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Molecular cloning, expression and characterization of cDNA encoding cis‐prenyltransferases from Hevea brasiliensis

A key factor participating in natural rubber biosynthesis

Kasem Asawatreratanakul

Institute of Multidisciplinary Research for Advanced Materials, Tohoku University, Sendai, Japan

Department of Chemistry, Thaksin University, Songkla, Thailand

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Yuan‐Wei Zhang

Institute of Multidisciplinary Research for Advanced Materials, Tohoku University, Sendai, Japan

Present address: Department of Pharmacology, School of Medicine, Yale University, New Haven, CT, USA.Search for more papers by this author
Dhirayos Wititsuwannakul

Department of Biochemistry, Mahidol University, Bangkok, Thailand

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Rapepun Wititsuwannakul

Department of Biochemistry, Prince of Songkla University, Hat‐Yai, Thailand

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Seiji Takahashi

Institute of Multidisciplinary Research for Advanced Materials, Tohoku University, Sendai, Japan

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Atiya Rattanapittayaporn

Department of Biochemistry, Prince of Songkla University, Hat‐Yai, Thailand

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Tanetoshi Koyama

Institute of Multidisciplinary Research for Advanced Materials, Tohoku University, Sendai, Japan

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First published: 28 November 2003
Cited by: 75
T. Koyama, Institute of Multidisciplinary Research for Advanced Materials, Tohoku University, Katahira 2‐1‐1, Aoba‐ku, Sendai 980–8577, Japan. Fax: + 81 22 217 5620, Tel.: + 81 22 217 5621,
E‐mail: koyama@tagen.tohoku.ac.jp

Enzyme: rubber cis‐polyprenylcistransferase (EC 2.5.1.20).

Note: The nucleotide sequences reported in this paper are available in the DDBJ/GenBank™/EMBL Data Bank under the accession numbers AB061234 and AB064661.

Abstract

Natural rubber from Hevea brasiliensis is a high molecular mass polymer of isoprene units with cis‐configuration. The enzyme responsible for the cis‐1,4‐polymerization of isoprene units has been idengified as a particle‐bound rubber transferase, but no gene encoding this enzyme has been cloned from rubber‐producing plants. By using sequence information from the conserved regions of cis‐prenyl chain elongating enzymes that were cloned recently, we have isolated and characterized cDNAs from H. brasiliensis for a functional factor participating in natural rubber biosynthesis. Sequence analysis revealed that all of the five highly conserved regions among cis‐prenyl chain elongating enzymes were found in the protein sequences of the Hevea cis‐prenyltransferase. Northern blot analysis indicated that the transcript(s) of the Hevea cis‐prenyltransferase were expressed predominantly in the latex as compared with other Hevea tissues examined. In vitro rubber transferase assays using the recombinant gene product overexpressed in Escherichia coli revealed that the enzyme catalyzed the formation of long chain polyprenyl products with approximate sizes of 2 × 103−1 × 104 Da. Moreover, in the presence of washed bottom fraction particles from latex, the rubber transferase activity producing rubber product of high molecular size was increased. These results suggest that the Hevea cis‐prenyltransferase might require certain activation factors in the washed bottom fraction particles for the production of high molecular mass rubber.

Number of times cited: 75

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