Department of Chemistry, Boston College, Merkert Chemistry Center, Chestnut Hill, MA 02467, USA.
Curr Opin Chem Biol. 2009 Oct;13(4):460-8. doi: 10.1016/j.cbpa.2009.06.013. Epub 2009 Jul 19.
The prosthetic group 4-methylideneimidazole-5-one (MIO) is the catalytic component of the ammonia lyase class of enzymes. This family is responsible for the processing of amino acids in a variety of metabolic pathways through the elimination of ammonia to form unsaturated products. Recently, new chemistry has been attributed to this family with the discovery of MIO-based aminomutases. The mechanism of electrophilic chemistry catalyzed by MIO-based enzymes has been investigated for several decades. Recent X-ray crystal structures of members of the family have provided novel insight into the molecular basis for catalysis and substrate recognition. In addition, the inclusion of aminomutases in natural product biosynthetic pathways has spurned recent advances toward rational engineering and chemoenzymatic applications.
辅基 4-亚甲基咪唑-5-酮(MIO)是氨裂解酶类酶的催化成分。该家族负责通过消除氨来形成不饱和产物,从而在各种代谢途径中处理氨基酸。最近,由于发现基于 MIO 的氨突变酶,该家族有了新的化学性质。基于 MIO 的酶催化的亲电化学机制已经研究了几十年。该家族成员的最近 X 射线晶体结构为催化和底物识别的分子基础提供了新的见解。此外,将氨突变酶纳入天然产物生物合成途径中,推动了最近在合理工程和化学酶应用方面的进展。