Advances in applied microbiology. Vol. 118 /
Advances in Applied Microbiology, Volume 118 continues the comprehensive reach of this widely read and authoritative review source in microbiology.Users will find invaluable references and information on a variety of areas relating to the topics of microbiology.- Contains contributions from leading...
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| Other Authors: | , |
| Format: | eBook |
| Language: | English |
| Published: |
Cambridge, MA :
Academic Press,
[2022]
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| Edition: | First edition. |
| Series: | Advances in applied microbiology.
v. 118. |
| Subjects: | |
| Online Access: | Connect to the full text of this electronic book |
Table of Contents:
- Chapter 1: CRISPR/Cas genome editing systems in thermophiles: Current status, associated challenges, and future perspectives
- 1. Introduction
- 2. Genetic engineering in thermophilic organisms
- 2.1. Selection marker in thermophiles
- 2.2. Strategies for the transformation of thermophiles
- 2.3. Shuttle vectors for thermophiles
- 2.4. Advance of gene deletion and integration system in thermophiles
- 3. CRISPR tool kit in thermopholes
- 3.1. Development and application of endogenous type I and III CRISPR/Cas based technologies in thermophiles
- 3.2. Development and application of type II CRISPR/Cas9 based technologies in thermophiles
- 3.2.1. SpCas9 mediated genome editing in moderate thermophiles
- 3.2.2. Characterization of thermostable Cas9
- 3.2.3. ThermoCas9 mediated genome editing in B. smithii
- 3.2.4. GeoCas9 mediated genome editing in C. thermocellum
- 3.2.5. GeoCas9 mediated genome editing in T. ethanolicus
- 3.2.6. CaldoCas9 mediated genome editing in T. thermophilus
- 3.3. Development and application of CRISPR interference technologies in thermophiles
- 4. Associated challenges and future perspectives
- 4.1. A challenge in the introduction of DNA into thermophilic host cells
- 4.2. A challenge in a controllable expression of thermostable Cas9 and sgRNA
- 4.3. A challenge in the homology directed repair
- 4.4. Construction of thermophilic microbial cell factory
- 5. Conclusion
- Acknowledgments
- References
- Chapter 2: Microbial mercury transformations: Molecules, functions and organisms
- 1. Introduction
- 2. Mercury methylation
- 2.1. Hg methylation mechanisms
- 2.2. Geochemical factors influencing Hg methylation
- 2.2.1. SO4
- 2.2.2. Natural organic matter
- 2.2.3. Iron (Fe)
- 2.2.4. Inorganic nutrients
- 2.3. Previously-recognized and newly-discovered Hg methylating microbes
- 2.3.1. Mercury methylating sulfate reducing bacteria (SRB)
- 2.3.2. Mercury methylating iron reducing bacteria (FeRB)
- 2.3.3. Mercury methylating methanogens
- 2.3.4. Mercury methylating syntrophs
- 2.3.5. Other novel species of mercury methylating prokaryotes
- 2.4. Evolutionary and environmental implication of putative hgcAB genes
- 3. Demethylation
- 3.1. Reductive and oxidative biotic demethylation processes
- 3.2. Reductive demethylation, or mer-dependent degradation to Hg(0) and CH4
- 3.2.1. Mechanism of MerB activity
- 3.2.2. Diversity, evolution, and distribution of MerB and microbes that reductively demethylate MeHg
- 3.3. Oxidative demethylation
- 3.4. Methanotrophic demethylation
- 4. Redox transformations of inorganic mercury
- 4.1. Inorganic mercury reduction
- 4.2. Inorganic Hg oxidation
- Acknowledgments
- References
- Chapter 3: Microbial community signatures for estimation of postmortem time intervals
- 1. Introduction
- 2. Signature microbes and their distribution in the human body
- 2.1. Skin microbiome
- 2.2. Oral microbiome
- 2.3. Microbiome of respiratory tract
- 2.4. Urinary system´s microbiome
- 2.5. Microbiome of the human genital system
- 2.6. Digestive system microbiome
- 2.7. Other internal organs
- 3. Molecular insight of change in human microenvironment postmortem
- 4. Stages of decomposition
- 5. Changes in signature microflora postmortem
- 6. Techniques to study postmortem signature microflora
- 6.1. Extraction of DNA from challenging samples
- 6.2. Availability of group-specific primers
- 6.3. Metagenomics
- 6.4. Whole-genome sequencing
- 6.5. Modeling techniques
- 7. Conclusion
- References.