| Literature DB >> 27311629 |
Yuki Inahashi1, Taro Shiraishi2, Kaia Palm3,4, Yoko Takahashi3, Satoshi Ōmura3, Tomohisa Kuzuyama2, Takuji Nakashima5.
Abstract
Trehangelins are trehalose angelates discovered from endophytic actinomycete Polymorphospora rubra K07-0510. We identified the trehangelin biosynthetic gene cluster, including genes that encode a glycoside hydrolase-like protein (thgC), α-amylase (thgD), 3-ketoacyl-ACP synthase III (thgI), 3-ketoacyl-ACP reductase (thgK), enoyl-CoA hydratase (thgH) and acyl transferase (thgJ). Heterologous expression of thgH, thgI, thgJ and thgK confirmed the importance of these genes in the biosynthesis of trehangelin A. Enzymatic activity studies showed that ThgI catalyses the condensation of acetyl-CoA and methylmalonyl-CoA to 2-methylacetoacetyl-CoA (MAA-CoA), ThgK catalyses NADPH-dependent reduction of MAA-CoA to 3-hydroxy-2-methylbutyryl-CoA (HMB-CoA) and ThgH catalyses the dehydration of HMB-CoA to angelyl-CoA (AN-CoA). This is the first report on the elucidation of the enzymatic formation of AN-CoA.Entities:
Keywords: angelate; angelyl-CoA; biosynthesis; endophytic actinomycete; natural products; trehangelin
Mesh:
Substances:
Year: 2016 PMID: 27311629 DOI: 10.1002/cbic.201600208
Source DB: PubMed Journal: Chembiochem ISSN: 1439-4227 Impact factor: 3.164