New<i> Bacillus subtilis</i> vector, pSSβ, as genetic tool for site-specific integration and excision of cloned DNA, and prophage elimination
Author:
Affiliation:
1. Research Center of Micro-Nano Technology, Hosei University
2. Department of Frontier Bioscience, Hosei University
Publisher
Microbiology Research Foundation
Subject
Applied Microbiology and Biotechnology,Microbiology
Link
https://www.jstage.jst.go.jp/article/jgam/68/2/68_2021.10.004/_pdf
Reference29 articles.
1. Abe, K., Kawamura, Y., Iwamoto, K., Arai, K., Maruyama, Y., et al. (2014) Developmentally-regulated excision of the SPβ prophage reconstitutes a gene required for spore envelope maturation in Bacillus subtilis. PLoS Genet., 10, e1004636.
2. Abe, K., Takamatsu, T., and Sato, T. (2017) Mechanism of bacterial gene rearrangement: SprA-catalyzed precise DNA recombination and its directionality control by SprB ensure the gene rearrangement and stable expression of spsM during sporulation in Bacillus subtilis. Nucleic. Acids. Res., 45, 6669-6683.
3. Albertini, M. A. and Galizzi, A. (1999) The sequence of the trp operon of Bacillus subtilis 168 (trpC2). Microbiology, 145, 3319-3320.
4. Asadulghani, M., Ogura, Y., Ooka, T., Itoh, T., Sawaguchi, A., et al. (2009) The defective prophage pool of Escherichia coli O157: prophage-prophage interactions potentiate horizontal transfer of virulence determinants. PLoS Pathog, 5, e1000408.
5. Burkholder, P. R. and Giles, N. H., Jr. (1947) Induced biochemical mutations in Bacillus subtilis. Am. J. Bot., 34, 345-8.
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