Villemez C L, Franz G, Hassid W Z
Department of Biochemistry, University of California, Berkeley, California 94720.
Plant Physiol. 1967 Sep;42(9):1219-23. doi: 10.1104/pp.42.9.1219.
A particulate enzyme system from Phaseolus aureus seedlings catalyzes the synthesis of alkali insoluble polysaccharide material from UDP-d-glucose. 80 to 90% of the d-glucose units are joined by beta-1,4 linkages, the remainder being combined by beta-1,3 linkages. It is not known whether the material is a single polysaccharide or a mixture.With a substrate concentration of 4 x 10(-3)m the enzyme system catalyzes the formation of alkali insoluble polysaccharide from UDP-d-glucose at a rate 23 times greater than that from GDP-d-glucose. The modifications introduced also increase the formation of cellulose from GDP-d-glucose to 3 times the rate previously reported.None of the glycosyl nucleotides containing bases other than guanine or uracil (adenine, cytosine, thymine) served as substrate for the production of alkali insoluble polysaccharide with this enzyme system. dUDP-d-glucose could also not serve as substrate.
来自金甲豆幼苗的一种颗粒酶系统催化由UDP - D -葡萄糖合成碱不溶性多糖物质。80%至90%的D -葡萄糖单元通过β - 1,4键连接,其余部分通过β - 1,3键结合。尚不清楚该物质是单一多糖还是混合物。在底物浓度为4×10⁻³m时,该酶系统催化由UDP - D -葡萄糖形成碱不溶性多糖的速率比由GDP - D -葡萄糖形成的速率高23倍。引入的修饰还将由GDP - D -葡萄糖形成纤维素的速率提高到先前报道速率的3倍。含有除鸟嘌呤或尿嘧啶(腺嘌呤、胞嘧啶、胸腺嘧啶)以外碱基的糖基核苷酸均不能作为该酶系统产生碱不溶性多糖的底物。dUDP - D -葡萄糖也不能作为底物。