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Recombinant squalene synthase. synthesis of cyclopentyl non-head-to-tail triterpenes.


ABSTRACT: Incubation of farnesyl diphosphate with recombinant yeast squalene synthase in the absence of NADPH gives a mixture of triterpene hydrocarbons and alcohols, including botryococcene-like compounds with 1'-3 linkages between the farnesyl units. One of these molecules has an unusual cyclopentane structure similar to those recently reported in plant extracts and lakebed sediments.

SUBMITTER: Pan JJ 

PROVIDER: S-EPMC2777528 | biostudies-literature | 2009 Oct

REPOSITORIES: biostudies-literature

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Recombinant squalene synthase. synthesis of cyclopentyl non-head-to-tail triterpenes.

Pan Jian-Jung JJ   Bugni Tim S TS   Poulter C Dale CD  

The Journal of organic chemistry 20091001 19


Incubation of farnesyl diphosphate with recombinant yeast squalene synthase in the absence of NADPH gives a mixture of triterpene hydrocarbons and alcohols, including botryococcene-like compounds with 1'-3 linkages between the farnesyl units. One of these molecules has an unusual cyclopentane structure similar to those recently reported in plant extracts and lakebed sediments. ...[more]

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