Literature DB >> 10762236

A new IS4 family insertion sequence, IS4Bsu1, responsible for genetic instability of poly-gamma-glutamic acid production in Bacillus subtilis.

T Nagai1, L S Tran, Y Inatsu, Y Itoh.   

Abstract

Certain Bacillus subtilis strains, such as B. subtilis (natto) starter strains for the manufacture of natto (fermented soybeans), produce capsular poly-gamma-glutamate (gammaPGA). In B. subtilis (natto), gammaPGA synthesis is controlled by the ComP-ComA two-component regulatory system and thereby induced at the beginning of the stationary growth phase. We have found a new insertion sequence (IS), designated IS4Bsu1, in the comP gene of a spontaneous gammaPGA-negative mutant of B. subtilis (natto) NAF4. IS4Bsu1 (1,406 bp), the first IS discovered in B. subtilis, encodes a putative transposase (Tpase) with a predicted M(r) of 34,895 (374 residues) which displays similarity to the Tpases of IS4 family members. Southern blot analyses have identified 6 to 11 copies of IS4Bsu1, among which 6 copies were at the same loci, in the chromosomes of B. subtilis (natto) strains, including NAF4, three commercial starters, and another three gammaPGA-producing B. subtilis (natto) strains. All of the eight spontaneous gammaPGA(-) mutants, which were derived from five independent NAF4 cultures, had a new additional IS4Bsu1 copy in comP at six different positions within 600 bp of the 5'-terminal region. The target sites of IS4Bsu1 were determined to be AT-rich 9-bp sequences by sequencing the flanking regions of IS4Bsu1 in mutant comP genes. These results indicate that IS4Bsu1 transposes by the replicative mechanism, in contrast to other IS4 members that use the conservative mechanism, and that most, if not all, of spontaneous gammaPGA(-) mutants appear to have resulted from the insertion of IS4Bsu1 exclusively into comP. The presence of insertion hot spots in comP, which is essential for gammaPGA synthesis, as well as high transposition activity, would account for the high frequency of spontaneous gammaPGA(-) mutation by IS4Bsu1 in B. subtilis (natto).

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Year:  2000        PMID: 10762236      PMCID: PMC111298          DOI: 10.1128/JB.182.9.2387-2392.2000

Source DB:  PubMed          Journal:  J Bacteriol        ISSN: 0021-9193            Impact factor:   3.490


  42 in total

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Authors:  J P Mueller; G Bukusoglu; A L Sonenshein
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2.  Tn10 insertion specificity is strongly dependent upon sequences immediately adjacent to the target-site consensus sequence.

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Authors:  Y Kasahara; S Nakai; N Ogasawara
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4.  Novel insertion sequence IS1380 from Acetobacter pasteurianus is involved in loss of ethanol-oxidizing ability.

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Journal:  J Bacteriol       Date:  1991-11       Impact factor: 3.490

5.  IS231A transposition: conservative versus replicative pathway.

Authors:  C Léonard; J Mahillon
Journal:  Res Microbiol       Date:  1998-09       Impact factor: 3.992

6.  The complete genome sequence of Escherichia coli K-12.

Authors:  F R Blattner; G Plunkett; C A Bloch; N T Perna; V Burland; M Riley; J Collado-Vides; J D Glasner; C K Rode; G F Mayhew; J Gregor; N W Davis; H A Kirkpatrick; M A Goeden; D J Rose; B Mau; Y Shao
Journal:  Science       Date:  1997-09-05       Impact factor: 47.728

Review 7.  Target site selection in transposition.

Authors:  N L Craig
Journal:  Annu Rev Biochem       Date:  1997       Impact factor: 23.643

8.  Biochemical and genetic characterization of a competence pheromone from B. subtilis.

Authors:  R Magnuson; J Solomon; A D Grossman
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9.  IS231A insertion specificity: consensus sequence and DNA bending at the target site.

Authors:  B Hallet; R Rezsöhazy; J Mahillon; J Delcour
Journal:  Mol Microbiol       Date:  1994-10       Impact factor: 3.501

10.  An Acetobacter xylinum insertion sequence element associated with inactivation of cellulose production.

Authors:  D H Coucheron
Journal:  J Bacteriol       Date:  1991-09       Impact factor: 3.490

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  12 in total

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Authors:  H Takami; C G Han; Y Takaki; E Ohtsubo
Journal:  J Bacteriol       Date:  2001-07       Impact factor: 3.490

2.  The presence of the transposable element ISBsu2 from a cryptic plasmid in chromosomes of some Bacillus subtilis strains.

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3.  ISAba825, a functional insertion sequence modulating genomic plasticity and bla(OXA-58) expression in Acinetobacter baumannii.

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4.  Functional analysis of insertion sequence ISAba1, responsible for genomic plasticity of Acinetobacter baumannii.

Authors:  Pauline D Mugnier; Laurent Poirel; Patrice Nordmann
Journal:  J Bacteriol       Date:  2009-01-09       Impact factor: 3.490

5.  Phylogenetic analysis of Bacillus subtilis strains applicable to natto (fermented soybean) production.

Authors:  Yuji Kubo; Alejandro P Rooney; Yoshiki Tsukakoshi; Rikio Nakagawa; Hiromasa Hasegawa; Keitarou Kimura
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6.  Facilitation of direct conditional knockout of essential genes in Bacillus licheniformis DSM13 by comparative genetic analysis and manipulation of genetic competence.

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7.  Acinetobacter insertion sequence ISAba11 belongs to a novel family that encodes transposases with a signature HHEK motif.

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8.  Whole genome assembly of a natto production strain Bacillus subtilis natto from very short read data.

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9.  Comparative analysis of physical maps of four Bacillus subtilis (natto) genomes.

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10.  Social interactions and distribution of Bacillus subtilis pherotypes at microscale.

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Journal:  J Bacteriol       Date:  2008-12-29       Impact factor: 3.490

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