Characterisation of a Recombinant Patchoulol Synthase Variant for Biocatalytic Production of Terpenes

被引:35
作者
Frister, Thore
Hartwig, Steffen
Alemdar, Semra
Schnatz, Katharina
Thoens, Laura
Scheper, Thomas
Beutel, Sascha
机构
[1] Hannover, Germany
关键词
Terpene synthase; Sesquiterpenes; Biocatalysis; Patchoulol; Essential oil; DELTA-SELINENE SYNTHASE; SESQUITERPENE SYNTHASES; BACTERIAL EXPRESSION; ESSENTIAL OIL; FUNCTIONAL-CHARACTERIZATION; CDNA ISOLATION; CLONING; ASSAY; L; BIOSYNTHESIS;
D O I
10.1007/s12010-015-1707-y
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
The patchoulol synthase (PTS) is a multi-product sesquiterpene synthases which is the central enzyme for biosynthesis of patchouli essential oil in the patchouli plant. Sesquiterpene synthases catalyse the formation of various complex carbon backbones difficult to approach by organic synthesis. Here, we report the characterisation of a recombinant patchoulol synthase complementary DNA (cDNA) variant (PTS var. 1), exhibiting significant amino acid exchanges compared to the native PTS. The product spectrum using the natural substrate E,E-farnesyl diphosphate (FDP) as well as terpenoid products resulting from conversions employing alternative substrates was analysed by GC-MS. In respect to a potential use as a biocatalyst, important enzymatic parameters such as the optimal reaction conditions, kinetic behaviour and the product selectivity were studied as well. Adjusting the reaction conditions, an increased patchoulol ratio in the recombinant essential oil was achieved. Nevertheless, the ratio remained lower than in plant-derived patchouli oil. As alternative substrates, several prenyl diposphates were accepted and converted in numerous compounds by the PTS var. 1, revealing its great biocatalytic potential.
引用
收藏
页码:2185 / 2201
页数:17
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