Determination and characterization of IS4Bsu1-insertion loci and identification of a new insertion sequence element of the IS256 family in a natto starter

被引:10
作者
Kimura, Keitarou [1 ]
Itoh, Yoshifumi [1 ]
机构
[1] Natl Food Res Inst, Div Appl Microbiol, Tsukuba, Ibaraki 3058642, Japan
基金
日本学术振兴会;
关键词
soybean fermentation; poly-gamma-glutamate production; integrative and conjugative element; polyketide synthesis; gene transfer;
D O I
10.1271/bbb.70223
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The insertion sequence IS4Bsu1 frequently causes Bacillus subtilis starters for the production of Japanese fermented soybean pasts (natto) to lose the ability to produce poly-gamma-glutamate, the viscous material characteristic of natto. Bacillus subtilis NAFM5, a derivative of a natto starter, has six IS4Bsu1 copies on its chromosome. In this study, we determined all six insertion loci of the insertion sequence (IS). One was located in the coding region of yktD, a putative gene involved in polyketide synthesis. Four were located in non-coding regions between iolR and iolA, between tuaA and lytC, between rapI and orf1 (a potential gene of unknown function), and between ynaE and orf3 (a putative gene similar to thiF), and one resided in an intergenic region between divergent possible orf4 and orf5 genes of unknown function. Here we describe the structural features of these loci and discuss the effects of the IS4Bsu1 insertions on the functions of the target gene and the expression of the downstream genes. In addition, we found that strain NAFM5 and commercial natto starters possess eight to 10 loci of another IS of the IS256 family (designated IS256Bsu1) on their chromosomes. IS256Bus1 appeared active in transposition, potentially causing phenotypic alterations in natto starters like those induced by IS4Bsu1.
引用
收藏
页码:2458 / 2464
页数:7
相关论文
共 37 条
[1]  
[Anonymous], 1989, Molecular Cloning
[2]   Regulation of a Bacillus subtilis mobile genetic element by intercellular signaling and the global DNA damage response [J].
Auchtung, JM ;
Lee, CA ;
Monson, RE ;
Lehman, AP ;
Grossman, AD .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2005, 102 (35) :12554-12559
[3]   Teichoic acid is an essential polymer in Bacillus subtilis that is functionally distinct from teichuronic acid [J].
Bhavsar, AP ;
Erdman, LK ;
Schertzer, JW ;
Brown, ED .
JOURNAL OF BACTERIOLOGY, 2004, 186 (23) :7865-7873
[4]   Synergistic regulation of competence development in Bacillus subtilis by two Rap-Phr systems [J].
Bongiorni, C ;
Ishikawa, S ;
Stephenson, S ;
Ogasawara, N ;
Perego, M .
JOURNAL OF BACTERIOLOGY, 2005, 187 (13) :4353-4361
[5]   TPR-mediated interaction of RapC with ComA inhibits response regulator-DNA binding for competence development in Bacillus subtilis [J].
Core, L ;
Perego, M .
MOLECULAR MICROBIOLOGY, 2003, 49 (06) :1509-1522
[6]   NUCLEOTIDE-SEQUENCES AND HETEROLOGOUS EXPRESSION OF TCMG AND TCMP, BIOSYNTHETIC GENES FOR TETRACENOMYCIN-C IN STREPTOMYCES-GLAUCESCENS [J].
DECKER, H ;
MOTAMEDI, H ;
HUTCHINSON, CR .
JOURNAL OF BACTERIOLOGY, 1993, 175 (12) :3876-3886
[7]   DNA uptake in bacteria [J].
Dubnau, D .
ANNUAL REVIEW OF MICROBIOLOGY, 1999, 53 :217-244
[8]   Bacillus subtilis RghR (YvaN) represses rapG and rapH, which encode inhibitors of expression of the srfA operon [J].
Hayashi, K ;
Kensuke, T ;
Kobayashi, K ;
Ogasawara, N ;
Ogura, M .
MOLECULAR MICROBIOLOGY, 2006, 59 (06) :1714-1729
[9]   Genetic analysis of the biosynthesis of non-ribosomal peptide- and polyketide-like antibiotics, iron uptake and biofilm formation by Bacillus subtilis A1/3 [J].
Hofemeister, J ;
Conrad, B ;
Adler, B ;
Hofemeister, B ;
Feesche, J ;
Kucheryava, N ;
Steinborn, G ;
Franke, P ;
Grammel, N ;
Zwintscher, A ;
Leenders, F ;
Hitzeroth, G ;
Vater, J .
MOLECULAR GENETICS AND GENOMICS, 2004, 272 (04) :363-378
[10]  
Hulett F. M., 2002, BACILLUS SUBTILIS IT, P193, DOI DOI 10.1128/9781555817992.CH15