Abstract
A plasmid pCAMBIA1301 containing Pleurotus eryngii cellulase gene (PEcbh), under the control of Lentinus edodes glyceraldehyde-3-phosphate dehydrogenase (LEgpd) promoter, was constructed and used as an expression vector. The vector was transformed into the tissue of P. eryngii using Agrobacterium tumefaciens-mediated transformation (ATMT) method and 4 transformants (PET1-4) were obtained. The positive transformants were confirmed by cultivation in media containing hygromycin and by PCR amplification of hygromycin B resistance-LEgpd promoter gene fragment. Unpredicted, cellulase specific activities of the transformants were not higher than those of the wild type. Mushroom cultivation was performed in the laboratory and the results revealed that the average biological efficiency of PET4 was significantly 1.52 times higher than those of the wild type.
Acknowledgements
This work was financially supported by Silpakorn University Research and Development Institute (Grant No. SURDI 54/01/10). U.R. was granted by Science Achievement Scholarship of Thailand from The Thailand Research Fund as a Ph.D. student.
- ATMT
Agrobacterium tumefaciens-mediated transformation
- BE
biological efficiency
- CMC
carboxymethylcellulose
- gus
β-glucuronidase
- hph
hygromycin B resistance
- LEgpd
Lentinus edodes glyceraldehyde-3-phosphate dehydrogenase
- PDA
potato dextrose agar
- PEcbh
Pleurotus eryngii cellulase gene
- PET1-4
Pleurotus eryngii transformant strains 1-4
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© 2017 Institute of Molecular Biology, Slovak Academy of Sciences
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- Zoology
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- Zoology
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