TY - JOUR
T1 - Cyclopentane-forming di/sesterterpene synthases
T2 - Widely distributed enzymes in bacteria, fungi, and plants
AU - Minami, Atsushi
AU - Ozaki, Taro
AU - Liu, Chengwei
AU - Oikawa, Hideaki
N1 - Funding Information:
This work was nancially supported by Grants-in-Aid for Scientic Research from the Ministry of Education, Culture, Sports, Science and Technology, Japan (JSPS KAKENHI Grant Number JP15H01835 (H. O.), JP16H03277 (A. M.), and JP16H06446 (A. M.)).
Publisher Copyright:
© 2018 The Royal Society of Chemistry.
PY - 2018/12
Y1 - 2018/12
N2 - Covering: 2000 to 2018 In the late 1960s, structurally unique fusicoccane- and ophiobolane-type di/sesterterpenes were isolated and their homologs were found to be widely distributed in various organisms. Nearly a half century later, the first terpene synthase PaFS was identified, which triggered the discovery of a number of di/sesterterpene synthases, which were named as cyclopentane-forming terpene synthases (CPF-TSs). In the past 10 years, CPF-TSs have emerged as a new type of class I terpene synthases, which afford di/sesterterpenes with characteristic polycyclic molecular skeletons; they catalyze two different types of cyclizations, defined as type A and B, which are relevant to the initial cyclization mode of a polyprenyl diphosphate. This review summarizes the characteristic features of CPF-TSs from various sources and detailed cyclization mechanisms; we have also discussed the structural diversification strategy of these novel enzymes.
AB - Covering: 2000 to 2018 In the late 1960s, structurally unique fusicoccane- and ophiobolane-type di/sesterterpenes were isolated and their homologs were found to be widely distributed in various organisms. Nearly a half century later, the first terpene synthase PaFS was identified, which triggered the discovery of a number of di/sesterterpene synthases, which were named as cyclopentane-forming terpene synthases (CPF-TSs). In the past 10 years, CPF-TSs have emerged as a new type of class I terpene synthases, which afford di/sesterterpenes with characteristic polycyclic molecular skeletons; they catalyze two different types of cyclizations, defined as type A and B, which are relevant to the initial cyclization mode of a polyprenyl diphosphate. This review summarizes the characteristic features of CPF-TSs from various sources and detailed cyclization mechanisms; we have also discussed the structural diversification strategy of these novel enzymes.
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U2 - 10.1039/c8np00026c
DO - 10.1039/c8np00026c
M3 - Review article
C2 - 29855001
AN - SCOPUS:85058104628
SN - 0265-0568
VL - 35
SP - 1330
EP - 1346
JO - Natural Product Reports
JF - Natural Product Reports
IS - 12
ER -