TY - JOUR
T1 - Microbial-type terpene synthase genes occur widely in nonseed land plants, but not in seed plants
AU - Jia, Qidong
AU - Li, Guanglin
AU - Köllner, Tobias G.
AU - Fu, Jianyu
AU - Chen, Xinlu
AU - Xiong, Wangdan
AU - Crandall-Stotler, Barbara J.
AU - Bowman, John L.
AU - Weston, David J.
AU - Zhang, Yong
AU - Chen, Li
AU - Xie, Yinlong
AU - Li, Fay Wei
AU - Rothfels, Carl J.
AU - Larsson, Anders
AU - Graham, Sean W.
AU - Stevenson, Dennis W.
AU - Wong, Gane Ka Shu
AU - Gershenzon, Jonathan
AU - Chen, Feng
PY - 2016/10/25
Y1 - 2016/10/25
N2 - The vast abundance of terpene natural products in nature is due to enzymes known as terpene synthases (TPSs) that convert acyclic prenyl diphosphate precursors into a multitude of cyclic and acyclic carbon skeletons. Yet the evolution of TPSs is not well understood at higher levels of classification. Microbial TPSs from bacteria and fungi are only distantly related to typical plant TPSs, whereas genes similar to microbial TPS genes have been recently identified in the lycophyte Selaginella moellendorffii. The goal of this study was to investigate the distribution, evolution, and biochemical functions of microbial terpene synthase-like (MTPSL) genes in other plants. By analyzing the transcriptomes of 1,103 plant species ranging from green algae to flowering plants, putative MTPSL genes were identified predominantly from nonseed plants, including liverworts, mosses, hornworts, lycophytes, and monilophytes. Directed searching for MTPSL genes in the sequenced genomes of a wide range of seed plants confirmed their general absence in this group. Among themselves, MTPSL proteins from nonseed plants form four major groups, with two of these more closely related to bacterial TPSs and the other two to fungal TPSs. Two of the four groups contain a canonical aspartate-rich "DDxxD" motif. The third group has a "DDxxxD" motif, and the fourth group has only the first two "DD" conserved in this motif. Upon heterologous expression, representative members from each of the four groups displayed diverse catalytic functions as monoterpene and sesquiterpene synthases, suggesting these are important for terpene formation in nonseed plants.
AB - The vast abundance of terpene natural products in nature is due to enzymes known as terpene synthases (TPSs) that convert acyclic prenyl diphosphate precursors into a multitude of cyclic and acyclic carbon skeletons. Yet the evolution of TPSs is not well understood at higher levels of classification. Microbial TPSs from bacteria and fungi are only distantly related to typical plant TPSs, whereas genes similar to microbial TPS genes have been recently identified in the lycophyte Selaginella moellendorffii. The goal of this study was to investigate the distribution, evolution, and biochemical functions of microbial terpene synthase-like (MTPSL) genes in other plants. By analyzing the transcriptomes of 1,103 plant species ranging from green algae to flowering plants, putative MTPSL genes were identified predominantly from nonseed plants, including liverworts, mosses, hornworts, lycophytes, and monilophytes. Directed searching for MTPSL genes in the sequenced genomes of a wide range of seed plants confirmed their general absence in this group. Among themselves, MTPSL proteins from nonseed plants form four major groups, with two of these more closely related to bacterial TPSs and the other two to fungal TPSs. Two of the four groups contain a canonical aspartate-rich "DDxxD" motif. The third group has a "DDxxxD" motif, and the fourth group has only the first two "DD" conserved in this motif. Upon heterologous expression, representative members from each of the four groups displayed diverse catalytic functions as monoterpene and sesquiterpene synthases, suggesting these are important for terpene formation in nonseed plants.
KW - Gene evolution
KW - Nonseed plant
KW - Specialized metabolism
KW - Terpene synthase
UR - http://www.scopus.com/inward/record.url?scp=84992385081&partnerID=8YFLogxK
U2 - 10.1073/pnas.1607973113
DO - 10.1073/pnas.1607973113
M3 - Article
C2 - 27791023
AN - SCOPUS:84992385081
SN - 0027-8424
VL - 113
SP - 12328
EP - 12333
JO - Proceedings of the National Academy of Sciences of the United States of America
JF - Proceedings of the National Academy of Sciences of the United States of America
IS - 43
ER -