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Genome Mining of the Hitachimycin Biosynthetic Gene Cluster: Involvement of a Phenylalanine‐2,3‐aminomutase in Biosynthesis
Authors:Prof. Dr. Fumitaka Kudo  Koichi Kawamura  Asuka Uchino  Dr. Akimasa Miyanaga  Mario Numakura  Ryuichi Takayanagi  Prof. Dr. Tadashi Eguchi
Affiliation:1. Department of Chemistry, Tokyo Institute of Technology, 2‐12‐1 O‐okayama, Meguro‐ku, Tokyo 152‐8551 (Japan);2. Department of Chemistry and Materials Science, Tokyo Institute of Technology, 2‐12‐1 O‐okayama, Meguro‐ku, Tokyo 152‐8551 (Japan)
Abstract:Hitachimycin is a macrolactam antibiotic with (S)‐β‐phenylalanine (β‐Phe) at the starter position of its polyketide skeleton. To understand the incorporation mechanism of β‐Phe and the modification mechanism of the unique polyketide skeleton, the biosynthetic gene cluster for hitachimycin in Streptomyces scabrisporus was identified by genome mining. The identified gene cluster contains a putative phenylalanine‐2,3‐aminomutase (PAM), five polyketide synthases, four β‐amino‐acid‐carrying enzymes, and a characteristic amidohydrolase. A hitA knockout mutant showed no hitachimycin production, but antibiotic production was restored by feeding with (S)‐β‐Phe. We also confirmed the enzymatic activity of the HitA PAM. The results suggest that the identified gene cluster is responsible for the biosynthesis of hitachimycin. A plausible biosynthetic pathway for hitachimycin, including a unique polyketide skeletal transformation mechanism, is proposed.
Keywords:antibiotics  biosynthesis  genome mining  hitachimycin  macrolactam polyketide  phenylalanine‐2,3‐aminomutase
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