Karamohamed S, Nyrén P
Department of Biotechnology, Royal Institute of Technology, Stockholm, SE-100 44, Sweden.
Anal Biochem. 1999 Jun 15;271(1):81-5. doi: 10.1006/abio.1999.4130.
A real-time, sensitive, and simple assay for detection and quantification of adenosine triphosphate sulfurylase (ATP:sulfate adenylytransferase, EC 2.7.7.4) activity has been developed. The method is based on detection of ATP generated in the ATP sulfurylase reaction between APS and PPi by the firefly luciferase system. For the Saccharomyces cerevisiae ATP sulfurylase, the concentrations of APS and PPi at the half-maximal rate were found to be about 0.5 and 7 microM, respectively. The assay is sensitive and yields linear response between 0.1 microU and 50 mU. The method can be used for monitoring and quantification of recombinant ATP sulfurylase activity in Escherichia coli lysate, as well as for detection of the activity during different purification procedures.
已开发出一种用于检测和定量腺苷三磷酸硫酸化酶(ATP:硫酸腺苷酰转移酶,EC 2.7.7.4)活性的实时、灵敏且简单的检测方法。该方法基于通过萤火虫荧光素酶系统检测在APS和PPi之间的ATP硫酸化酶反应中产生的ATP。对于酿酒酵母ATP硫酸化酶,发现半最大反应速率时APS和PPi的浓度分别约为0.5和7 microM。该检测方法灵敏,在0.1微单位至50毫单位之间产生线性响应。该方法可用于监测和定量大肠杆菌裂解物中重组ATP硫酸化酶的活性,以及在不同纯化过程中检测该活性。