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. 1984 Jul;48(1):43–47. doi: 10.1128/aem.48.1.43-47.1984

Stabilization of a histidine-producing strain of Serratia marcescens.

M Sugiura, M Kisumi
PMCID: PMC240301  PMID: 6383217

Abstract

A decrease in histidine productivity was observed during subculture of a histidine-producing strain of Serratia marcescens. The decrease was accompanied by an increase in the number of wild-type revertants. Adenine accelerated the growth of producing strain HT-2892 to nearly equal that of revertants, and histidine production was stable because the depletion of ATP in strain HT-2892 was restored by adenine. To increase the intracellular ATP content, mutants resistant to 6-methylpurine, an antagonist of adenine, were isolated from strain HT-2892. 6-Methylpurine-resistant mutant MPr90 grew more rapidly than the parent producing strain and produced L-histidine stably, even when it was subjected to subculture in medium without adenine. ATP depletion was restored in strain MPr90, probably owing to the derepression of adenylosuccinate synthetase in AMP biosynthesis.

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Selected References

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

  1. Benson C. E., Love S. H., Remy C. N. Inhibition of de novo purine biosynthesis and interconversion by 6-methylpurine in Escherichia coli. J Bacteriol. 1970 Mar;101(3):872–880. doi: 10.1128/jb.101.3.872-880.1970. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Cole H. A., Wimpenny J. W., Hughes D. E. The ATP pool in Escherichia coli. I. Measurement of the pool using modified luciferase assay. Biochim Biophys Acta. 1967;143(3):445–453. doi: 10.1016/0005-2728(67)90050-3. [DOI] [PubMed] [Google Scholar]
  3. Fischer H. E., Muirhead K. M., Bishop S. H. Adenylosuccinate synthetase (rabbit muscle, heart, and liver). Methods Enzymol. 1978;51:207–213. doi: 10.1016/s0076-6879(78)51029-x. [DOI] [PubMed] [Google Scholar]
  4. Johnston H. M., Roth J. R. Histidine mutants requiring adenine: selection of mutants with reduced hisG expression in Salmonella typhimurium. Genetics. 1979 May;92(1):1–15. doi: 10.1093/genetics/92.1.1. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Kisumi M., Nakanishi N., Takagi T., Chibata I. L-Histidine production by histidase-less regulatory mutants of Serratia marcescens constructed by transduction. Appl Environ Microbiol. 1977 Nov;34(5):465–472. doi: 10.1128/aem.34.5.465-472.1977. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. LOWRY O. H., ROSEBROUGH N. J., FARR A. L., RANDALL R. J. Protein measurement with the Folin phenol reagent. J Biol Chem. 1951 Nov;193(1):265–275. [PubMed] [Google Scholar]
  7. Matsumoto H., Hosogaya S., Suzuki K., Tazaki T. Arginine gene cluster of Serratia marcescens. Jpn J Microbiol. 1975 Feb;19(1):35–44. doi: 10.1111/j.1348-0421.1975.tb00845.x. [DOI] [PubMed] [Google Scholar]
  8. Matsumoto H., Tazaki T., Hosogaya S. A generalized transducing phage of Serratia marcescens. Jpn J Microbiol. 1973 Nov;17(6):473–479. doi: 10.1111/j.1348-0421.1973.tb00933.x. [DOI] [PubMed] [Google Scholar]
  9. Pendyala L., Smyth J., Wellman A. M. Nature of 6-methylpurine inhibition and characterization of two 6-methylpurine-resistant mutants of Neurospora crassa. J Bacteriol. 1979 Jan;137(1):248–255. doi: 10.1128/jb.137.1.248-255.1979. [DOI] [PMC free article] [PubMed] [Google Scholar]

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