Goldberg D E, Rumley M K, Kennedy E P
Proc Natl Acad Sci U S A. 1981 Sep;78(9):5513-7. doi: 10.1073/pnas.78.9.5513.
Membrane-derived oligosaccharides (MDO) are glucose-containing constituents of the periplasmic space of Escherichia coli whose biosynthesis is closely linked to the metabolism of membrane phospholipids. A periplasmic enzyme has now been discovered that catalyzes the transfer of phosphoglycerol residues between species of MDO or to certain glucose-containing model substrates such as gentiobiose (6-O-beta-D-glucopyranosyl-D-glucose). The partially purified enzyme has an apparent molecular weight of about 56,000 in gel permeation chromatography, and has an absolute requirement for divalent cations, of which Mn2+ is most active. Although the transferase activity appears to be the physiological function of the enzyme, at low concentrations of acceptor, the enzyme (Enz) acts as a cyclase, with the liberation of cyclic 1(3),2-phosphoglycerol, suggesting the following mechanism: (formula, see text).
膜衍生寡糖(MDO)是大肠杆菌周质空间中含葡萄糖的成分,其生物合成与膜磷脂的代谢密切相关。现已发现一种周质酶,它催化MDO不同种类之间或向某些含葡萄糖的模型底物(如龙胆二糖(6-O-β-D-吡喃葡萄糖基-D-葡萄糖))转移磷酸甘油残基。在凝胶渗透色谱中,部分纯化的酶的表观分子量约为56,000,并且对二价阳离子有绝对需求,其中Mn2+活性最高。尽管转移酶活性似乎是该酶的生理功能,但在低浓度受体时,该酶(Enz)作为环化酶起作用,释放出环状1(3),2-磷酸甘油,提示以下机制:(公式,见原文)。