In vivo expression of the Bacillus subtilis spoVE gene

Author:

Theeragool G1,Miyao A1,Yamada K1,Sato T1,Kobayashi Y1

Affiliation:

1. Faculty of Agriculture, Tokyo University of Agriculture and Technology, Fuchu, Japan.

Abstract

In vivo expression of the Bacillus subtilis spoVE gene was studied by S1 nuclease mapping and spoVE gene fusion analysis. Transcription of spoVE is induced at about the second hour of sporulation from two closely spaced promoters designated P1 and P2. Examination of the precise transcription initiation site by high-resolution primer extension mapping indicated that the nucleotide sequences of the -10 and -35 regions of both P1 and P2 were similar to those of promoters recognized by E sigma E. Moreover, S1 nuclease mapping and translational spoVE-lacZ fusion studies with various spo mutants suggest that the expression of spoVE P2 requires the spoIIG gene product, sigma E. The sporulation of a wild-type strain was inhibited severely in the presence of a multicopy plasmid, pKBVE, carrying the spoVE promoter, indicating the possible titration of a transcriptional regulatory element(s).

Publisher

American Society for Microbiology

Subject

Molecular Biology,Microbiology

Reference31 articles.

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4. Developmental and genetic regulation of Bacillus subtilis genes transcribed by cr 8 RNA polymerase;Gilman M. Z.;Cell,1983

5. A Bacillus subtilis morphogene cluster that includes spoVE is homologous to the mra region of Escherichia coli;Henriques A. O.;Biochimie,1992

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