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Table 2 Examples for the genetically engineering of T. reesei towards overproduction of a metabolite or interesting molecule

From: Cellulases and beyond: the first 70 years of the enzyme producer Trichoderma reesei

Substance produced

Substrate employed

T. reesei strain background

Genetic alteration

Maximum titer

Reference

Ethylene

Wheat straw, cellulose

T. reesei (viride) TL124

Ethylene forming enzyme of Pseudomonas syringae expressed under the cel7a promoter

1.06 µl h−1 g−1 dry weight

[169]

Ethylene

Wheat straw

QM9414

Ethylene forming enzyme of P. syringae expressed under the cel7a, pgk1 and A. nidulans gpdA promoters

4.012 nl h−1 l−1

[170]

N-acetyl-neuraminic acid

Chitin

QM9414

Expression of codon optimized N-acetyl glucosamine-2-epimerase from Anabaena sp. and N-acetyl neuramininc acid synthase from Campylobacter jejuni under the pki1 and xyn1 promoters

13 µg g−1 mycelium

[171]

Xylitol

Barley straw

QM9414

Deletion of xylitol dehydrogenase, double deletion of xylitol dehydrogenase and l-arabinitol-4-dehydrogenase

13.2 g l−1

[172]

Xylitol

Xylose and glucose

QM9414

Knockdown (antisense RNA) of xylulokinase; deletion of xylitol dehydrogenase, overexpression of d-xylose reductase

3.7 g l−1

[173]

Erythritol

Wheat straw

RUT-C30, QM6a

Erythrose reductase expressed under the pki1 and bxl1 promoters

5 mg l−1

[174]