Heterologous Expression of Secondary Metabolite Genes in Trichoderma reesei for Waste Valorization

被引:10
|
作者
Shenouda, Mary L. [1 ,2 ]
Ambilika, Maria [1 ]
Skellam, Elizabeth [1 ,3 ,4 ]
Cox, Russell J. [1 ]
机构
[1] Inst Organ Chem & Biomol Wirkstoffzentrum BMWZ, Schneiderberg 38, D-30167 Hannover, Germany
[2] Alexandria Univ, Fac Pharm, Pharmacognosy Dept, Alexandria 21521, Egypt
[3] Univ North Texas, Dept Chem, 1155 Union Circle, Denton, TX 76201 USA
[4] Univ North Texas, BioDiscovery Inst, 1155 Union Circle, Denton, TX 76201 USA
关键词
heterologous expression; PKS-NRPS; PKS; waste valorization; microbial cell factory; Trichoderma reesei; POLYKETIDE SYNTHASE; TRANSFORMATION SYSTEM; BIOSYNTHESIS; IDENTIFICATION; DIVERSITY; PATHWAY; ACE1;
D O I
10.3390/jof8040355
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Trichoderma reesei (Hypocrea jecorina) was developed as a microbial cell factory for the heterologous expression of fungal secondary metabolites. This was achieved by inactivation of sorbicillinoid biosynthesis and construction of vectors for the rapid cloning and expression of heterologous fungal biosynthetic genes. Two types of megasynth(et)ases were used to test the strain and vectors, namely a non-reducing polyketide synthase (nr-PKS, aspks1) from Acremonium strictum and a hybrid highly-reducing PKS non-ribosomal peptide synthetase (hr-PKS-NRPS, tenS + tenC) from Beauveria bassiana. The resulting engineered T. reesei strains were able to produce the expected natural products 3-methylorcinaldehyde and pretenellin A on waste materials including potato, orange, banana and kiwi peels and barley straw. Developing T. reesei as a heterologous host for secondary metabolite production represents a new method for waste valorization by the direct conversion of waste biomass into secondary metabolites.
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页数:13
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