PENTALENENE SYNTHASE - PURIFICATION, MOLECULAR-CLONING, SEQUENCING, AND HIGH-LEVEL EXPRESSION IN ESCHERICHIA-COLI OF A TERPENOID CYCLASE FROM STREPTOMYCES UC5319
De. Cane et al., PENTALENENE SYNTHASE - PURIFICATION, MOLECULAR-CLONING, SEQUENCING, AND HIGH-LEVEL EXPRESSION IN ESCHERICHIA-COLI OF A TERPENOID CYCLASE FROM STREPTOMYCES UC5319, Biochemistry, 33(19), 1994, pp. 5846-5857
Pentalenene synthase, which catalyzes the cyclization of farnesyl diph
osphate (1) to the tricyclic sesquiterpene hydrocarbon pentalenene (2)
, was purified from Streptomyces UC5319. A 450-bp hybridization probe,
generated by PCR amplification of genomic DNA using primers based on
N-terminal and internal tryptic peptide sequence data for pentalenene
synthase, was used to screen both plasmid and phage DNA libraries of S
treptomyces genomic DNA, resulting in the isolation and sequencing of
the complete pentalenene synthase gene. PCR was used to insert the pen
talenene synthase gene into the T7 expression vector pLM1. Cloning of
the resulting construct in the expression host Escherichia coli BL21(D
E3) gave transformants that expressed pentalenene synthase as greater
than 10% of soluble protein. The recombinant enzyme has been purified,
and initial physical and kinetic characterization has been performed.
The recombinant enzyme appears to be identical in every respect with
the native Streptomyces synthase and exhibits the following steady-sta
te kinetic parameters: K-m = 0.31 +/- 0.05 mu M, k(cat) = 0.32 +/- 0.0
2 s(-1), K-I(PPi) = 3.2 +/- 0.6 mu M. Both enzymes have an absolute re
quirement of Mg2+ for catalysis and an optimum pH of 8.2-8.4. Both pro
teins have M(r) values of 41-42 kDa, as determined by SDS-PAGE.