Tronick S R, Ciardi J E, Stadtman E R
J Bacteriol. 1973 Sep;115(3):858-68. doi: 10.1128/jb.115.3.858-868.1973.
Antisera prepared against adenylylated and unadenylylated Escherichia coli glutamine synthetase cross-reacted with the glutamine synthetases from a number of gram-negative bacteria and one gram-variable species as demonstrated by immunodiffusion and inhibition of enzyme activity. In contrast, the antisera did not cross-react with the glutamine synthetases from gram-positive bacteria (with one exception) nor with the synthetases of higher organisms. Modification of the various glutamine synthetases by covalent attachment of adenosine 5'-monophosphate (or other nucleotides) was tested for by determining whether or not snake venom phosphodiesterase altered catalytic activity in a manner similar to its effect on adenylylated E. coli glutamine synthetase. Only the activity of the glutamine synthetases from gram-negative bacteria grown with specific levels of nitrogen sources could be altered by snake venom phosphodiesterase. In addition, a relative order of antigenic homology between cross-reacting enzymes was suggested based on the patterns of spur formation in the immunodiffusion assay.
通过免疫扩散和酶活性抑制试验表明,针对腺苷酸化和未腺苷酸化的大肠杆菌谷氨酰胺合成酶制备的抗血清,能与多种革兰氏阴性菌及一种革兰氏可变菌的谷氨酰胺合成酶发生交叉反应。相比之下,该抗血清与革兰氏阳性菌(有一个例外)的谷氨酰胺合成酶以及高等生物的合成酶均无交叉反应。通过测定蛇毒磷酸二酯酶是否能以类似于其对腺苷酸化大肠杆菌谷氨酰胺合成酶的作用方式改变催化活性,来检测通过共价连接5'-单磷酸腺苷(或其他核苷酸)对各种谷氨酰胺合成酶进行的修饰。只有在特定氮源水平下生长的革兰氏阴性菌的谷氨酰胺合成酶活性能被蛇毒磷酸二酯酶改变。此外,基于免疫扩散试验中刺突形成的模式,提出了交叉反应酶之间抗原同源性的相对顺序。