Recent advances in methyltransferase biocatalysis

被引:96
作者
Bennett, Matthew R.
Shepherd, Sarah A.
Cronin, Victoria A.
Micklefield, Jason [1 ]
机构
[1] Univ Manchester, Sch Chem, 131 Princess St, Manchester M1 7DN, Lancs, England
基金
英国生物技术与生命科学研究理事会;
关键词
ADENOSYL-L-METHIONINE; DEPENDENT O-METHYLTRANSFERASE; CRYSTAL-STRUCTURE; ENZYMATIC TRANSFORMATION; N-METHYLTRANSFERASE; PROTEIN METHYLATION; BIOSYNTHESIS; ENZYMES; SAM; DISCOVERY;
D O I
10.1016/j.cbpa.2017.01.020
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
S-adenosyl-L-methionine-dependent methyltransferses are ubiquitous in nature, methylating a vast range of small molecule metabolites, as well as biopolymers. This review covers the recent advances in the development of methyltransferase enzymes for synthetic applications, focusing on the methyltransferase catalyzed transformations with S-adenosyl methionine analogs, as well as non-native substrates. We discuss how metabolic engineering approaches have been used to enhance S-adenosyl methionine production in vivo. Enzymatic approaches that enable the more efficient generation of S-adenosyl methionine analogs, including more stable analogs, will also be described; this has expanded the biocatalytic repertoire of methyltransferases from methylation to a broader range of alkylation reactions. The review also examines how the selectivity of the methyltransferase enzymes can be improved through structure guided mutagenesis approaches. Finally, we will discuss how methyltransferases can be deployed in multi-enzyme cascade reactions and suggest future challenges and avenues for further investigation.
引用
收藏
页码:97 / 106
页数:10
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