4.8 Article

Phosphate control over nitrogen metabolism in Streptomyces coelicolor: direct and indirect negative control of glnR, glnA, glnII and amtB expression by the response regulator PhoP

Journal

NUCLEIC ACIDS RESEARCH
Volume 37, Issue 10, Pages 3230-3242

Publisher

OXFORD UNIV PRESS
DOI: 10.1093/nar/gkp162

Keywords

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Funding

  1. 'Comision Interministerial de Ciencia y Tecnologia' [BIO2003-01489, BIO2006-14853-C02-01]
  2. 'Ministerio de Ciencia e Innovacion', Madrid [GEN2003-20245-C09- 01]
  3. AECID (Agencia Espanola de Cooperacion Internacional para el Desarrollo), 'Ministerio de Asuntos Exteriores y de Cooperacion', Madrid [A/010257/07]
  4. ERA-NET SySMO Project [GEN2006-27745-E/SYS]
  5. European Union [ACTINOGEN LSHM-CT-2004- 005224)]
  6. Ministerio de Ciencia e Innovacion (Spain)
  7. F. P. I. program (Ministerio de Ciencia e Innovacion, Spain)

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Bacterial growth requires equilibrated concentration of C, N and P sources. This work shows a phosphate control over the nitrogen metabolism in the model actinomycete Streptomyces coelicolor. Phosphate control of metabolism in Streptomyces is exerted by the two component system PhoR-PhoP. The response regulator PhoP binds to well-known PHOboxescomposed of direct repeat units (DRus). PhoP binds to the glnR promoter, encoding the major nitrogen regulator as shown by EMSA studies, but not to the glnRII promoter under identical experimental conditions. PhoP also binds to the promoters of glnA and glnII encoding two glutamine synthetases, and to the promoter of the amtB-glnK-glnD operon, encoding an ammonium transporter and two putative nitrogen sensing/regulatory proteins. Footprinting analyses revealed that the PhoP-binding sequence overlaps the GlnR boxes in both glnA and glnII. Information theory quantitative analyses of base conservation allowed us to establish the structure of the PhoP-binding regions in the glnR, glnA, glnII and amtB genes. Expression studies using luxAB as reporter showed that PhoP represses the above mentioned nitrogen metabolism genes. A mutant deleted in PhoP showed increased expression of the nitrogen metabolism genes. The possible conservation of phosphate control over nitrogen metabolism in other microorganisms is discussed.

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