Wang K C, Ohnuma S
University of California, San Francisco, School of Medicine, San Francisco, CA 94143, USA.
Biochim Biophys Acta. 2000 Dec 15;1529(1-3):33-48. doi: 10.1016/s1388-1981(00)00136-0.
Isoprenyl diphosphate synthases catalyze consecutive condensations of isopentenyl diphosphates with allylic primer substrates to form linear backbones for all isoprenoid compounds including cholesterol. These synthases are classified according to the final chain length of their end products and the stereochemistry of the newly formed double bonds. Mutagenesis and X-ray crystallography data have uncovered the basic catalytic and chain length determination mechanisms of E-isoprenyl diphosphate synthases and shed light on their possible evolutionary course. Although much less is known about the Z-isoprenyl diphosphate synthase family, successful cloning and subsequent crystallizations in the near future will no doubt bring more insight as researchers begin to unravel the essential components and precise reaction mechanisms of this cellular machinery.
异戊二烯基二磷酸合酶催化异戊烯基二磷酸与烯丙基引物底物的连续缩合反应,以形成包括胆固醇在内的所有类异戊二烯化合物的线性骨架。这些合酶根据其终产物的最终链长和新形成双键的立体化学进行分类。诱变和X射线晶体学数据揭示了E-异戊二烯基二磷酸合酶的基本催化和链长确定机制,并为其可能的进化过程提供了线索。尽管对Z-异戊二烯基二磷酸合酶家族的了解要少得多,但随着研究人员开始揭示这种细胞机制的基本组成部分和精确反应机制,在不久的将来成功克隆并随后进行结晶无疑将带来更多的见解。