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PMID: 3053647 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, Non-P.H.S. Research Support, U.S. Gov't, P.H.S.

Identification, cloning, and expression of bolA, an ftsZ-dependent morphogene of Escherichia coli.

Journal of bacteriology ·Vol. 170 ·No. 11 ·1988-11-00 ·Pages 5169-76

Aldea M, Hernández-Chico C, de la Campa AG, Kushner SR, Vicente M

Abstract

A newly found morphogene of Escherichia coli, bolA, mapping at min 10 of the genetic map, was cloned in a 7.2-kilobase BamHI fragment and identified by its ability to produce osmotically stable spherical cells when overexpressed. This gene codes for a polypeptide of 13 kilodaltons. Overexpression of bolA+ was achieved in low-copy-number vectors with operon fusions to the tet and lac promoters, indicating a clockwise direction of transcription. While no modification of any of the penicillin-binding proteins was observed, morphological effects due to overexpression of bolA+ were shown to be dependent on the presence of an active ftsZ gene product. Our results suggest the existence of a mechanism mediated by FtsZ for modifying the conformation of nascent murein in the early steps of septum formation.

MeSH Terms
Cell Division Cloning, Molecular Escherichia coli/cytology,genetics,growth & development Genes, Bacterial Genetic Linkage Genetic Vectors Morphogenesis Plasmids Promoter Regions, Genetic Restriction Mapping Transcription, Genetic Transduction, Genetic
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Aldea M
Department of Genetics, University of Georgia, Athens 30602.
Hernández-Chico C
de la Campa A G
Kushner S R
Vicente M
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Article Info
Journal
Journal of bacteriology
Abbr.
J Bacteriol
ISSN
0021-9193
Published
1988-11-00
Pages
5169-76
Language
English
Region
United States
NLM ID
2985120R
PMCID
PMC211586
Subset
IM
Grants
NIGMS NIH HHS · GM27997 · United States
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