Parsons T F, Preiss J
J Biol Chem. 1978 Nov 10;253(21):7638-45.
[3H]Pyridoxal-P can be covalently incorporated into Escherichia coli B mutant strain AC70R1 ADP-glucose synthase by reduction with NaBH4. Two distinct lysine residues can be modified by the allosteric activator pyridoxal-P. Incorporation of [3H]pyridoxal-P in the presence of substrate ADP-glucose + MgCl2 prevents pyridoxylation of an ADP-glucose-protected site and allows modification of the allosteric activator site. Incorporation of [3H]pyridoxal-P in the presence of the allosteric effector, 1,6-hexanediol-P2, protects against pyridoxylation of the allosteric activator site and allows modification of the ADP-glucose-protected site. The activator site CNBr [3H]pyridoxyl-P peptide was purified to homogeneity in the presence of urea by Sephadex G-50 and CM-cellulose chromatography. The peptide consists of 59 residues, with a molecular weight of 6750. The NH2-terminal of the peptide has a 16-residue sequence overlap with the previously determined NH2-terminal sequence of the native enzyme. The activator site pyridoxyl-P lysine is identified as residue 38 of the native enzyme's NH2 terminus. The ADP-glucose-protected site CNBr [3H]pyridoxyl peptide was purified to homogeneity by Sephadex G-50 and DEAE-cellulose chromatography. The peptide consists of 21 residues, with a molecular weight of 2460. The sequence of this peptide has been elucidated.
[3H]吡哆醛磷酸可通过用硼氢化钠还原而共价结合到大肠杆菌B突变株AC70R1的ADP - 葡萄糖合酶中。变构激活剂吡哆醛磷酸可修饰两个不同的赖氨酸残基。在底物ADP - 葡萄糖 + 氯化镁存在下掺入[3H]吡哆醛磷酸可防止ADP - 葡萄糖保护位点的吡哆醛化,并允许变构激活剂位点的修饰。在变构效应剂1,6 - 己二醇 - P2存在下掺入[3H]吡哆醛磷酸可防止变构激活剂位点的吡哆醛化,并允许ADP - 葡萄糖保护位点的修饰。在尿素存在下,通过Sephadex G - 50和CM - 纤维素色谱法将激活剂位点CNBr [3H]吡哆醛 - P肽纯化至同质。该肽由59个残基组成,分子量为6750。该肽的NH2末端与先前确定的天然酶的NH2末端序列有16个残基的序列重叠。激活剂位点的吡哆醛 - P赖氨酸被鉴定为天然酶NH2末端的第38位残基。通过Sephadex G - 50和DEAE - 纤维素色谱法将ADP - 葡萄糖保护位点CNBr [3H]吡哆醛肽纯化至同质。该肽由21个残基组成,分子量为2460。该肽的序列已被阐明。