Overexpression of D-Xylose Reductase (xyl1)‎ Gene and Antisense Inhibition of D-Xylulokinase (xyiH)‎ Gene Increase Xylitol Production in Trichoderma reesei

Abstract EN

T.

reesei is an efficient cellulase producer and biomass degrader.

To improve xylitol production in Trichoderma reesei strains by genetic engineering, two approaches were used in this study.

First, the presumptive D-xylulokinase gene in T.

reesei (xyiH), which has high homology to known fungi D-xylulokinase genes, was silenced by transformation of T.

reesei QM9414 strain with an antisense construct to create strain S6-2-2.

The expression of the xyiH gene in the transformed strain S6-2-2 decreased at the mRNA level, and D-xylulokinase activity decreased after 48 h of incubation.

This led to an increase in xylitol production from undetectable levels in wild-type T.

reesei QM9414 to 8.6 mM in S6-2-2.

The T.

reesei Δxdh is a xylose dehydrogenase knockout strain with increased xylitol production compared to the wild-type T.

reesei QM9414 (22.8 mM versus undetectable).

The copy number of the xylose reductase gene (xyl1) in T.

reesei Δxdh strain was increased by genetic engineering to create a new strain Δ9-5-1.

The Δ9-5-1 strain showed a higher xyl1 expression and a higher yield of xylose reductase, and xylitol production was increased from 22.8 mM to 24.8 mM.

Two novel strains S6-2-2 and Δ9-5-1 are capable of producing higher yields of xylitol.

T.

reesei has great potential in the industrial production of xylitol.