Identification and Functional Analysis of the putAP Genes Encoding Vibrio vulnificus Proline Dehydrogenase and Proline Permease

  • Kim, Hye-Jin (Department of Food Science and Technology, Department of Molecular Biotechnology, Institute of Biotechnology, Chonnam National University) ;
  • Lee, Jeong-Hyun (Department of Food Science and Technology, Department of Molecular Biotechnology, Institute of Biotechnology, Chonnam National University) ;
  • Rhee, Jee-Eun (Department of Food Science and Technology, Department of Molecular Biotechnology, Institute of Biotechnology, Chonnam National University) ;
  • Jeong, Hye-Sook (Department of Food Science and Technology, Department of Molecular Biotechnology, Institute of Biotechnology, Chonnam National University) ;
  • Choi, Hyun-Kyung (Department of Food Science and Technology, Department of Molecular Biotechnology, Institute of Biotechnology, Chonnam National University) ;
  • Chung, Hee-Jong (Department of Food Science and Technology, Department of Molecular Biotechnology, Institute of Biotechnology, Chonnam National University) ;
  • Ryu, Sang-Ryeol (Department of Food Science and Technology, School of Agricultural Biotechnology, Seoul National University) ;
  • Choi, Sang-Ho (Department of Food Science and Technology, Department of Molecular Biotechnology, Institute of Biotechnology, Chonnam National University)
  • Published : 2002.04.01

Abstract

The pathogenic marine bacterium Vibrio vulnificus is the causative agent of food-borne diseases such as life-threatening septicemia. To better understand this organism's strategies to survive osmotic stress, a mutant that was more sensitive to high osmolarity was screened from a library of mutants constructed by a random transposon mutagenesis. By a transposon-tagging method, putAP genes encoding a proline dehydrogenase and a proline permease were identified and cloned from V. vulnificus. The amino acid sequences deduced from nucleotide sequences of putAP from V. vulnificus were 38 to $59\%$ similar to those of PutA and PutP reported from other Enterobacteriaceae. Functions of putAP genes were assessed by the construction of mutants, whose putAP genes were inactivated by allelic exchanges. When proline as the sole carbon or nitrogen source was used, the putA mutant was not able to grow to the substantial level, revealing the proline dehydrogenase is the only enzyme for metabolic conversion of proline into other amino acids. Although the growth rate of the putP mutant on proline as the sole carbon or nitrogen source was significantly reduced, the mutant still grew. This indicated that at least one more proline permease is produced by V. vulnificus. The putP mutant decreased approximately $2-log_10$ CFU/ml after a hyperosmotic challenge, while the parent strain decreased approximately $l-log_10$ CFU/ml. This result suggests that the gene product of putP contributes to the osmotic tolerance of V. vulnificus.

Keywords

References

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