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. 1975 Oct;124(1):567–569. doi: 10.1128/jb.124.1.567-569.1975

Mutants Defective in Binding Activity for Cyclic Adenosine 3′,5′-Monophosphate in Vibrio parahaemolyticus

Shiro Iuchi 1, Yoneo Kubota 1, Shuji Tanaka 1
PMCID: PMC235929  PMID: 170251

Abstract

Mutants of Vibrio parahaemolyticus defective in binding activity for adenosine 3′,5′-cyclic monophosphate are described. They were selected with medium containing the nucleotide together with starch.

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Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Ackerman R. S., Cozzarelli N. R., Epstein W. Accumulation of toxic concentrations of methylglyoxal by wild-type Escherichia coli K-12. J Bacteriol. 1974 Aug;119(2):357–362. doi: 10.1128/jb.119.2.357-362.1974. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. De Robertis E. M., Jr, Judewicz R. D., Torres H. N. On the control mechanism of bacterial growth by cyclic adenosine 3',5'-monophosphate. Biochem Biophys Res Commun. 1973 Dec 10;55(3):758–764. doi: 10.1016/0006-291x(73)91209-6. [DOI] [PubMed] [Google Scholar]
  3. Emmer M., deCrombrugghe B., Pastan I., Perlman R. Cyclic AMP receptor protein of E. coli: its role in the synthesis of inducible enzymes. Proc Natl Acad Sci U S A. 1970 Jun;66(2):480–487. doi: 10.1073/pnas.66.2.480. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Judewicz N. D., De Robertis E. M., Jr, Torres H. N. Inhibition of Escherichia coli growth by cyclic adenosine 3', 5'-monophosphate. Biochem Biophys Res Commun. 1973 Jun 19;52(4):1257–1262. doi: 10.1016/0006-291x(73)90636-0. [DOI] [PubMed] [Google Scholar]
  5. Matsumoto K., Iuchi S., Fujisawa A., Tanaka S. Enrichment of mutants lacking the phosphoenolpyruvate-dependent phosphotransferase system of Vibrio parahaemolyticus by screening with methyl-alpha-D-glucoside. J Bacteriol. 1974 Aug;119(2):632–634. doi: 10.1128/jb.119.2.632-634.1974. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Perlman R. L., Pastan I. Pleiotropic deficiency of carbohydrate utilization in an adenyl cyclase deficient mutant of Escherichia coli. Biochem Biophys Res Commun. 1969 Sep 24;37(1):151–157. doi: 10.1016/0006-291x(69)90893-6. [DOI] [PubMed] [Google Scholar]
  7. Tanaka S., Iuchi S. Induction and repression of an extracellular proteinase in Vibrio parahaemolyticus. Biken J. 1971 Jun;14(2):81–96. [PubMed] [Google Scholar]
  8. Yokota T., Gots J. S. Requirement of adenosine 3', 5'-cyclic phosphate for flagella formation in Escherichia coli and Salmonella typhimurium. J Bacteriol. 1970 Aug;103(2):513–516. doi: 10.1128/jb.103.2.513-516.1970. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Yokota T., Kuwahara S. Adenosine 3',5'-cyclic monophosphate-deficient mutants of Vibrio cholerae. J Bacteriol. 1974 Oct;120(1):106–113. doi: 10.1128/jb.120.1.106-113.1974. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Zubay G., Schwartz D., Beckwith J. Mechanism of activation of catabolite-sensitive genes: a positive control system. Proc Natl Acad Sci U S A. 1970 May;66(1):104–110. doi: 10.1073/pnas.66.1.104. [DOI] [PMC free article] [PubMed] [Google Scholar]

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