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直接用光标记 [P]UDP-葡萄糖以鉴定棉花纤维海藻糖合酶的一个亚基。

Direct Photolabeling with [P]UDP-Glucose for Identification of a Subunit of Cotton Fiber Callose Synthase.

机构信息

Department of Botany, Institute of Life Sciences, The Hebrew University of Jerusalem, 91904, Israel.

出版信息

Plant Physiol. 1991 Feb;95(2):556-63. doi: 10.1104/pp.95.2.556.

Abstract

We have identified a 52 kilodalton polypeptide as being a likely candidate for the catalytic subunit of the UDP-glucose: (1-->3)-beta-glucan (callose) synthase of developing fibers of Gossypium hirsutum (cotton). Such a polypeptide migrates coincident with callose synthase during glycerol gradient centrifugation in the presence of EDTA, and can be directly photolabeled with the radioactive substrate, alpha-[(32)P]UDP-glucose. Interaction with the labeled probe requires Ca(2+), a specific activator of callose synthase which is known to lower the K(m) of higher plant callose synthases for the substrate UDP-glucose. Using this probe and several other related ones, several other proteins which interact with UDP-glucose were also identified, but none satisfied all of the above criteria for being components of the callose synthase.

摘要

我们已经鉴定出一种 52kDa 的多肽,它可能是棉纤维发育过程中 UDP-葡萄糖:(1-->3)-β-葡聚糖(纤维寡糖)合酶的催化亚基。在 EDTA 存在的甘油梯度离心过程中,这种多肽与纤维寡糖合酶一同迁移,并且可以直接用放射性底物 α-[(32)P]UDP-葡萄糖进行光标记。与标记探针的相互作用需要 Ca(2+),这是纤维寡糖合酶的一种特异性激活剂,已知它降低了高等植物纤维寡糖合酶对底物 UDP-葡萄糖的 Km。使用该探针和其他几个相关探针,还鉴定出了几个与 UDP-葡萄糖相互作用的其他蛋白质,但没有一个符合作为纤维寡糖合酶成分的上述所有标准。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1a6d/1077568/f2ecd67e0e57/plntphys00815-0226-a.jpg

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