Yıl: 2012 Cilt: 36 Sayı: 4 Sayfa Aralığı: 373 - 380 Metin Dili: İngilizce İndeks Tarihi: 29-07-2022

Deletion of polyphosphate kinase gene (ppk) has a stimulatory effect on actinorhodin production by Streptomyces coelicolor A3(2)

Öz:
Polyphosphate, which is synthesized by the enzyme polyP kinase (PPK), is an important energy and phosphate storage polymer that plays a crucial role in the regulation of adaptive responses of cells to physical and chemical stresses. In this work, the polyphosphate kinase gene (ppk) of Streptomyces coelicolor was deleted, and the eff ect of this mutation on actinorhodin and undecylprodigiosin biosynthesis was investigated. Deletion of the ppk gene had a stimulatory eff ect on actinorhodin production; the mutant strain produced about 5 times more antibiotic compared to the wild type strain at 120 h of growth. There was no difference in undecylprodigiosin production between the mutant and wild-type strains. In the presence of a selective antibiotic, the mutant strain could grow only on rich medium and could not sporulate effectively. Moreover, while the wild type strain was resistant, the mutant strain was sensitive to H2O2 in the conditions tested. Mutant characters were complemented by the ppk gene, which is cloned on a high copy number plasmid.
Anahtar Kelime: antibiotics bacteria polyphosphate kinase mutants polyphosphates genes production hydrogen peroxide Streptomyces coelicolor

Konular: Biyoloji
Belge Türü: Makale Makale Türü: Araştırma Makalesi Erişim Türü: Erişime Açık
  • 1. Brown MR, Kornberg A. Inorganic polyphosphate in the origin and survival of species. Proc Natl Acad Sci USA 101: 16085-87, 2004.
  • 2. Ahn K, Kornberg A. Polyphosphate kinase from Escherichia coli. J Biol Chem 265: 11734-39, 1990.
  • 3. Akiyama M, Crooke E, Kornberg A. An exopolyphosphatase of Escherichia coli: the enzyme and its ppx gene in a polyphosphate operon. J Biol Chem 268: 633-39, 1993.
  • 4. Kulaev IS, Vagabov VM. Polyphosphate metabolism in microorganisms. Adv Microb Physiol 24: 83-171, 1983.
  • 5. Phillips NFB, Hsien PC, Kowalczyk TH. Biochemistry, Biology, Biotechnology. In: Schroder HC, Muller WGE. eds. Inorganic Polyphosphates. Springer-Verlag; 1999: pp. 101-127.
  • 6. van Veen HW, Abee T, Kortstee GJJ et al. Generation of a proton motive force by the excretion of metal phosphate in the polyphosphate-accumulating Acinetobacter johnsonii strain 210A. J Biol Chem 269: 29509-29514, 1994.
  • 7. Shiba T, Tsutsumi K, Ishige K et al. Inorganic polyphosphate and polyphosphate kinase: their novel biological functions and applications. Biochemistry 65: 315-23, 2000.
  • 8. Kusano S, Ishihama A. Functional interaction of Escherichia coli RNA polymerase with inorganic polyphosphate. Genes Cells 2: 433-41, 1997.
  • 9. McInerney P, Taeko M, Toshikazu S. Inorganic polyphosphate interacts with ribosomes and promotes translation fi delity in vitro and in vivo. Mol Microbiol 60: 438-447, 2006.
  • 10. Rashid M, Rao NN, Kornberg A. Inorganic polyphosphate is required for motility of bacterial pathogens. J Bacteriol 182: 225-227, 2000.
  • 11. Rashid MH, Rumbaugh K, Passador L. Polyphosphate kinase is essential for biofi lm development, quorum sensing, and virulence of Pseudomonas aeruginosa. Proc Natl Acad Sci USA 97: 9636-9641, 2000.
  • 12. Kim L, Harwood A, Kimmel AR. Receptor-dependent and tyrosine phosphatase-mediated inhibition of GSK3 regulates cell fate choice. Developmental Cell 3: 523-532, 2002.
  • 13. Liras P, Asturias JA, Martin JF. Phosphate control sequences involved in transcriptional regulation of antibiotic biosynthesis. Trends Biotechnol 8: 184-189, 1990.
  • 14. Chouyekh H, Virolle MJ. The polyphosphate kinase plays a negative role in the control of antibiotic production in Streptomyces lividans. Mol Microbiol 43: 919-30, 2002.
  • 15. Ghorbel S, Kormanec J, Artus A et al. Transcriptional studies and regulatory interactions between the phoR-phoP operon and the phoU, mtpA, and ppk genes of Streptomyces lividans TK24. J Bacteriol 188: 677-686, 2006.
  • 16. MacNeil DJ, Gewain KM, Ruby CL et al. Analysis of Streptomyces avermitilis genes required for avermectin biosynthesis utilizing a novel integration vector. Gene 111: 61-68, 1992.
  • 17. Paget MS, Chamberlin L, Atrih A et al. Evidence that the extracytoplasmic function sigma factor sigmaE is required for normal cell wall structure in Streptomyces coelicolor A3 (2). J Bacteriol 181: 204-211, 1999.
  • 18. Hopwood DA, Bibb MJ, Chater KF et al. Genetic Manipulation of Streptomyces: A Laboratory Manual. John Innes Foundation, Norwich. 1985.
  • 19. Datsenko KA, Wanner BL. One-step inactivation of chromosomal genes in Escherichia coli K-12 using PCR products. Proc Natl Acad Sci USA 97: 6640-6645, 2000.
  • 20. Sambrook J, Fritsch EF, Maniatis T. Molecular Cloning: A Laboratory Manual. Cold Spring Harbor Laboratory Press, New York; 1989.
  • 21. Kieser T, Bibb MJ, Buttner MJ et al. Practical Streptomyces Genetics. The John Innes Foundation. Norwich; 2000.
  • 22. Gust B, Challis GL, Fowler K et al. PCR targeted Streptomyces gene replacement identifi es a protein domain needed for biosynthesis of the sesquiterpene soil odor geosmin. Proc Natl Acad Sci USA 100: 1541-1546, 2003.
  • 23. Hopwood DA, Malpartida F, Kieser HM et al. Production of ‘hybrid’ antibiotics by genetic engineering. Nature 314: 642- 644, 1985.
  • 24. Avignone RC, White J, Kuiper A et al. Carbon flux distribution in antibiotic-producing chemostat cultures of Streptomyces lividans. Metab Eng 4: 138-150, 2002.
  • 25. Kang SG, Jin W, Bibb M et al. Actinorhodin and undecylprodigiosin production in wild-type and relA mutant strains of Streptomyces coelicolor A3(2) grown in continuous culture. FEMS Microbiol Lett 168: 221-226, 1998.
  • 26. McDowall KJ, Thamchaipenet A, Hunter IS. Phosphate control of oxytetracycline production by Streptomyces rimosus is at the level of transcription from promoters overlapped by tandem repeats similar to those of the DNA-binding sites of the OmpR family. J Bacteriol 181: 3025-3032, 1999.
  • 27. Martin JF, Liras P, Demain AL. ATP and adenylate energy charge during phosphate-mediated control of antibiotic synthesis. Biochem Biophys Res Commun 83: 822-828, 1978.
  • 28. Lounes A, Lebrihi A, Benslimane C et al. Regulation of spiramycin synthesis in Streptomyces ambofaciens: effects of glucose and inorganic phosphate. Appl Microbiol Biotechnol 45: 204-211, 1996.
APA CAMCI YALIM İ, DORUK T, AVİCAN Ü, GEDİK TUNCA S (2012). Deletion of polyphosphate kinase gene (ppk) has a stimulatory effect on actinorhodin production by Streptomyces coelicolor A3(2). , 373 - 380.
Chicago CAMCI YALIM İrem,DORUK TUGRUL,AVİCAN Ümmehan,GEDİK TUNCA Sedef Deletion of polyphosphate kinase gene (ppk) has a stimulatory effect on actinorhodin production by Streptomyces coelicolor A3(2). (2012): 373 - 380.
MLA CAMCI YALIM İrem,DORUK TUGRUL,AVİCAN Ümmehan,GEDİK TUNCA Sedef Deletion of polyphosphate kinase gene (ppk) has a stimulatory effect on actinorhodin production by Streptomyces coelicolor A3(2). , 2012, ss.373 - 380.
AMA CAMCI YALIM İ,DORUK T,AVİCAN Ü,GEDİK TUNCA S Deletion of polyphosphate kinase gene (ppk) has a stimulatory effect on actinorhodin production by Streptomyces coelicolor A3(2). . 2012; 373 - 380.
Vancouver CAMCI YALIM İ,DORUK T,AVİCAN Ü,GEDİK TUNCA S Deletion of polyphosphate kinase gene (ppk) has a stimulatory effect on actinorhodin production by Streptomyces coelicolor A3(2). . 2012; 373 - 380.
IEEE CAMCI YALIM İ,DORUK T,AVİCAN Ü,GEDİK TUNCA S "Deletion of polyphosphate kinase gene (ppk) has a stimulatory effect on actinorhodin production by Streptomyces coelicolor A3(2)." , ss.373 - 380, 2012.
ISNAD CAMCI YALIM, İrem vd. "Deletion of polyphosphate kinase gene (ppk) has a stimulatory effect on actinorhodin production by Streptomyces coelicolor A3(2)". (2012), 373-380.
APA CAMCI YALIM İ, DORUK T, AVİCAN Ü, GEDİK TUNCA S (2012). Deletion of polyphosphate kinase gene (ppk) has a stimulatory effect on actinorhodin production by Streptomyces coelicolor A3(2). Turkish Journal of Biology, 36(4), 373 - 380.
Chicago CAMCI YALIM İrem,DORUK TUGRUL,AVİCAN Ümmehan,GEDİK TUNCA Sedef Deletion of polyphosphate kinase gene (ppk) has a stimulatory effect on actinorhodin production by Streptomyces coelicolor A3(2). Turkish Journal of Biology 36, no.4 (2012): 373 - 380.
MLA CAMCI YALIM İrem,DORUK TUGRUL,AVİCAN Ümmehan,GEDİK TUNCA Sedef Deletion of polyphosphate kinase gene (ppk) has a stimulatory effect on actinorhodin production by Streptomyces coelicolor A3(2). Turkish Journal of Biology, vol.36, no.4, 2012, ss.373 - 380.
AMA CAMCI YALIM İ,DORUK T,AVİCAN Ü,GEDİK TUNCA S Deletion of polyphosphate kinase gene (ppk) has a stimulatory effect on actinorhodin production by Streptomyces coelicolor A3(2). Turkish Journal of Biology. 2012; 36(4): 373 - 380.
Vancouver CAMCI YALIM İ,DORUK T,AVİCAN Ü,GEDİK TUNCA S Deletion of polyphosphate kinase gene (ppk) has a stimulatory effect on actinorhodin production by Streptomyces coelicolor A3(2). Turkish Journal of Biology. 2012; 36(4): 373 - 380.
IEEE CAMCI YALIM İ,DORUK T,AVİCAN Ü,GEDİK TUNCA S "Deletion of polyphosphate kinase gene (ppk) has a stimulatory effect on actinorhodin production by Streptomyces coelicolor A3(2)." Turkish Journal of Biology, 36, ss.373 - 380, 2012.
ISNAD CAMCI YALIM, İrem vd. "Deletion of polyphosphate kinase gene (ppk) has a stimulatory effect on actinorhodin production by Streptomyces coelicolor A3(2)". Turkish Journal of Biology 36/4 (2012), 373-380.