Title of article :
Enzymatic cyclization of 26- and 27-methylidenesqualene to novel unnatural C31 polyprenoids by squalene:hopene cyclase
Author/Authors :
Tanaka، نويسنده , , Hideya and Noguchi، نويسنده , , Hiroshi and Abe، نويسنده , , Ikuro، نويسنده ,
Issue Information :
هفته نامه با شماره پیاپی سال 2004
Pages :
4
From page :
3093
To page :
3096
Abstract :
Squalene:hopene cyclase (SHC) from Alicyclobacillus acidocaldarius accepted 26-methylidenesqualene (26-MS) and 27-methylidenesqualene (27-MS) as a substrate and converted to novel pentacyclic C31 polyprenoids; a dammarene derivative with a 6.6.6.5+6 ring system and 26-methylidene-hop-22(29)-ene, respectively. The broad substrate specificity of the enzyme provided important information on the structure and function of SHC. Interestingly, 27-MS was also found to be a potent inhibitor of the bacterial SHC (IC50=5 μM), while 26-MS just showed poor enzyme inhibition (IC50=ca. 100 μM).
Keywords :
triterpene synthase , Unnatural natural products , Squalene cyclase
Journal title :
Tetrahedron Letters
Serial Year :
2004
Journal title :
Tetrahedron Letters
Record number :
1841268
Link To Document :
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