Rothschild A, Wald F A, Bocca S N, Tandecarz J S
Instituto de Investigaciones Bioquímicas Fundación Campomar, I.I.B.B.A., CONICET, Facultad de Ciencias Exactas y Naturales, U.B.A., Argentina.
Cell Mol Biol (Noisy-le-grand). 1996 Jul;42(5):645-51.
UDP-glucose: protein transglucosylase (UPTG, EC 2.4.1.112) catalyzes the first step of protein-bound alpha-glucan synthesis in potato tuber and developing maize endosperm. The presence of a non-dialyzable, heat labile protein responsible for low levels of UPTG activity in developing maize endosperm was investigated. UPTG activity in 5-day old maize seedlings and potato tuber solubilized preparations was also reduced by the endosperm preparation. FPLC-Mono Q column chromatography of developing maize endosperm was effective in separating the inhibitor protein (IP) from UPTG. After gel filtration on Superose 12, IP yielded a major polypeptide of about 80 kDa on SDS-PAGE. IP was purified by gel filtration on Superose 12 and preparative SDS-PAGE, and specific antibodies were prepared. Polyclonal antibodies reacted specifically with an 80 kDa polypeptide of developing maize endosperm on Western blot. They also recognized a similar band in 5-day old maize seedlings, but not in potato tubers. The identification of a factor that regulates the level of UPTG activity in developing maize endosperm may help to elucidate the functional role of the enzyme in the initiation of starch synthesis during seed development.
UDP-葡萄糖:蛋白质转葡糖基酶(UPTG,EC 2.4.1.112)催化马铃薯块茎和发育中的玉米胚乳中蛋白质结合的α-葡聚糖合成的第一步。研究了发育中的玉米胚乳中一种不可透析、热不稳定的蛋白质与低水平UPTG活性的关系。胚乳制剂也降低了5日龄玉米幼苗和马铃薯块茎可溶制剂中的UPTG活性。对发育中的玉米胚乳进行快速蛋白质液相色谱-单Q柱色谱可有效分离抑制蛋白(IP)和UPTG。在Superose 12上进行凝胶过滤后,IP在SDS-PAGE上产生一条约80 kDa的主要多肽。通过在Superose 12上进行凝胶过滤和制备性SDS-PAGE对IP进行纯化,并制备特异性抗体。多克隆抗体在蛋白质免疫印迹中与发育中的玉米胚乳的80 kDa多肽发生特异性反应。它们在5日龄玉米幼苗中也识别出类似条带,但在马铃薯块茎中未识别出。鉴定发育中的玉米胚乳中调节UPTG活性水平的因子可能有助于阐明该酶在种子发育过程中淀粉合成起始中的功能作用。