Cycloheptaamylose was converted in four steps into a monosulfonylated, hexadeoxy derivative that, on treatment with pyridoxaminethiol, provided an artificial transaminase with activity similar to that found in the nondeoxygenated analogue. Characterization of the intermediate hexadeoxycycloheptaamylose was facilitated by the use of field-desorption mass spectrometry, which was uniquely able to distinguish between penta-, hexa-, and hepta-deoxycycloheptaamylose. A detailed description of experimental methods for the first time makes this modified binding-site available for general use in the design of enzyme mimics.
No. 2 Wenbo Road, Zhangqiu District, Jinan, Shandong
Qilu Normal University · Genelibs Bioinformatics Lab
750 Shunhua Rd, Jinan
2F, Bldg F, University Science Park
Tel: 0531-88819269
Follow our WeChat subscription account for real-time updates and the latest in medical and biological research.
Business Email
E-mail: [email protected]