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

Research output: Contribution to journalArticlepeer-review

12 Citations (Scopus)

Abstract

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.

Original languageEnglish
Pages (from-to)135-146
Number of pages12
JournalBioscience, Biotechnology and Biochemistry
Volume81
Issue number1
DOIs
Publication statusPublished - 2017

Keywords

  • Bacillus subtilis phage
  • Genome
  • Levanase
  • Transcription
  • γ-PGA hydrolase

ASJC Scopus subject areas

  • Biotechnology
  • Analytical Chemistry
  • Biochemistry
  • Applied Microbiology and Biotechnology
  • Molecular Biology
  • Organic Chemistry

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