements in introducing biopolymers, their study, and promoted applications.<br> <br> "Biopolymers for Biomedical and Biotechnological Applications" begins with a general overview of biopolymers, properties, and biocompatibility. It then provides in-depth information in three dedicated sections: Biopolymers through Bioengineering and Biotechnology Venues; Polymeric Biomaterials with Wide Applications; and Biopolymers for Specific Applications. Chapters cover: advances in biocompatibility; advanced microbial polysaccharides; microbial cell factories for biomanufacturing of polysaccharides; exploitation of exopolysaccharides from lactic acid bacteria; and the new biopolymer for biomedical application called nanocellulose. Advances in mucin biopolymer research are presented, along with those in the synthesis of fibrous proteins and their applications. The book looks at microbial polyhydroxyalkanoates (PHAs), as well as natural and synthetic biopolymers in drug delivery and tissue engineering. It finishes with a chapter on the current state and applications of, and future trends in, biopolymers in regenerative medicine.<br> <br> * Offers a complete and thorough treatment of biopolymers from synthesis strategies and physiochemical properties to applications in industrial and medical biotechnology<br> * Discusses the most attracted biopolymers with wide and specific applications<br> * Takes a systematic approach to the field which allows readers to grasp and implement strategies for biomedical and biotechnological applications<br> <br> "Biopolymers for Biomedical and Biotechnological Applications" appeals to biotechnologists, bioengineers, and polymer chemists, as well as to those working in the biotechnological industry and institutes.<br>
<p><b>1 Advances in Biocompatibility: A Prerequisite for Biomedical Application of Biopolymers </b><b>1<br /></b><i>Matthew R. Jorgensen, Helin Räägel, and Thor S. Rollins</i></p> <p>1.1 Introduction 1</p> <p>1.2 Biocompatibility Evaluation of Biopolymeric Materials and Devices 2</p> <p>1.3 Using a Risk-Based Approach to Biocompatibility 4</p> <p>1.3.1 Chemistry of Biopolymers and Risk 6</p> <p>1.3.2 Chemistry Screening of Biopolymers 7</p> <p>1.4 Specific Biological Endpoint Evaluations 11</p> <p>1.4.1 Cytotoxicity 11</p> <p>1.4.2 Systemic Toxicity (Acute, Subacute, Subchronic, and Chronic) 12</p> <p>1.4.3 Implantation 14</p> <p>1.5 Conclusion 15</p> <p>References 16</p> <p><b>2 Advanced Microbial Polysaccharides </b><b>19<br /></b><i>Filomena Freitas, Cristiana A.V. Torres, Diana Araújo, Inês Farinha, João R. Pereira, Patrícia Concórdio-Reis, and Maria A.M. Reis</i></p> <p>2.1 Introduction 19</p> <p>2.2 Functional Properties and Applications of Microbial Polysaccharides 20</p> <p>2.3 Commercially Relevant Microbial Polysaccharides: Established Uses and Novel/Prospective Applications 22</p> <p>2.3.1 Pullulan 22</p> <p>2.3.2 Scleroglucan 23</p> <p>2.3.3 Xanthan Gum 23</p> <p>2.3.4 Dextrans 24</p> <p>2.3.5 Curdlan 24</p> <p>2.3.6 Gellan Gum 24</p> <p>2.3.7 Levan 25</p> <p>2.3.8 Hyaluronic Acid 25</p> <p>2.4 Hydrogels Based on Microbial Polysaccharides 25</p> <p>2.5 Bionanocomposites Based on Microbial Polysaccharides 29</p> <p>2.6 Bioactive Polysaccharides from Microalgae: An Emerging Area 32</p> <p>2.6.1 Polysaccharide-Producing Microalgae 33</p> <p>2.6.2 Biological Activity and Potential Applications 33</p> <p>2.6.2.1 Antiviral Activity 36</p> <p>2.6.2.2 Immunomodulatory, Anti-inflammatory, and Anticancer Activities 36</p> <p>2.6.2.3 Anticoagulant and Antithrombotic Activity 38</p> <p>2.6.2.4 Antioxidant Activity 38</p> <p>2.6.2.5 Other Biological Properties 39</p> <p>2.6.3 Commercialization Prospects 39</p> <p>2.7 Applications of Chitinous Polymers 40</p> <p>2.7.1 Chitin, Chitosan, and Chitinous Polysaccharides 40</p> <p>2.7.2 Properties of Chitinous Polysaccharides 41</p> <p>2.7.3 Applications of Chitinous Polysaccharides 41</p> <p>2.7.3.1 Biomedical Applications 42</p> <p>2.7.3.2 Pharmaceutical Applications 43</p> <p>2.7.3.3 Food Applications 43</p> <p>2.7.3.4 Other Applications 43</p> <p>2.8 Microbial Polysaccharides: A World of Opportunities 44</p> <p>Acknowledgments 45</p> <p>References 45</p> <p><b>3 Microbial Cell Factories for Biomanufacturing of Polysaccharides </b><b>63<br /></b><i>M. Fata Moradali and Bernd H.A. Rehm</i></p> <p>3.1 Introduction 63</p> <p>3.2 Prominent Microbial Polysaccharides and Their Properties and Applications 63</p> <p>3.2.1 Xanthan and Acetan 64</p> <p>3.2.2 Succinoglycan and Galactoglucan 64</p> <p>3.2.3 Sphingan Polysaccharides 66</p> <p>3.2.4 Pullulan 66</p> <p>3.2.5 Cellulose and Curdlan 67</p> <p>3.2.6 Alginates 67</p> <p>3.2.7 Hyaluronic Acid or Hyaluronate 68</p> <p>3.2.8 Dextrans 68</p> <p>3.2.9 Levan and Inulin 69</p> <p>3.3 Biosynthesis Pathways of Bacterial Polysaccharides 69</p> <p>3.3.1 Genetic Background Required for Biosynthesis of Polysaccharides in Bacteria 70</p> <p>3.3.2 Production of Active Precursor, Polymerization, and Polysaccharide Modifications 71</p> <p>3.3.3 Regulatory Pathways and Posttranslational Modifications 72</p> <p>3.4 Strategies for Engineering Cell Factories 76</p> <p>3.4.1 Enhancement of Productivity upon the Energetic State of the Cell and Metabolites 77</p> <p>3.4.2 Genetic and Metabolic Engineering of Cell Factories 78</p> <p>3.4.3 Strategies for Optimizing Physicochemical Properties of Polysaccharides 79</p> <p>3.4.4 Recombinant Production of Polysaccharides and Tailor-Made Products 83</p> <p>3.5 Conclusion and Future Perspective 86</p> <p>Acknowledgments 87</p> <p>References 87</p> <p><b>4 Exploitation of Exopolysaccharides from Lactic Acid Bacteria </b><b>103<br /></b><i>Tsuda Harutoshi</i></p> <p>4.1 Introduction 103</p> <p>4.1.1 Lactic Acid Bacteria 103</p> <p>4.1.2 Exopolysaccharides 103</p> <p>4.1.3 Importance of PS Produced by LAB 105</p> <p>4.2 Homo-PS 105</p> <p>4.2.1 Biosynthesis 105</p> <p>4.2.2 Composition and Structure 106</p> <p>4.2.3 Instability of Homo-PS Production 106</p> <p>4.3 Hetero-PS 111</p> <p>4.3.1 Biosynthesis 111</p> <p>4.3.2 Monosaccharides Composition of Hetero-PS 111</p> <p>4.3.3 Yield of Hetero-PS 112</p> <p>4.3.4 Instability of Hetero-PS Production 116</p> <p>4.4 Prebiotic Activity 117</p> <p>4.4.1 Commercial Prebiotic Oligosaccharides 117</p> <p>4.4.2 Prebiotic Polysaccharides 118</p> <p>4.4.3 Prebiotics in Japanese FOSHU 119</p> <p>4.4.4 Prebiotics Produced by LAB 119</p> <p>4.5 Conclusion 120</p> <p>References 120</p> <p><b>5 Nanocellulose: A New Biopolymer for Biomedical Application </b><b>129<br /></b><i>Hippolyte Durand, Megan Smyth, and Julien Bras</i></p> <p>5.1 Trends of Biobased Polymers in Biomedical Application 129</p> <p>5.1.1 Introduction to Biomedical Engineering 130</p> <p>5.1.2 Overview of Biobased Materials for Biomedical Applications 132</p> <p>5.1.2.1 Biomaterials: A Definition 132</p> <p>5.1.2.2 Biobased Polymers 135</p> <p>5.1.2.3 Cellulose as a Biomaterial 138</p> <p>5.2 Nanocellulose: Production, Characterization, Application, and Commercial Aspects 142</p> <p>5.2.1 Isolation and Characterization of Nanocellulose Materials 143</p> <p>5.2.1.1 Cellulose Nanocrystals 144</p> <p>5.2.1.2 Cellulose Nanofibrils 145</p> <p>5.2.1.3 Bacterial Nanocellulose (BNC) 149</p> <p>5.2.2 Characterization of Cellulosic Nanomaterials (CNMs) 151</p> <p>5.2.3 Industrialization of Nanocellulose: First and Upcoming Applications 153</p> <p>5.2.4 Health and Toxicology: A Concern for CNM Development in Biomedical Field 154</p> <p>5.2.5 Cellulose Nanofibrils and Medical Applications 164</p> <p>5.3 Conclusions and Perspectives 170</p> <p>References 170</p> <p><b>6 Advances in Mucin Biopolymer Research: Purification, Characterization, and Applications </b><b>181<br /></b><i>Matthias Marczynski, Benjamin Winkeljann, and Oliver Lieleg</i></p> <p>6.1 Introduction 181</p> <p>6.2 Mucin Sources and Purification Process 182</p> <p>6.3 Structure–Function Relation of Mucins 185</p> <p>6.4 Characterizing Mucins and Mucin-Based Materials 187</p> <p>6.5 Biomedical Applications of Purified Mucins 190</p> <p>6.5.1 Eye Drops or Contact Lens Coatings 190</p> <p>6.5.2 Mouth Sprays 192</p> <p>6.5.3 Artificial Joint Fluids 192</p> <p>6.5.4 Coatings of Medical Devices 193</p> <p>6.5.5 Components of Hydrogels for Drug Delivery 194</p> <p>6.5.6 Molecular Standards for Lab Tests with Clinical Mucus Samples 194</p> <p>6.6 Outlook: Engineered Mucins and Mucin-Mimetic Polymers 194</p> <p>Acknowledgments 195</p> <p>References 195</p> <p><b>7 Advances in the Synthesis of Fibrous Proteins and Their Applications </b><b>209<br /></b><i>Gang Wei, Xi Ma, Yaru Bai, Coucong Gong, and Yantu Zhang</i></p> <p>7.1 Introduction 209</p> <p>7.2 Synthesis, Structure, and Characterizations of Fibrous Protein Materials 210</p> <p>7.2.1 Synthesis Methods 210</p> <p>7.2.2 Structure 212</p> <p>7.2.3 Characterizations 213</p> <p>7.3 Applications of Fibrous Protein Materials 213</p> <p>7.3.1 Bone Tissue Engineering 213</p> <p>7.3.2 Biomedical Engineering 215</p> <p>7.3.3 Sensors and Biosensors 216</p> <p>7.3.4 Nanodevices 217</p> <p>7.3.5 Energy Application 218</p> <p>7.3.6 Environmental Application 220</p> <p>7.4 Conclusions 223</p> <p>Acknowledgments 224</p> <p>References 224</p> <p><b>8 Microbial Polyhydroxyalkanoates (PHAs): From Synthetic Biology to Industrialization </b><b>231<br /></b><i>Yuki Miyahara, Ayaka Hiroe, Shunsuke Sato, Takeharu Tsuge, and Seiichi Taguchi</i></p> <p>8.1 Introduction 231</p> <p>8.2 Synthetic Biology for Production of Kaneka PHBH 233</p> <p>8.2.1 Isolation of Bacterium Producing Poly(3-hydroxybutyrate-<i>co</i>-3-hydroxyhexanoate) 233</p> <p>8.2.2 Material Properties of PHBH 234</p> <p>8.2.3 Industrial PHBH Production Process 235</p> <p>8.2.4 Molecular Breeding of PHBH-Producing Bacteria 236</p> <p>8.2.5 Precise Control of 3HHx Fraction by Genetic Modification of <i>Ralstonia eutropha </i>238</p> <p>8.2.6 Business Plan for Kaneka PHBH Industrialization 239</p> <p>8.3 Synthetic Biology for Production of Medium-Chain-Length PHAs with Homogeneous Side-Chain Lengths (Homo-PHAs) 240</p> <p>8.3.1 Copolymers Based on Medium-Chain-Length PHA Monomeric Constituents 240</p> <p>8.3.2 Pathway Engineering for Homo-PHA Production 242</p> <p>8.3.3 Improved Microbial Production of Homo-PHAs 243</p> <p>8.3.4 Material Properties of Homo-PHAs 245</p> <p>8.3.5 Integrated Production Process of Homo-PHAs from Renewable Feedstock 246</p> <p>8.4 Synthetic Biology for Production of Lactate-Based Polymers 247</p> <p>8.4.1 Creation of Lactate-Polymerizing Enzyme (LPE) 247</p> <p>8.4.2 Biosynthesis of Lactate-Based Polymers 249</p> <p>8.4.3 Integrated Production Process of Lactate-Based Polymers from Renewable Feedstock 251</p> <p>8.4.4 Biosynthesized Lactate-Based Polymer Shows Superior Properties 253</p> <p>8.5 Outlook 254</p> <p>References 255</p> <p><b>9 Natural and Synthetic Biopolymers in Drug Delivery and Tissue Engineering </b><b>265<br /></b><i>John D. Schneible, Michael A. Daniele, and Stefano Menegatti</i></p> <p>9.1 Introduction 265</p> <p>9.2 Synthetic and Natural Substrates 267</p> <p>9.3 Applications of Natural and Synthetic Polypeptides 267</p> <p>9.3.1 Drug Delivery Vehicles 267</p> <p>9.3.2 Targeting Agents 273</p> <p>9.3.3 Cell-Permeating Peptides 274</p> <p>9.3.4 Peptides in Tissue Engineering and Regenerative Medicine 276</p> <p>9.4 Applications of Polysaccharides 280</p> <p>9.4.1 Drug Delivery 280</p> <p>9.4.2 Tissue Engineering and Regenerative Medicine 284</p> <p>9.5 Conclusions and Future Outlook 290</p> <p>References 290</p> <p><b>10 Biopolymers in Regenerative Medicine: Overview, Current Advances, and Future Trends </b><b>357<br /></b><i>Michael R. Behrens and Warren C. Ruder</i></p> <p>10.1 Introduction 357</p> <p>10.2 Biopolymer Scaffold Assembly 358</p> <p>10.2.1 Hydrogel Biopolymer Scaffolds 358</p> <p>10.2.2 Electrospinning of Biopolymer Scaffolds 360</p> <p>10.2.3 Three-Dimensional Printing of Biopolymer Scaffolds 362</p> <p>10.3 Organ System Specific Biopolymer Scaffolds 367</p> <p>10.3.1 Biopolymers for Musculoskeletal System Regeneration 368</p> <p>10.3.1.1 Biopolymers for Bone Regeneration 368</p> <p>10.3.1.2 Biopolymers for Cartilage Regeneration 370</p> <p>10.3.1.3 Biopolymers for Ligament and Tendon Regeneration 371</p> <p>10.3.2 Biopolymers for Cardiovascular System Regeneration 372</p> <p>10.3.2.1 Biopolymers for Vascular Regeneration 373</p> <p>10.3.2.2 Biopolymers for Cardiac Regeneration 374</p> <p>10.4 Summary and Outlook 376</p> <p>References 377</p> <p>Index 381</p>
Bernd Rehm received his MSc and PhD degrees (microbiology) from the Ruhr University Bochum, Germany, in 1991 and 1993, respectively. He continued as a postdoc at the Department of Microbiology and Immunology at the University of British Columbia, Canada. From 1996 to 2003, he was a research group leader at the Institute of Molecular Microbiology and Biotechnology at the University of Münster, Germany, where he also completed his habilitation. In 2003 he was appointed as Associate Professor and in 2005 promoted to Full Professor/Chair of Microbiology at Massey University in New Zealand. From 2013 to 2016 he was principal investigator of the Centre of Research Excellence (New Zealand) at the MacDiarmid Institute of Advanced Materials and Nanotechnology. He was recently appointed as Director of the Centre for Cell Factories and Biopolymer at Griffith University (Griffith Institute for Drug Discovery, Australia), and is the founder and chief technology officer of the biotechnology start-up company PolyBatics Ltd.<br> He is editor-in-chief and editor of 5 scientific journals as well as an editorial board member of 10 scientific journals and the sole editor of 5 books. He has authored over 200 scientific publications, and holds more than 30 patents. His R&D interests are in the microbial production of polymers and their applications. His recent studies focused on the use of engineered microorganisms to produce functionalized nano-/micro-structures for applications in diagnostics, enzyme immobilization, and antigen delivery.<br> <br> Dr. Fata Moradali received his MSc degree from Tehran University and his PhD degree in molecular microbiology and genetics from Massey University, New Zealand. Early years of his career were spend for investigating bioactive components from natural resources particularly fungi. Then, it was followed by spending several years in Prof. Bernd Rehm`s laboratory investigating molecular mechanism of alginate biosynthesis and signaling pathways in the model organism Pseudomonas aeruginosa. He then moved to the Department of Oral Biology, Florida University, USA, to join Dr. Mary Ellen Davey`s laboratory to continue cutting-edge research in the field of human oral biology and microbiota. Dr. Moradali has contributed to our understanding of bacterial physiology and pathogenesis and the molecular mechanism of alginate biosynthesis in P. aeruginosa as a model organism. His research has provided new insights into the molecular mechanism of alginate polymerization/modification and its activation by bacterial second messenger cyclic di-GMP. By employing genetic engineering in his research, he demonstrated the production of various alginates from P. aeruginosa for the production of tailor- made alginate. He has extensive expertise in microbial genetics and physiology with respect to pathogenesis as well as production of microbial compounds.

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