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Different Effects of Acidic pH Shock on the Prodiginine Production in Streptomyces coelicolor M511 and SJM1 Mutants

  • Mo, SangJoon (Biosafety & Validation Center, Clinical Trial Institute, Dankook University) ;
  • Kim, Jae-Heon (Department of Microbiology, College of Natural Science, Dankook University) ;
  • Oh, Chung-Hun (Biosafety & Validation Center, Clinical Trial Institute, Dankook University)
  • Received : 2013.07.22
  • Accepted : 2013.08.10
  • Published : 2013.10.28

Abstract

The changes in prodiginines productions caused by pH shock culture of Streptomyces coelicolor strains were estimated. In Streptomyces coelicolor M511, undecylprodiginine and streptorubin B productions increased 1.8-fold (37.22 mg/g) and 2.5-fold (18.61 mg/g), respectively, by pH shock (from 7.2 to 4.0). In contrast, this resulted in the significantly decreased prodigignines production in the redP deletion mutant SJM1; 3.7-fold for undecylprodiginine, 4.4-fold for streptorubin B, 5.2-fold for methylundecylprodiginine, and 6.4-fold for methyldodecylundecylprodiginine, respectively. RT-PCR analyses showed that, during pH shock, expression of redD, the transcription activator gene, was increased while the expression of fabH, the decarboxylative condensation enzyme gene in fatty acid biosynthesis, was decreased in both strains. The enhanced redD expression was in good accordance with the increased total prodiginines production of M511. However, for SJM1 mutant, the decrease of fabH expression occurred more strikingly, such that it became almost completely turned off during acidic pH shock culture. Therefore, a down-regulation of fabH was considered to be the cause of decreased amount of total prodiginines produced, although redD expression was high in SJM1 mutant.

Keywords

References

  1. Azuma T, Watanabe N, Yagisawa H, Hirata K, Iwamura M, Kobayashi Y. 2000. Induction of apoptosis of activated murine splenic T cells by cycloprodigiosin hydrochloride, a novel immunosuppressant. Immunopharmacology 46: 29-37. https://doi.org/10.1016/S0162-3109(99)00153-8
  2. Cerdeno AM, Bibb MJ, Challis GL. 2001. Analysis of the prodiginine biosynthesis gene cluster of Streptomyces coelicolor A3(2): new mechanisms for chain initiation and termination in modular multienzymes. Chem. Biol. 8: 817-829. https://doi.org/10.1016/S1074-5521(01)00054-0
  3. Dairi K, Tripathy S, Attardo G, Lavallee J-F. 2006. Two-step synthesis of the bipyrrole precursor of prodigiosins. Tetrahedron Lett. 47: 2605-2606. https://doi.org/10.1016/j.tetlet.2006.02.035
  4. D'Alessio R, Bargiotti A, Carlin O, Colotta F, Ferrari M, Gnocchi P, et al. 2000. Synthesis and immunosuppresive activity of novel prodigiosin derivatives. J. Med. Chem. 43: 2557-2565. https://doi.org/10.1021/jm001003p
  5. Furstner A. 2003. Chemistry and biology of roseophilin and the prodigiosin alkaloids: a survey of the last 2500 years. Angew. Chem. Int. Ed. Engl. 42: 3582-3603. https://doi.org/10.1002/anie.200300582
  6. Hayes A, Hobbs G, Smith CP, Oliver SG, Butler PR. 1997. Environmental signals triggering methylenomycin production by Streptomyces coelicolor A3(2). J. Bacteriol. 179: 5511-5515. https://doi.org/10.1128/jb.179.17.5511-5515.1997
  7. Kaiser D, Losick R. 1993. How and why bacteria talk to each other. Cell 73: 873-885. https://doi.org/10.1016/0092-8674(93)90268-U
  8. Kim CJ, Chang YK, Chun GT, Jeong YH, Lee SJ. 2001. Continuous culture of immobilized Streptomyces cells for Kasugamycin production. Biotechnol. Prog. 17: 453-461. https://doi.org/10.1021/bp010020k
  9. Kim YJ, Song JY, Moon MH, Smith CP, Hong S-K, Chang YK. 2007. pH shock induces overexpression of regulatory and biosynthetic genes for actinorhodin production in Streptomyces coelicolor A3(2). Appl. Microbiol. Biotechnol. 76: 1119-1130. https://doi.org/10.1007/s00253-007-1083-9
  10. Kim YJ, Moon MH, Song JY, Smith CP, Hong SK, Chang YK. 2008. Acidic pH shock induces the expressions of a wide range of stress-response genes. BMC Genomics 9: 604. https://doi.org/10.1186/1471-2164-9-604
  11. Mo S. 2010. Enhanced prodiginines production in Streptomyces coelicolor M511 by stress of acidic pH shock. Kor. J. Microbiol. Biotechnol. 38: 273-277.
  12. Mo S, Kim BS, Reynolds KA. 2005. Production of branchedchain alkylprodiginines in S. coelicolor by replacement of the 3-ketoacyl ACP synthase III initiation enzyme, RedP. Chem. Biol. 12: 191-200. https://doi.org/10.1016/j.chembiol.2004.11.006
  13. Mo S, Sydor PK, Corre C, Alhamadsheh MM, Stanley AE, Haynes SW, et al. 2008. Elucidation of the Streptomyces coelicolor pathway to 2-undecylpyrrole, a key intermediate in undecylprodiginine and streptorubin B biosynthesis. Chem. Biol. 15: 137-148. https://doi.org/10.1016/j.chembiol.2007.11.015
  14. Mortellaro A, Songia S, Gnocchi P, Ferrari M, Fornasiero C, D'Alessio R, et al. 1999. New immunosuppresive drug PNU156804 blocks IL-2-dependent proliferation and NFkappa B and AP-1 activation. J. Immunol. 162: 7102-7109.
  15. Sevcikova B, Kormanec J. 2004. Differential production of two antibiotics of Streptomyces coelicolor A3(2), actinorhodin and undecylprodigiosin, upon salt stress conditions. Arch. Microbiol. 181: 384-389. https://doi.org/10.1007/s00203-004-0669-1
  16. Stanley AE, Walton LJ, Kourdi-Zerikly M, Corre C, Challis GL. 2006. Elucidation of the Streptomyces coelicolor pathway to 4-methoxy-2,2'-bipyrrole-5-carboxaldehyde, an intermediate in prodiginine biosynthesis Chem. Commun. (Camb). 38: 3981-3938.
  17. Tsao SW, Rudd BA, He XG, Chang CJ, Floss HG. 1985. Identification of a red pigment from Streptomyces coelicolor A3(2) as a mixture of prodigiosin derivatives. J. Antibiot. 38: 128-131. https://doi.org/10.7164/antibiotics.38.128
  18. White J, Bibb M. 1997. bldA dependence of undecylprodigiosin production in Streptomyces coelicolor A3(2) involves a pathwayspecific regulatory cascade. J. Bacteriol. 179: 627-633. https://doi.org/10.1128/jb.179.3.627-633.1997

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