Identification of gntK, a gene required for the methylation of purpurosamine C-6′ in gentamicin biosynthesis

Gentamicin and sisomicin are two different aminoglycoside antibiotics. The comparison of their chemical structure and biosynthetic gene clusters, coupled with bioinformatic analysis, suggested that the gntK gene would be associated with methylation. The gntK gene fragment in M. purpurea G1008 was in...

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Veröffentlicht in:Journal of general and applied microbiology 2012, Vol.58(5), pp.349-356
Hauptverfasser: Hong, Wenrong, Yan, Lingbin
Format: Artikel
Sprache:eng
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Zusammenfassung:Gentamicin and sisomicin are two different aminoglycoside antibiotics. The comparison of their chemical structure and biosynthetic gene clusters, coupled with bioinformatic analysis, suggested that the gntK gene would be associated with methylation. The gntK gene fragment in M. purpurea G1008 was inactivated by genetic engineering and its mutant strain M. purpurea GK1101 (ΔgntK) was screened. The metabolites of G1008 and GK1101 was analyzed by HPLC-MS, which revealed that GK1101 no longer produced gentamicin C1 or C2, while mainly synthesizing gentamicin C1a, and the production of C1a increased significantly. This indicated that the metabolic flow for the gentamicin C1 and C2 biosynthesis was blocked by disrupting the gntK gene, which substantiated that the gntK gene encoded the enzyme that catalyzes the methylation of purpurosamine C-6′. The mutant GK1101 has good prospects for industrial application. In addition, our study provides information that can be used to clarify the function of a single gene and simplify the targeted genetic breeding of important pharmaceutical microorganisms.
ISSN:0022-1260
1349-8037
DOI:10.2323/jgam.58.349