Department of Bioscience and Biotechnology, Bio/Molecular Informatics Center, Konkuk University, Seoul 143-701, Republic of Korea.
Plant Physiol Biochem. 2009 Nov-Dec;47(11-12):991-7. doi: 10.1016/j.plaphy.2009.08.004. Epub 2009 Aug 27.
In this study, a flavonoid malonyltransferase (OsMaT-2) was cloned from Oryza sativa, and the recombinant protein OsMaT-2 was purified via affinity chromatography. OsMaT-2 utilized a variety of flavonoid glucosides, including flavanone glucosides, flavone glucosides, flavonol glucosides, and isoflavone glucosides as substrates, but did not utilize anthocyanin. As an acyl donor, OsMaT-2 utilized only malonyl-CoA. Based on reactions with various quercetin 3-O-sugars, we identified the probable position of malonylation as the 6''-hydroxyl group of the sugar. This is the first report, to the best of our knowledge, of the cloning of a flavonoid malonyltransferase from O. sativa.
在这项研究中,我们从水稻中克隆了一种类黄酮丙二酰基转移酶(OsMaT-2),并通过亲和层析对重组蛋白 OsMaT-2 进行了纯化。OsMaT-2 可利用多种类黄酮糖苷作为底物,包括黄烷酮糖苷、黄酮糖苷、黄酮醇糖苷和异黄酮糖苷,但不利用花青素。作为酰基供体,OsMaT-2 仅利用丙二酰辅酶 A。基于与各种槲皮素 3-O-糖的反应,我们确定了丙二酰化的可能位置是糖的 6''-羟基。据我们所知,这是首次从水稻中克隆出一种类黄酮丙二酰基转移酶。