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PMID: 8825779 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

Polynucleotide phosphorylase is necessary for competence development in Bacillus subtilis.

Molecular microbiology ·Vol. 19 ·No. 2 ·1996-01-00 ·Pages 343-56

Luttinger A, Hahn J, Dubnau D

Abstract

comR (pnpA) is a newly identified gene in Bacillus subtilis that is necessary for the expression of late competence genes. Transformability of a comR (pnpA) mutant is 1-5% of that seen in comR+ strains. Cloning and sequencing identified ComR as polynucleotide phosphorylase (PNPase). The PNPase amino acid sequence has 50% identity and 67% similarity with the Escherichia coli enzyme. Enzymatic assays show that this is the only PNPase activity in B. subtilis. comR (pnpA) is necessary for comG-lacZ and comK-lacZ expression, but this requirement is bypassed by a mecA disruption. In B. subtilis, the loss of PNPase has little effect on expression from a fusion of the srfA promoter directly to lacZ, but is necessary for normal expression from certain srfA-lacZ fusions that include portions of the normal srfA transcript. When a srfA-lacZ translational fusion is tested in isogenic pnpA+ and pnpA derivatives of E. coli, lower expression is seen in the pnpA mutant. Since expression from lacZ fusions to comA, sinR, and mecA appeared similar in the B. subtilis pnpA and pnpA+ strains, the loss of PNPase does not have a strong general effect on gene expression. These results suggest that PNPase may be necessary for modification of the srfA transcript in order to activate translation or stabilize the transcript, and that this may be necessary for competence development. This is the first evidence of post-transcriptional effects on the development of competence in B. subtilis.

MeSH Terms
Amino Acid Sequence Bacillus subtilis/enzymology,genetics Bacterial Proteins/metabolism Base Sequence Chromosome Mapping Cloning, Molecular Cold Temperature DNA, Bacterial/genetics,metabolism Epistasis, Genetic Gene Expression Regulation, Bacterial/genetics Lac Operon/genetics Lipopeptides Molecular Sequence Data Peptide Synthases/genetics Peptides, Cyclic Polyribonucleotide Nucleotidyltransferase/metabolism Sequence Homology, Amino Acid Transformation, Bacterial
Chemicals
Bacterial Proteins DNA, Bacterial Lipopeptides Peptides, Cyclic surfactin peptide Polyribonucleotide Nucleotidyltransferase Peptide Synthases surfactin synthetase
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Luttinger A
Public Health Research Institute, New York, New York 10016, USA.
Hahn J
Dubnau D
Article Info
Journal
Molecular microbiology
Abbr.
Mol Microbiol
ISSN
0950-382X
Published
1996-01-00
Pages
343-56
Language
English
Region
England
NLM ID
8712028
Subset
IM
Grants
NIAID NIH HHS · AI10311 · United States
Databases
GENBANK
U29668, Z80835
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