辅因子
ATP合酶
化学
生物化学
生物合成
立体化学
酶
组合化学
作者
Martin Dippe,Wolfgang Brandt,H. Rost,Andrea Porzel,Jürgen Schmidt,Ludger A. Wessjohann
摘要
S-Adenosylmethionine (SAM) synthase was engineered for biocatalytic production of SAM and long-chain analogues by rational re-design. Substitution of two conserved isoleucine residues extended the substrate spectrum of the enzyme to artificial S-alkylhomocysteines. The variants proved to be beneficial in preparative synthesis of SAM (and analogues) due to a much reduced product inhibition.
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