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

FEBS Journal - Tập 270 Số 23 - Trang 4671-4680 - 2003
Kasem Asawatreratanakul1,2, Yuan‐Wei Zhang2,3, Dhirayos Wititsuwannakul4, Rapepun Wititsuwannakul5, Seiji Takahashi2, Atiya Rattanapittayaporn5, Tanetoshi Koyama2
1Department of Chemistry, Thaksin University, Songkla, Thailand
2Institute of Multidisciplinary Research for Advanced Materials, Tohoku University, Sendai, Japan
3Present address: Department of Pharmacology, School of Medicine, Yale University, New Haven, CT, USA.
4Department of Biochemistry, Mahidol University, Bangkok, Thailand
5Department of Biochemistry, Prince of Songkla University, Hat-Yai, Thailand

Tóm tắt

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.

Từ khóa


Tài liệu tham khảo

Backhaus R.A., 1985, Rubber formation in plants, Israel J. Bot., 34, 283

d'Auzac J., 1989, Physiology of Rubber Tree Latex

10.1111/j.1095-8339.1987.tb01045.x

10.1104/pp.89.2.506

10.1016/0031-9422(90)85337-F

10.1016/0031-9422(96)00374-3

10.1016/S0031-9422(96)00837-0

Wititsuwannakul D., 2000, Biopolymer, 151

10.1016/S0021-9258(18)51508-8

10.1111/j.1432-1033.1993.tb18374.x

10.1016/S0031-9422(00)95072-6

10.1104/pp.123.3.1133

10.1042/bj0890565

10.1042/bj1010042

10.1351/pac196714010137

10.1016/S0031-9422(96)00838-2

10.1002/app.11674

10.1016/B978-0-08-091283-7.00037-0

10.1021/cr9600464

10.1271/bbb.63.1671

10.1074/jbc.273.31.19476

Apfel C.M., 1999, Use of genomics to idengify bacterial undecaprenyl pyrophosphate synthase: Cloning, expression, and characterization of the essential uppS gene, J. Bacteriol., 181, 482, 10.1128/JB.181.2.483-492.1999

10.1128/MCB.19.1.471

10.1074/jbc.M002000200

10.1016/S0014-5793(00)01798-1

Dennis M.S., 1989, Purification of a prenyltransferase that elongates cis‐polyisoprene rubber from the latex of Hevea brasiliensis, J. Biol. Chem., 264, 18606

10.1073/pnas.87.5.1787

10.1073/pnas.74.12.5463

10.1093/oxfordjournals.jbchem.a124051

10.1038/227680a0

10.1016/0003-2697(76)90527-3

10.1016/S0076-6879(85)10070-4

10.1093/oxfordjournals.jbchem.a022842

10.1074/jbc.M102057200

10.1039/b108934j

10.1046/j.1365-2443.2001.00438.x

Kato J., 1999, The Escherichia coli homologue of yeast RER2, a key enzyme of dolichol synthesis, is essential for carrier lipid formation in bacterial cell wall synthesis, J. Bacterol., 181, 2733, 10.1128/JB.181.9.2733-2738.1999

10.1073/pnas.071514398

10.1021/bi027236v

Lynen F., 1969, Biochemical problems of rubber synthesis, J. Rubb. Res. Inst Malaya, 21, 389

10.1016/S0031-9422(98)00581-0