New and Future Developments in Microbial Biotechnology and Bioengineering :Microbial Genes Biochemistry and Applications

Publication subTitle :Microbial Genes Biochemistry and Applications

Author: Singh   H. B;Gupta   Vijai G.;Jogaiah   Sudisha  

Publisher: Elsevier Science‎

Publication year: 2018

E-ISBN: 9780444635105

P-ISBN(Paperback): 9780444635037

Subject: Q Biological Sciences;Q3 Genetics;Q93 Microbiology

Keyword: 微生物学,遗传学,生物科学

Language: ENG

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Description

New and Future Developments in Microbial Biotechnology and Bioengineering: Microbial Genes Biochemistry and Applications consolidates the most widely used genetic methods available, bringing together the fields of biochemistry, biotechnology and microbiology. Chapters give clear-and-concise direction on both standard and applied microbial genetic improvements, presenting undergraduates, post-graduates and researchers with the latest developments in microbial gene technology. In addition, the book describes the background and usefulness of each experiment in question. All chapters covered in the book are derived from current, peer reviewed literature accepted by the international scientific community.

  • Compiles the latest developments in the area of microbial gene systems
  • Includes information on almost all areas of microbial gene technology
  • Relates microbial engineering and its direct application to the production of many useful compounds, i.e., pharmaceuticals
  • Written by an international team of authors

Chapter

1.3.2.2 Enzymes Involved in Polychlorinated Biphenyls Degradation

1.3.2.3 Polychlorinated Biphenyls Catabolic Genes

1.3.3 Biodiversity of Biphenyl Compounds Degrading Microbes

1.4 New Developments on Microbes Proficient in Enhanced Biodegradation

1.5 Conclusion and Future Prospects

Acknowledgment

References

Further Reading

2 Genetics and Molecular Biology of Genes Encoding Cephalosporin Biosynthesis in Microbes

2.1 Introduction

2.2 Cephalosporin: The First Stable β-Lactam

2.2.1 Genetics of Cephalosporin Biosynthesis

2.2.2 Cephalosporin Biosynthesis: Organization and Expression Pattern

2.2.3 Molecular Biology of A. chrysogenum

2.3 Advantages of Cephalosporin

2.4 Cephalosporin: Classification and Generations

2.4.1 Cephalosporin: First Generation

2.4.2 Cephalosporin: Second Generation

2.4.3 Cephalosporin: Third Generation

2.4.4 Cephalosporin: Fourth Generation

2.4.5 Cephalosporin: Fifth Generation

2.5 Cephalosporin: Mechanism of Action

2.6 Resistance to Cephalosporin

2.7 Summary

References

3 Disruption of Protease Genes in Microbes for Production of Heterologous Proteins

3.1 Introduction

3.2 Molecular and Biotechnological Aspects of Microbial Proteases

3.3 Biodiversity of Heterologous Proteins Producing Microbes

3.4 Problems Associated With Proteases and Approaches to Tackle These Problems

3.4.1 Disruption of Interfering Protease Genes

3.4.2 Classical Mutagenesis

3.4.3 Optimizing the Media Composition

3.5 Microbes as Cell Factory for Foreign Proteins

3.5.1 Enzyme Industry

3.5.2 Biopharmaceuticals

3.5.2.1 Escherichia coli

3.5.2.2 Bacilli

3.5.2.3 Lactococcus lactis

3.5.2.4 Streptomyces

3.5.2.5 Saccharomyces cerevisiae

3.5.2.6 Pichia pastoris

3.5.2.7 Filamentous fungi

3.6 Strategies for Improving Heterologous Protein Production

3.6.1 Basic Requirements for Expression of Heterologous Proteins

3.6.1.1 Promoters

3.6.1.2 Vectors

3.6.1.3 Increase in Copy Number

3.6.1.4 Site-Specific Recombination

3.6.1.5 Aspects of Secretory Expression

3.6.2 Host Strain Development

3.6.2.1 Auxotrophic Strains

3.6.2.2 Glyco-Engineered Strains

3.6.2.3 Protease-Deficient Strains

3.6.3 Molecular Strategies for Heterologous Protein Production

3.6.3.1 Gene-Fusions Strategies

3.6.3.2 Overproduction of Foldases and Chaperones

3.7 Conclusion and Future Perspectives

Acknowledgments

References

Further Reading

4 Function Profiling of Microbial Community

4.1 Introduction

4.2 Method to Study Functional Analysis

4.2.1 Metagenomic Analysis

4.2.1.1 Predicted Functional Analysis

4.2.1.2 Function-Based Analysis

Phenotypic Detection of the Novel Gene

Heterologous Complementation of Host Strains or Mutant

Substrate Induced Gene Expression

4.2.2 Metatranscriptomic Analysis

4.2.3 Metaproteomics Analysis

4.3 Conclusion

References

Further Reading

5 Enhanced Resistance to Fungal Pathogens Through Selective Utilization of Useful Microbial Genes

5.1 Introduction

References

6 Differential Expression of the Microbial β-1,4-Xylanase, and β-1,4-Endoglucanase Genes

6.1 Introduction

6.1.1 β-1,4-Xylanases

6.1.2 Xylanase Family

6.1.3 β-1,4-Endoglucanase

6.1.4 β-1,4-Endoglucanase Family

6.2 Mechanism of β-1,4-Xylanase and β-1,4-Endoglucanase Action

6.2.1 Genes Encoding β-1,4-Xylanases

6.2.2 Genes Encoding β-1,4-Endoglucanase

6.3 Expression Studies of β-1,4-Xylanases and Their Properties

6.3.1 Expression and Characterization of β-1,4-Endoglucanases

6.3.2 Regulation of β-1,4-Xylanase and β-1,4-Endoglucanase Gene Expression

6.4 Conclusions

References

7 Profile of Secondary Metabolite Gene Cluster in Microbe

7.1 Introduction

7.2 Antibiotic Resistance Engineering

7.3 Entire Gene Clusters’ Heterogeneous Expression

7.4 Genome Mining of Secondary Metabolite Producers on a Platform

7.5 Microbial Communication: An Inducer of Silent Secondary Metabolite Gene Clusters

7.6 The Interaction of Fungi With Bacteria

7.7 Rifampin Resistance (rpoB) Mutations in Actinomycetes for Biosynthetic Gene Clusters

7.8 Conclusions

References

8 Production of Recombinant Microbial Thermostable Lipases

8.1 Introduction

8.2 Characteristics of Thermostable Lipases

8.3 Sources and Biotechnological Application of Thermostable Lipases

8.4 Detergent Industries

8.4.1 Food Industries

8.4.2 Medical and Pharmaceutical Applications

8.4.3 Pulp and Paper Industry

8.4.4 Organic Synthesis and Oleochemical Industry

8.4.5 Mitigation of Ecological Pollution

8.5 Expression of Thermostable Lipases

8.5.1 Prokaryotic Systems for the Expression of Thermostable Lipases

8.5.2 Strategies for the Expression of Thermostable Lipases in Prokaryotic Systems

8.5.3 Eukaryotic Systems for the Expression of Thermostable Lipases

8.6 Conclusions: Current Challenges and Future Perspectives

References

9 Isolation of Cellulase Genes From Thermophilies: A Novel Approach Toward New Gene Discovery

9.1 Introduction

9.2 Discoveries of Cellulase Genes and its Expression

9.3 Approaches Toward Isolation of Cellulase Genes

9.3.1 Conventional Approach

9.3.2 Genomic DNA Library

9.3.2.1 Advatntages and Disadvantages

9.3.3 Metagenomic DNA Library

9.3.3.1 Advantages and Disadvantages

9.3.3.2 Advantages and Disadvantages

9.3.4 Bioinformatics Approach

9.3.4.1 Advantages and Disadvantages

9.4 Conclusion

Acknowledgment

References

Further Reading

10 Microbial Genes Involved in Interaction With Plants

10.1 Introduction

10.1.1 Biological Nitrogen Fixation (Positive Interaction)

10.1.1.1 Mechanism of Nitrogen Fixation and nif Genes

10.1.1.2 Working of Enzyme Nitrogenase

10.1.1.3 Other Genes Involved in Nodulation and Nitrogen Fixation

10.1.2 Microbial Interaction With Plants and Pathogenesis (Negative Interaction)

10.1.2.1 Horizontal Transmission of T-DNA Genes

10.1.2.2 Mechanism of Bacterial Pathogenesis: A Model for Plant–Bacterium Interactions and Coevolution Based on Hrp Deliver...

10.1.2.3 Oncogenes

10.2 Conclusions

References

Further Reading

11 Virulence Factors and Their Associated Genes in Microbes

11.1 Introduction

11.2 Virulence Factors and Genes in Fungal Pathogens

11.2.1 Role of Genes in Degradation of Host Structure and Metabolism

11.2.1.1 Cell Wall-Degrading Enzymes (CWDEs)

11.2.1.2 Toxins

11.2.1.3 Lipids as Fungal Virulence Factors

11.2.2 Signaling

11.2.2.1 Heterotrimeric GTP-Binding Proteins (G-Proteins)

11.2.2.2 cAMP Signaling Pathways

11.2.2.3 Mitogen-Activated Protein Kinases (MAPKs)

11.2.3 Genes Responsible for Virulence

11.3 Virulence Factors Genes in Bacteria

11.3.1 Virulence Factors and Genes in Bacterial Pathogens

11.3.1.1 Extracellular Polysaccharide (EPS)

11.3.1.2 Motility and Virulence

11.3.1.3 Quorum Sensing (QS)

11.3.1.4 Cell Wall Degrading Enzymes (CWDEs)

11.3.1.5 Toxins

11.3.1.6 Secretion System

Type I Secretion System (T1SS)

Type II Secretion System (T2SS)

Type III Secretion System

Type IV Secretion System (T4SS)

11.3.2 Regulation of Virulence Factors

11.3.2.1 Sigma Factors

11.3.2.2 Two-Component Systems

11.4 Virulence Factor Genes in Viruses

11.5 Conclusion

References

Further Reading

12 Modulation of Gene Expression by Microsatellites in Microbes

12.1 Introduction

12.2 Classification of Microsatellites

12.3 Origin of Microsatellites

12.4 Distribution of Microsatellites

12.5 Microsatellite Instability (MSI) Phenomenon

12.6 Functional Significance of Microsatellites

12.7 Microsatellites in Gene Expression

12.8 Microsatellites in Evolutionary Studies

12.9 Microsatellites in Bacterial Pathogenesis

12.10 Role of Microsatellites in Adaptation

12.11 Conclusion

References

Further Reading

13 Polyketide and Its Derivatives

13.1 Introduction

13.2 Polyketide Synthesis

13.2.1 Type 1 PKSs

13.2.2 Type 2 PKSs

13.2.3 Type 3 PKSs

13.3 Conclusions

References

Further Reading

14 Synthetic Biology Strategy for Microbial Cellulases: An Overview

14.1 Introduction

14.2 Significance of Cellulases in Biofuels Production

14.3 Fungal Microorganisms for Cellulase Production

14.4 Bacterial Microorganisms for Cellulase Production

14.5 Role of Synthetic Biology to Improve Cellulase Systems

14.5.1 Expression Systems in Fungi to Produce Cellulase Enzymes

14.5.1.1 Role of RNA Interference for Fungal Cellulase Production

14.5.2 Yeast Expression Systems for Cellulase Production

14.5.3 Expression Systems in Bacteria for Cellulase Production Analysis

14.6 Conclusions

Acknowledgment

References

Index

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