Molecular cloning and characterization of two YGL039w genes encoding broad specificity NADPH-dependent aldehyde reductases from Kluyveromyces marxianus strain DMB1

作者：Akita Hironaga^*; Watanabe Masahiro; Suzuki Toshihiro; Nakashima Nobutaka; Hoshino Tamotsu

来源：FEMS Microbiology Letters, 2015, 362(16): fnv116.

DOI：10.1093/femsle/fnv116

• aldehyde inhibitor
• Kluyveromyces marxianus
• methylglyoxal
• reductase

Two genes from Kluyveromyces marxianus strain DMB1, YGL039w1 and YGL039w2, encode putative uncharacterized oxidoreductases that respectively share 42 and 44% identity with the Saccharomyces cerevisiae S288c NADPH-dependent methylglyoxal reductase (EC 1.1.1.283). To determine the enzymatic characteristics of their products, the two genes were expressed in recombinant Escherichia coli cells, after which the YGL039w1 and YGL039w2 proteins were purified to homogeneity. In the presence of NADPH, both enzymes showed reductive activities toward at least nine aldehyde substrates, but no NADP(+)-dependent oxidative activities. These two YGL039w proteins thus appear to be aldehyde reductases. In addition, although both enzymes retained more than 70% of their activities after incubation for 30 min at temperatures below 40 degrees C or at pHs between 5.5 and 11.3, YGL039w2 was slightly more thermostable than YGL039w1.

• 出版日期2015-8