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Trichoderma reesei RUT C-30

ABSTRACT: Trichoderma reesei RUT C-30 Genome sequencing and assembly

PROVIDER: PRJNA207855 | ENA |

REPOSITORIES: ENA

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			Action	DRS
	JABP01.dat.gz	Other
	JABP01.fasta.gz	Fasta.gz
	JABP01.master.dat	Other
	SRR3927520_1.fastq.gz	Fastqsanger.gz
	SRR3927520_2.fastq.gz	Fastqsanger.gz

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Project description:Enzyme production by T. reesei Rut C-30 was studied in submerged cultures on five different cellulose-rich substrates, namely, commercial cellulose Avicel® and industrial-like cellulosic pulp substrates which consist mainly of cellulose, but also contain residual hemicellulose and lignin. In order to evaluate the hydrolysis of the substrates by the fungal enzymes, the spatial polymer distributions were characterised by cross-polarization magic angle spinning carbon-13 nuclear magnetic resonance (CP/MAS 13C-NMR) in combination with spectral fitting. Proteins in culture supernatants at early and late stages of enzyme production were labeled by Tandem Mass Tags (TMT) and protein profiles were analysed by liquid chromatography-tandem mass spectrometry.

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ArrayCGH of Trichoderma reesei strains QM9123, QM9414, NG14 and RutC-30

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