β-Glucosidases from the Fungus Trichoderma: An Efficient Cellulase Machinery in Biotechnological Applications

Table 1

Studies on β-glucosidase from different strains of Trichoderma fungus.

S. no.	Trichoderma strain	β-glucosidase	Isolation strategies	References
1	T. citrinoviride	Extracellular; β-Glucosidase	Protein purification, biochemical and proteomic characterization	[28]
2	T. reesei	TrBgl2	Mutational studies involving active site residues of the enzyme	[35]
3	T. reesei QM9414	bgl1	Overexpression of bgl1 from Periconia sp. in T. reesei QM9414 under T. reesei tef1α promoter	[37]
4	Recombinant T. reesei strain, X3AB1	bgl1	Construction of T. reesei strain expressing A. aculeatus bg1 under control of xyn3 promoter	[38]
5	T. reesei	bgl I	Molecular cloning and expression in Pichia pastoris	[39]
6	T. reesei CL847	BGL1	Protein purification and kinetic characterization	[3]
7	T. reesei	β-Glucosidase (cel3a)	Molecular cloning and expression in T. reesei	[40]
8	T. ressei	β-Glucosidase BGLII (Cel1A)	Molecular cloning, expression in E. coli, and characterization	[41]
9	T. harzianum C-4	—	Protein purification and biochemical characterization	[42]
10	T. reesei	BGL2	Molecular cloning and expression in Aspergillus oryzae	[43]
11	T. harzianum strain P1	1,3-β-Glucosidase	Protein purification and characterization	[44]
12	T. reesei QM9414	Aryl-β-D-glucosidase	Protein purification and characterization	[45]
13	T. viride	β-Gluc I	Protein purification and biochemical characterization	[46]
14	T. viride QM9414 mutants	—	Biochemical studies (pH control)	[16]