Rangaswamy V, Altekar W
Radiation Biology and Biochemistry Division, Bhabha Atomic Research Centre, Bombay, India.
J Bacteriol. 1994 Sep;176(17):5505-12. doi: 10.1128/jb.176.17.5505-5512.1994.
Ketohexokinase (ATP:D-fructose 1-phosphotransferase [EC 2.7.1.3]), detected for the first time in a prokaryote, i.e., the extreme halophile Haloarcula vallismortis, was isolated and characterized from the same archaebacterium. This enzyme was characterized with respect to its molecular mass, amino acid composition, salt dependency, immunological cross-reactivity, and kinetic properties. Gel filtration and sucrose density gradient centrifugation revealed a native molecular mass of 100 kDa for halobacterial ketohexokinase, which is larger than its mammalian counterpart. The enzyme could be labeled by UV irradiation in the presence of [ gamma-32P]ATP, suggesting the involvement of a phosphoenzyme intermediate. Other catalytic features of the enzyme were similar to those of its mammalian counterparts. No antigenic cross-reactivity could be detected between the H. vallismortis ketohexokinase and the ketohexokinases from different rat tissues.
首次在原核生物即嗜盐古菌死海嗜盐碱杆菌中检测到的酮己糖激酶(ATP:D-果糖1-磷酸转移酶[EC 2.7.1.3]),是从同一古细菌中分离并鉴定的。对该酶的分子量、氨基酸组成、盐依赖性、免疫交叉反应性和动力学性质进行了表征。凝胶过滤和蔗糖密度梯度离心显示,嗜盐细菌酮己糖激酶的天然分子量为100 kDa,大于其哺乳动物对应物。在[γ-32P]ATP存在下,该酶可通过紫外线照射进行标记,表明存在磷酸酶中间体。该酶的其他催化特性与其哺乳动物对应物相似。在死海嗜盐碱杆菌酮己糖激酶与来自不同大鼠组织的酮己糖激酶之间未检测到抗原交叉反应。