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10.1002/cbic.200500425

http://scihub22266oqcxt.onion/10.1002/cbic.200500425
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16511823!7162017!16511823
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suck abstract from ncbi


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pmid16511823      Chembiochem 2006 ; 7 (3): 471-7
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  • Deciphering the biosynthetic codes for the potent anti-SARS-CoV cyclodepsipeptide valinomycin in Streptomyces tsusimaensis ATCC 15141 #MMPMID16511823
  • Cheng YQ
  • Chembiochem 2006[Mar]; 7 (3): 471-7 PMID16511823show ga
  • Valinomycin was recently reported to be the most potent agent against severe acute respiratory-syndrome coronavirus (SARS-CoV) in infected Vero E6 cells. Aimed at generating analogues by metabolic engineering, the valinomycin biosynthetic gene cluster has been cloned from Streptomyces tsusimaensis ATCC 15141. Targeted disruption of a nonribosomal peptide synthetase (NRPS) gene abolishes valinomycin production, which confirms its predicted nonribosomal-peptide origin. Sequence analysis of the NRPS system reveals four distinctive modules, two of which contain unusual domain organizations that are presumably involved in the generation of biosynthetic precursors D-alpha-hydroxyisovaleric acid and L-lactic acid. The respective adenylation domains in these two modules contain novel substrate-specificity-conferring codes that might specify for a class of hydroxyl acids for the biosynthesis of the depsipeptide natural products.
  • |Animals[MESH]
  • |Anti-Bacterial Agents/*biosynthesis[MESH]
  • |Antiviral Agents/*metabolism/pharmacology[MESH]
  • |Chlorocebus aethiops[MESH]
  • |Genes, Bacterial[MESH]
  • |Molecular Sequence Data[MESH]
  • |Multigene Family[MESH]
  • |Severe acute respiratory syndrome-related coronavirus/*drug effects[MESH]
  • |Streptomyces/genetics/*metabolism[MESH]
  • |Valinomycin/*biosynthesis[MESH]


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