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DC Field | Value | Language |
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dc.contributor.author | Rajoka, Muhammad I. | - |
dc.contributor.author | Parvez, S. | - |
dc.contributor.author | Malik, Dr. Kauser .A. | - |
dc.date.accessioned | 2021-05-30T15:36:51Z | - |
dc.date.available | 2021-05-30T15:36:51Z | - |
dc.date.issued | 1992-11 | - |
dc.identifier.citation | Rajoka, M.I., Parvez, S. & Malik, K.A. Cloning of structural genes for ß-glucosidase fromCellulomonas biazotea intoE. coli andSaccharomyces cerevisiae using shuttle vector pBLU-D. Biotechnol Lett 14, 1001–1006 (1992). https://doi.org/10.1007/BF01021048 | en_US |
dc.identifier.other | https://doi.org/10.1007/BF01021048 | - |
dc.identifier.uri | http://localhost:8080/xmlui/handle/123456789/1344 | - |
dc.description | https://doi.org/10.1007/BF01021048 | en_US |
dc.description.abstract | A Smal genomic library fromCellulomonas biazotea NIAB 442 was constructed inEscherichia coli HB101 using shuttle vector pBLU-D. Three clones with ability to hydrolyse esculin were isolated. These clones were comparedin vivo andin vitro tests to select for hyper-secretion of ß-glucosidase. The recombinant plasmids were transformed to competent cells of a Ciro yeast.In vivo studies indicated that the genes were fully expressed in yeast as well. | en_US |
dc.language.iso | en | en_US |
dc.publisher | springer link | en_US |
dc.relation.ispartofseries | Biotechnol Lett 14, 1001–1006 (1992).; | - |
dc.subject | cloning | en_US |
dc.subject | structural | en_US |
dc.subject | genes | en_US |
dc.subject | biazotea | en_US |
dc.title | Cloning of structural genes for ß-glucosidase fromCellulomonas biazotea intoE. coli andSaccharomyces cerevisiae using shuttle vector pBLU-D | en_US |
dc.type | Article | en_US |
Appears in Collections: | School of Life Sciences |
Files in This Item:
File | Description | Size | Format | |
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clonning of structural genes for B glucosedase.pdf | 1.68 MB | Adobe PDF | View/Open |
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