Preparation method and application of Trichoderma reesei strain capable of highly yielding penicillium janczewskii Zaleski alpha-galactosidase
A technology of galactosidase and Penicillium yankii, applied in the biological field, can solve the problems of hidden dangers in biological safety, not reaching the level of industrial production, cumbersome procedures, etc., and achieve simple fermentation process, cost reduction, and cheap and easy-to-obtain raw materials. Effect
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[0046] Example 1, Preparation of Trichoderma reesei strain with high yield of Penicillium yanchii α-galactosidase
[0047] 1. Preparation of Trichoderma reesei strain with high production of Penicillium yanchii α-galactosidase
[0048] 1. Construction of Penicillium yanchii α-galactosidase expression vector
[0049] (1) Amplification of Penicillium yanchii α-galactosidase gene
[0050] Using the plasmid containing the full sequence of Penicillium yanchii α-galactosidase gene as a template, PCR amplification was carried out using Pagl-F and Pagl-R primers, and the PCR amplification product was obtained, which was the DNA molecule shown in sequence 1 in the sequence listing , which is the gene fragment of Penicillium yanchii α-galactosidase without signal peptide. The primer sequence is as follows (the underline represents the restriction restriction point): Pagl-F: 5'-G GAATTC CAGGACTCAAACGCAAACCCAATCGTG-3'; Pagl-R:5'-G ACTAGT CTAATGATGATGATGATGATGCTGCCTCTCCCAACATCACAA-3'...
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