Preiss J, Crawford K, Downey J, Lammel C, Greenberg E
J Bacteriol. 1976 Jul;127(1):193-203. doi: 10.1128/jb.127.1.193-203.1976.
The regulatory properties of partially purified adenosine 5'-diphosphate-(ADP) glucose pyrophosphorylase from two Serratia marcescens strains (ATCC 274 and ATCC 15365) have been studied. Slight or negligible activation by fructose-P2, pyridoxal-phosphate, or reduced nicotinamide adenine dinucleotide phosphate (NADPH) was observed. These compounds were previously shown to be potent activators of the ADPglucose pyrophosphorylases from the enterics, Salmonella typhimurium, Enterobacter aerogenes, Enterobacter cloacae, Citrobacter freundii, Escherichia aurescens, Shigella dysenteriae, and Escherichia coli. Phosphoenolpyruvate stimulated the rate of ADPglucose synthesis catalyzed by Serratia ADPglucose pyrophosphorylase about 1.5- to 2-fold but did not affect the S0.5 values (concentration of substrate required for 50% maximal stimulation) of the substrates, alpha-glucose-1-phosphate, and adenosine 5'-triphosphate. Adenosine 5'-monophosphate (AMP), a potent inhibitor of the enteric ADPglucose pyrophosphorylase, is an effective inhibitor of the S. marcescens enzyme. ADP also inhibits but is not as effective as AMP. Activators of the enteric enzyme counteract the inhibition caused by AMP. This is in contrast to what is observed for the S. marcescens enzyme. Neither phosphoenolpyruvate, fructose-diphosphate, pyridoxal-phosphate, NADPH, 3-phosphoglycerate, fructose-6-phosphate, nor pyruvate effect the inhibition caused by AMP. The properties of the S. marcescens HY strain and Serratia liquefaciens ADPglucose pyrophosphorylase were found to be similar to the above two S. marcescens enzymes with respect to activation and inhibition. These observations provide another example where the properties of an enzyme found in the genus Serratia have been found to be different from the properties of the same enzyme present in the enteric genera Escherichia, Salmonella, Shigella, Citrobacter, and Enterobacter.
对两种粘质沙雷氏菌菌株(ATCC 274和ATCC 15365)中部分纯化的5'-二磷酸腺苷-(ADP)葡萄糖焦磷酸化酶的调节特性进行了研究。观察到果糖-P2、磷酸吡哆醛或还原型烟酰胺腺嘌呤二核苷酸磷酸(NADPH)的激活作用轻微或可忽略不计。这些化合物先前已被证明是来自肠道菌、鼠伤寒沙门氏菌、产气肠杆菌、阴沟肠杆菌、弗氏柠檬酸杆菌、金黄色埃希氏菌、痢疾志贺氏菌和大肠杆菌的ADP葡萄糖焦磷酸化酶的有效激活剂。磷酸烯醇丙酮酸刺激粘质沙雷氏菌ADP葡萄糖焦磷酸化酶催化的ADP葡萄糖合成速率约1.5至2倍,但不影响底物α-葡萄糖-1-磷酸和5'-三磷酸腺苷的S0.5值(达到最大刺激50%所需的底物浓度)。5'-单磷酸腺苷(AMP)是肠道ADP葡萄糖焦磷酸化酶的有效抑制剂,是粘质沙雷氏菌该酶的有效抑制剂。ADP也有抑制作用,但不如AMP有效。肠道酶的激活剂可抵消AMP引起的抑制作用。这与粘质沙雷氏菌酶的情况相反。磷酸烯醇丙酮酸、二磷酸果糖、磷酸吡哆醛、NADPH、3-磷酸甘油酸、6-磷酸果糖或丙酮酸均不影响AMP引起的抑制作用。发现粘质沙雷氏菌HY菌株和液化沙雷氏菌ADP葡萄糖焦磷酸化酶在激活和抑制方面的特性与上述两种粘质沙雷氏菌酶相似。这些观察结果提供了另一个例子,即发现粘质沙雷氏菌属中一种酶的特性与存在于肠道菌属埃希氏菌、沙门氏菌、志贺氏菌、柠檬酸杆菌和肠杆菌中的同一种酶的特性不同。