| Literature DB >> 26242868 |
Yasushi Yonezawa1, Aiko Nagayama, Hiroko Tokunaga, Matsujiro Ishibashi, Shigeki Arai, Ryota Kuroki, Keiichi Watanabe, Tsutomu Arakawa, Masao Tokunaga.
Abstract
Nucleoside diphosphate kinase isolated from psychrophilic Pseudoalteromonas sp. AS-131 (ASNDK) was expressed in Escherichia coli and purified to homogeneity. Comparing to mesophilic NDK isolated from Pseudomonas aeruginosa, ASNDK exhibited highly elevated thermolability: E. coli expression at 37 °C as a denatured insoluble form, 30 °C lower optimum temperature of enzymatic activity, and greatly reduced heat stability with 38 °C lower Tm value, fourfold higher Km and reduced Kcat/Km by 0.4-fold upon reaction temperature increase from 20 to 37 °C. The subunit structure of ASNDK was suggested to be dimer, as in NDKs isolated from moderate halophiles.Entities:
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Year: 2015 PMID: 26242868 DOI: 10.1007/s10930-015-9623-0
Source DB: PubMed Journal: Protein J ISSN: 1572-3887 Impact factor: 2.371