Geranylation of benzoic acid derivatives by enzymatic extracts from Piper crassinervium (Piperaceae)

被引:24
|
作者
Lopez, Silvia Noeli [1 ]
Lopes, Adriana Aparecida [1 ]
Batista, Joao Marcos, Jr. [1 ]
Flausino, Otavio, Jr. [1 ]
Bolzani, Vanderlan da Silva [1 ]
Kato, Massuo Jorge [2 ]
Furlan, Maysa [1 ]
机构
[1] Univ Estadual Paulista, UNESP, Dept Quim Organ, Inst Quim,NuBBE Nucleo Bioensaios Biossintese & E, BR-14800900 Araraquara, SP, Brazil
[2] Univ Sao Paulo, Inst Quim, BR-05508000 Sao Paulo, Brazil
基金
巴西圣保罗研究基金会;
关键词
Piper crassinervium; Piperaceae; Biotransformation; Geranylation; TRYPANOCIDAL TETRAHYDROFURAN LIGNANS; LITHOSPERMUM-ERYTHRORHIZON; MOLECULAR DESIGN; NATURAL-PRODUCTS; INHIBITORS; PRENYLTRANSFERASE; PRENYLATION; CHROMENES; ADUNCUM; LEAVES;
D O I
10.1016/j.biortech.2010.01.041
中图分类号
S2 [农业工程];
学科分类号
0828 ;
摘要
The ability to carry out geranylations on aromatic substrates using enzymatic extracts from the leaves of Piper crassinervium (Piperaceae) was evaluated. A literature analysis pointed out its importance as a source of prenylated bioactive molecules. The screening performed on aromatic acceptors (benzoic acids, phenols and phenylpropanoids) including geranyl diphosphate as prenyl donor, showed the biotransformation of the 3,4-dihydroxybenzoic acid by the crude extract, and the p-hydroxybenzoic acid by both the microsomal fraction and the crude extract, after treating leaves with glucose. The analysis of the products allowed the identification of C- and O-geranylated derivatives, and the protease (subtilisin and pepsin) inhibition performed on the O-geranylated compounds showed weak inhibition. Electrophoretic profiles indicated the presence of bands/spots among 56-58 kDa and pI 6-7, which are compatible with prenyltransferases. These findings show that P. crassinervium could be considered as a source of extracts with geranyltransferase activity to perform biotransformations on aromatic substrates. (C) 2010 Elsevier Ltd. All rights reserved.
引用
收藏
页码:4251 / 4260
页数:10
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