Journal of Biochemistry Advance Access published online on December 5, 2006
Journal of Biochemistry, doi:10.1093/jb/mvm004
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© 2006 The Japanese Biochemical Society
Functional Analysis of Eubacterial ent-Copalyl Diphosphate Synthase and Pimara-9(11),15-diene Synthase with Unique Primary Sequences
1Biotechnology Research Center, Toyama Prefectural University, Toyama 939-0398, Japan, 2Faculty of Applied Bio-science, Tokyo University of Agriculture, Setagaya-ku, 156-8502, Japan
Corresponding author: Biotechnology Research Center, Toyama Prefectural University, Toyama 939-0398, Japan. Tel. +81-766-56-7500; Fax. +81-766-56-2498; E-mail: dairi{at}pu-toyama.ac.jp
| Abstract |
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We have previously cloned a DNA fragment that contained four ORFs and was confirmed to participate in viguiepinol {3-hydroxypimara-9(11),15-diene} biosynthesis by a heterologous expression experiment, from Streptomyces sp. strain KO-3988. Of the four ORFs, ORF2 and ORF4 were confirmed to encode an ent-CDP synthase and a GGDP synthase, respectively, by experiments using recombinant enzymes. In this study, ORF3, that did not show similarities with any other known proteins was expressed in E. coli and used for functional analysis. The purified ORF3 product clearly converted ent-CDP into PMD. Since ORF2 and ORF3 are the first examples of enzymes with these biosynthetic functions from prokaryotes, enzymatic properties of both enzymes were investigated. ORF2 is likely to be a dimer and requires a divalent cation such as Mg2+ and Zn2+ for its activity. The optimum pH and temperature were 5.5 and 35 oC. The Km value was calculated to be 13.7 ± 1.0 µM for GGDP and the kcat value was 3.3 x 10-2/sec. ORF3 is likely to be a monomer and also requires a divalent cation. The optimum pH and temperature were 7.0 and 30 oC. The Km value for ent-CDP was estimated to be 2.6 ± 0.2 µM and the kcat value was 1.4 x 10-3/sec.
Key Words: ent-coplalyl diphosphate synthase, diterpene, isoprenoid cyclase, pimara-9(11), 15-diene synthase, Streptomyces
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