Structure–function studies of ultrahigh molecular weight isoprenes provide key insights into their biosynthesis

Author:

Kajiura HiroyukiORCID,Yoshizawa Takuya,Tokumoto YujiORCID,Suzuki Nobuaki,Takeno Shinya,Takeno Kanokwan Jumtee,Yamashita Takuya,Tanaka Shun-ichi,Kaneko Yoshinobu,Fujiyama Kazuhito,Matsumura HiroyoshiORCID,Nakazawa Yoshihisa

Abstract

AbstractSome plant trans-1,4-prenyltransferases (TPTs) produce ultrahigh molecular weight trans-1,4-polyisoprene (TPI) with a molecular weight of over 1.0 million. Although plant-derived TPI has been utilized in various industries, its biosynthesis and physiological function(s) are unclear. Here, we identified three novel Eucommia ulmoides TPT isoformsEuTPT1, 3, and 5, which synthesized TPI in vitro without other components. Crystal structure analysis of EuTPT3 revealed a dimeric architecture with a central hydrophobic tunnel. Mutation of Cys94 and Ala95 on the central hydrophobic tunnel no longer synthesizd TPI, indicating that Cys94 and Ala95 were essential for forming the dimeric architecture of ultralong-chain TPTs and TPI biosynthesis. A spatiotemporal analysis of the physiological function of TPI in E. ulmoides suggested that it is involved in seed development and maturation. Thus, our analysis provides functional and mechanistic insights into TPI biosynthesis and uncovers biological roles of TPI in plants.

Funder

MEXT | Japan Society for the Promotion of Science

Publisher

Springer Science and Business Media LLC

Subject

General Agricultural and Biological Sciences,General Biochemistry, Genetics and Molecular Biology,Medicine (miscellaneous)

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