Literature DB >> 8514119

Determination of plasmid copy number and stability in Clostridium acetobutylicum ATCC 824.

S Y Lee1, L D Mermelstein, E T Papoutsakis.   

Abstract

The copy number and stability of several plasmid vectors in Clostridium acetobutylicum ATCC 824 were determined. The protocols were modified from the traditional ones to overcome the problems associated with unusual behavior of C. acetobutylicum cells on solid medium. The plasmid copy numbers of pSYL2, pFNK1, pFNK3, and pFNK5 in strain ATCC 824 were 14, 8, 6, and 6, respectively. pSYL2 and pFNK1 were segregationally stable, since the fractions of plasmid-carrying cells after 60 generations of growth without antibiotic (erythromycin) were 73% and 77%, respectively. Vector pFNK1 carrying fermentative genes was found to be rather unstable. The observed instability seemed to be due to the complex host-plasmid interactions by amplified expression of enzymes involved in the tightly regulated primary metabolism of C. acetobutylicum.

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Year:  1993        PMID: 8514119     DOI: 10.1111/j.1574-6968.1993.tb06122.x

Source DB:  PubMed          Journal:  FEMS Microbiol Lett        ISSN: 0378-1097            Impact factor:   2.742


  8 in total

1.  Control of butanol formation in Clostridium acetobutylicum by transcriptional activation.

Authors:  Kai Thormann; Lothar Feustel; Karin Lorenz; Stephan Nakotte; Peter Dürre
Journal:  J Bacteriol       Date:  2002-04       Impact factor: 3.490

2.  Characterization and development of two reporter gene systems for Clostridium acetobutylicum.

Authors:  Lothar Feustel; Stephan Nakotte; Peter Dürre
Journal:  Appl Environ Microbiol       Date:  2004-02       Impact factor: 4.792

3.  Expression of abrB310 and SinR, and effects of decreased abrB310 expression on the transition from acidogenesis to solventogenesis, in Clostridium acetobutylicum ATCC 824.

Authors:  Miles C Scotcher; Frederick B Rudolph; George N Bennett
Journal:  Appl Environ Microbiol       Date:  2005-04       Impact factor: 4.792

4.  A Strongly Fluorescing Anaerobic Reporter and Protein-Tagging System for Clostridium Organisms Based on the Fluorescence-Activating and Absorption-Shifting Tag Protein (FAST).

Authors:  Hannah E Streett; Katie M Kalis; Eleftherios T Papoutsakis
Journal:  Appl Environ Microbiol       Date:  2019-07-01       Impact factor: 4.792

5.  SpoIIE regulates sporulation but does not directly affect solventogenesis in Clostridium acetobutylicum ATCC 824.

Authors:  Miles C Scotcher; George N Bennett
Journal:  J Bacteriol       Date:  2005-03       Impact factor: 3.490

6.  Metabolic engineering of Escherichia coli for production of enantiomerically pure (R)-(--)-hydroxycarboxylic acids.

Authors:  Sang Yup Lee; Young Lee
Journal:  Appl Environ Microbiol       Date:  2003-06       Impact factor: 4.792

7.  Novel system for efficient isolation of Clostridium double-crossover allelic exchange mutants enabling markerless chromosomal gene deletions and DNA integration.

Authors:  Mohab A Al-Hinai; Alan G Fast; Eleftherios T Papoutsakis
Journal:  Appl Environ Microbiol       Date:  2012-09-14       Impact factor: 4.792

8.  Cas9 Nickase-Assisted RNA Repression Enables Stable and Efficient Manipulation of Essential Metabolic Genes in Clostridium cellulolyticum.

Authors:  Tao Xu; Yongchao Li; Zhili He; Joy D Van Nostrand; Jizhong Zhou
Journal:  Front Microbiol       Date:  2017-09-07       Impact factor: 5.640

  8 in total

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