Genomic analysis of Bacillus subtilis lytic bacteriophage ΦnIT1 capable of obstructing natto fermentation carrying genes for the capsule-lytic soluble enzymes poly-γ-glutamate hydrolase and levanase

Tatsuro Ozaki, Naoki Abe, Keitarou Kimura, Atsuto Suzuki, Jun Kaneko

研究成果: Article査読

12 被引用数 (Scopus)

抄録

Bacillus subtilis strains including the fermented soybean (natto) starter produce capsular polymers consisting of poly-γ-glutamate and levan. Capsular polymers may protect the cells from phage infection. However, bacteriophage ΦNIT1 carries a γ-PGA hydrolase gene (pghP) that help it to counteract the host cell's protection strategy. ΦNIT had a linear double stranded DNA genome of 155,631-bp with a terminal redundancy of 5,103-bp, containing a gene encoding an active levan hydrolase. These capsulelytic enzyme genes were located in the possible foreign gene cluster regions between central core and terminal redundant regions, and were expressed at the late phase of the phage lytic cycle. All tested natto origin Spounavirinae phages carried both genes for capsule degrading enzymes similar to ΦNIT1. A comparative genomic analysis revealed the diversity among ΦNIT1 and Bacillus phages carrying pghP-like and levan-hydrolase genes, and provides novel understanding on the acquisition mechanism of these enzymatic genes.

本文言語English
ページ(範囲)135-146
ページ数12
ジャーナルBioscience, Biotechnology and Biochemistry
81
1
DOI
出版ステータスPublished - 2017

ASJC Scopus subject areas

  • バイオテクノロジー
  • 分析化学
  • 生化学
  • 応用微生物学とバイオテクノロジー
  • 分子生物学
  • 有機化学

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