Characterization and complementation of a Pichia stipitis mutant unable to grow on D-xylose or L-arabinose

被引:27
|
作者
Shi, NQ
Prahl, K
Hendrick, J
Cruz, J
Lu, P
Cho, JY
Jones, S
Jeffries, T
机构
[1] US Forest Serv, USDA, Forest Prod Lab, Madison, WI 53705 USA
[2] Univ Wisconsin, Dept Biochem, Madison, WI 53706 USA
[3] Univ Wisconsin, Dept Bacteriol, Madison, WI 53706 USA
关键词
D-Xylose; L-arabinose; Pichia stipitis; fermentation; metabolism; mutant; complementation;
D O I
10.1385/ABAB:84-86:1-9:201
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Pichia stipitis CBS 6054 will grow on D-xylose, D-arabinose, and L-arabinose. D-Xylose and L-arabinose are abundant in seed hulls of maize, and their utilization is important in processing grain residues. To elucidate the degradation pathway for L-arabinose, we obtained a mutant, FPL-MY30, that was unable to grow on D-xylose and L-arabinose but that could grow on D-arabinitol. Activity assays of oxidoreductase and pentulokinase enzymes involved in D-xylose, D-arabinose, and L-arabinose pathways indicated that FPL-MY30 is' deficient in D-xylitol dehydrogenase (D-XDH), D- and L-arabinitol dehydrogenases, and D-ribitol dehydrogenase. Transforming FPL-MY30 with a gene for xylitol dehydrogenase (PsXYL2), which was cloned from CBS 6054 (GenBank AF127801), restored the D-XDH activity and the capacity for FPL-MY30 to grow on L-arabinose. This suggested that FPL-MY30 is critically deficient in XYL2 and that the D-xylose and L-arabinose metabolic pathways have xylitol as a common intermediate. The capacity for FPL-MY30 to grow on D-arabinitol could proceed through D-ribulose.
引用
收藏
页码:201 / 216
页数:16
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