Isolation and Characterization of Sporulation-Initiation Mutation in theBacillus subtilisprfBGene
Author(s) -
Kei Asai,
Takashi Inaoka,
Hideaki Nanamiya,
Yoshito Sadaie,
Kozo Ochi,
Fujio Kawamura
Publication year - 2007
Publication title -
bioscience biotechnology and biochemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.509
H-Index - 116
eISSN - 1347-6947
pISSN - 0916-8451
DOI - 10.1271/bbb.60445
Subject(s) - bacillus subtilis , mutant , rpob , spore , biology , gene , genetics , mutation , ribosome , microbiology and biotechnology , rna , bacteria , 16s ribosomal rna
A Bacillus subtilis prfB45 mutant grew at 42 degrees C, but its sporulation was severely defective at 37 degrees C. Sporulation-specific induction of kinA, spo0A, and spo0H genes was inhibited in the mutant. The effects of temperature up-shift and down-shift on sporulation of the prfB45 mutant was observed at an early stage of sporulation. UGA readthrough frequency at non-permissive temperatures for sporulation was higher in the mutant than in the wild-type strain. Temperature-sensitive sporulation of the prfB45 mutant was suppressed by mutations in rpsL coding for S12 of ribosomes, required for accurate termination of translation. Additionally, spontaneous second-site mutations that suppressed the sporulation phenotype of the prfB45 strain were found in the rpoB gene. These results suggest that accurate termination of translation is required for proper initiation of sporulation.
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