» Articles » PMID: 3038839

Phosphate Regulation of Gene Expression in Vibrio Parahaemolyticus

Overview
Journal J Bacteriol
Specialty Microbiology
Date 1987 Aug 1
PMID 3038839
Citations 29
Authors
Affiliations
Soon will be listed here.
Abstract

The synthesis of a major outer membrane protein, OmpP, in Vibrio parahaemolyticus was induced by growth in media deficient in phosphate. The gene, ompP, encoding this protein was cloned. Synthesis of OmpP in Escherichia coli was regulated by the availability of phosphate, and this control required the function of pho regulatory genes of E. coli. Analysis of gene fusion strains constructed by mutagenesis with transposon mini-Mulux revealed that ompP was transcriptionally regulated in V. parahaemolyticus. Impaired growth of a strain with an ompP defect was observed in media which contained large linear polyphosphates as the phosphate source. This and other evidence suggested that OmpP functions as a porin channel for the entry of phosphate into the cell. A number of other proteins or activities were induced by phosphate limitation including hemolysin, phospholipase C, and phosphatase activities. A regulatory locus controlling expression of phosphate-regulated genes was identified and cloned. This regulatory locus cloned from V. parahaemolyticus was shown to complement E. coli strains with defects in pho regulatory genes.

Citing Articles

Regulation of cell-wall morphology and growth encoded by plasmids in Shigella dysenteriae type 1.

Biswas D, Ghosh A, Kumar R World J Microbiol Biotechnol. 2014; 11(3):280-3.

PMID: 24414647 DOI: 10.1007/BF00367098.


Defining the niche of Vibrio parahaemolyticus during pre- and post-monsoon seasons in the coastal Arabian Sea.

Rehnstam-Holm A, Atnur V, Godhe A Microb Ecol. 2013; 67(1):57-65.

PMID: 24158690 DOI: 10.1007/s00248-013-0311-3.


ScrG, a GGDEF-EAL protein, participates in regulating swarming and sticking in Vibrio parahaemolyticus.

Kim Y, McCarter L J Bacteriol. 2007; 189(11):4094-107.

PMID: 17400744 PMC: 1913424. DOI: 10.1128/JB.01510-06.


Substrate specificity of the Escherichia coli outer membrane protease OmpP.

Hwang B, Varadarajan N, Li H, Rodriguez S, Iverson B, Georgiou G J Bacteriol. 2006; 189(2):522-30.

PMID: 17085556 PMC: 1797397. DOI: 10.1128/JB.01493-06.


Variable expression of extracellular polysaccharide in the marine bacterium Pseudomonas atlantica is controlled by genome rearrangement.

Bartlett D, Wright M, Silverman M Proc Natl Acad Sci U S A. 1988; 85(11):3923-7.

PMID: 16593937 PMC: 280332. DOI: 10.1073/pnas.85.11.3923.


References
1.
ZEN-YOJI H, Sakai S, TERAYAMA T, Kudo Y, Ito T, BENOKI M . Epidemiology, enteropathogenicity, and classification of Vi.rio parahaemolyticus. J Infect Dis. 1965; 115(5):436-44. DOI: 10.1093/infdis/115.5.436. View

2.
Sierra G . Hemolytic effect of a glycolipid produced by Pseudomonas aeruginosa. Antonie Van Leeuwenhoek. 1960; 26:189-92. DOI: 10.1007/BF02539004. View

3.
Kurioka S, LIU P . Effect of the hemolysin of Pseudomonas aeruginosa on phosphatides and on phospholipase c activity. J Bacteriol. 1967; 93(2):670-4. PMC: 276493. DOI: 10.1128/jb.93.2.670-674.1967. View

4.
Laemmli U . Cleavage of structural proteins during the assembly of the head of bacteriophage T4. Nature. 1970; 227(5259):680-5. DOI: 10.1038/227680a0. View

5.
Fairbanks G, Steck T, Wallach D . Electrophoretic analysis of the major polypeptides of the human erythrocyte membrane. Biochemistry. 1971; 10(13):2606-17. DOI: 10.1021/bi00789a030. View