Hansen Michael Riis, Tranekjaer Jørgensen Jesper, Dandanell Gert
Department of Biological Chemistry, Institute of Molecular Biology and Physiology, University of Copenhagen, Sølvgade 83 H, 1307 Copenhagen K, Denmark.
J Bacteriol. 2006 Jun;188(11):4153-7. doi: 10.1128/JB.01926-05.
xapABR from Salmonella enterica was analyzed and compared with the corresponding Escherichia coli genes. xapB and xapR, but not xapA, encode functional proteins. An S. enterica XapA(Asp72Gly) mutant that restores the phosphorolytic activity was selected. The purified mutant enzyme has different kinetic constants than the E. coli enzyme but similar substrate specificity.
对来自肠炎沙门氏菌的xapABR进行了分析,并与相应的大肠杆菌基因进行了比较。xapB和xapR编码功能蛋白,而xapA不编码。筛选出了一种恢复磷酸解活性的肠炎沙门氏菌XapA(Asp72Gly)突变体。纯化后的突变酶与大肠杆菌酶具有不同的动力学常数,但底物特异性相似。