DIRECT PHOTOLABELING WITH [P-32] UDP-GLUCOSE FOR IDENTIFICATION OF A SUBUNIT OF COTTON FIBER CALLOSE SYNTHASE

被引:59
作者
DELMER, DP
SOLOMON, M
READ, SM
机构
[1] Department of Botany, Institute of Life Sciences, Hebrew University of Jerusalem
[2] Plant Cell Biology Research Centre, School of Botany, University of Melbourne, Parkville
关键词
D O I
10.1104/pp.95.2.556
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
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-[P-32]UDP-glucose. Interaction with the labeled probe requires Ca2+, 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.
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页码:556 / 563
页数:8
相关论文
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