Literature DB >> 35583738

Genome Editing Methods for Bacillus subtilis.

Katherine J Wozniak1, Lyle A Simmons2.   

Abstract

Bacillus subtilis is a widely studied Gram-positive bacterium that serves as an important model for understanding processes critical for several areas of biology including biotechnology and human health. B. subtilis has several advantages as a model organism: it is easily grown under laboratory conditions, it has a rapid doubling time, it is relatively inexpensive to maintain, and it is nonpathogenic. Over the last 50 years, advancements in genetic engineering have continued to make B. subtilis a genetic workhorse in scientific discovery. In this chapter, we describe methods for traditional gene disruptions, use of gene deletion libraries from the Bacillus Genetic Stock Center, allelic exchange, CRISPRi, and CRISPR/Cas9. Additionally, we provide general materials and equipment needed, strengths and limitations, time considerations, and troubleshooting notes to perform each method. Use of the methods outlined in this chapter will allow researchers to create gene insertions, deletions, substitutions, and RNA interference strains through a variety of methods custom to each application.
© 2022. Springer Science+Business Media, LLC, part of Springer Nature.

Entities:  

Keywords:  Bacillus subtilis; Genetic manipulation; Gram-positive;  CRISPR/Cas9;  Genetic engineering

Mesh:

Substances:

Year:  2022        PMID: 35583738      PMCID: PMC9519194          DOI: 10.1007/978-1-0716-2233-9_11

Source DB:  PubMed          Journal:  Methods Mol Biol        ISSN: 1064-3745


  23 in total

1.  The Bacillus subtilis competence transcription factor, ComK, overrides LexA-imposed transcriptional inhibition without physically displacing LexA.

Authors:  L W Hamoen; B Haijema; J J Bijlsma; G Venema; C M Lovett
Journal:  J Biol Chem       Date:  2001-09-12       Impact factor: 5.157

Review 2.  Internalizing DNA.

Authors:  D Dubnau; R Provvedi
Journal:  Res Microbiol       Date:  2000 Jul-Aug       Impact factor: 3.992

3.  Development of a new integration site within the Bacillus subtilis chromosome and construction of compatible expression cassettes.

Authors:  B Härtl; W Wehrl; T Wiegert; G Homuth; W Schumann
Journal:  J Bacteriol       Date:  2001-04       Impact factor: 3.490

4.  MinJ (YvjD) is a topological determinant of cell division in Bacillus subtilis.

Authors:  Joyce E Patrick; Daniel B Kearns
Journal:  Mol Microbiol       Date:  2008-10-02       Impact factor: 3.501

5.  MutS2 Promotes Homologous Recombination in Bacillus subtilis.

Authors:  Peter E Burby; Lyle A Simmons
Journal:  J Bacteriol       Date:  2016-12-28       Impact factor: 3.490

6.  Plasmid-encoded ComI inhibits competence in the ancestral 3610 strain of Bacillus subtilis.

Authors:  Melissa A Konkol; Kris M Blair; Daniel B Kearns
Journal:  J Bacteriol       Date:  2013-07-08       Impact factor: 3.490

7.  Gene position in a long operon governs motility development in Bacillus subtilis.

Authors:  Loralyn M Cozy; Daniel B Kearns
Journal:  Mol Microbiol       Date:  2010-03-10       Impact factor: 3.501

8.  Cre/lox system and PCR-based genome engineering in Bacillus subtilis.

Authors:  Xin Yan; Hao-Jie Yu; Qing Hong; Shun-Peng Li
Journal:  Appl Environ Microbiol       Date:  2008-07-18       Impact factor: 4.792

9.  Genetic recombination in Bacillus subtilis: a division of labor between two single-strand DNA-binding proteins.

Authors:  Tribhuwan Yadav; Begoña Carrasco; Angela R Myers; Nicholas P George; James L Keck; Juan C Alonso
Journal:  Nucleic Acids Res       Date:  2012-02-28       Impact factor: 16.971

10.  An efficient one-step site-directed deletion, insertion, single and multiple-site plasmid mutagenesis protocol.

Authors:  Huanting Liu; James H Naismith
Journal:  BMC Biotechnol       Date:  2008-12-04       Impact factor: 2.563

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.