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dc.contributor.authorAravind Madhavan-
dc.contributor.authorRajeev K Sukumaran-
dc.date.accessioned2014-08-13T06:35:17Z-
dc.date.available2014-08-13T06:35:17Z-
dc.date.issued2014-
dc.identifier.citationBioresource Technology 165:302-308;Aug 2014en_US
dc.identifier.issn0960-8524-
dc.identifier.urihttp://ir.niist.res.in:8080/jspui/handle/123456789/1625-
dc.description.abstractCross-recognition of promoters from filamentous fungi in yeast can have important consequences towards developing fungal expression systems, especially for the rapid evaluation of their efficacy. A truncated 510 bp inducible Trichoderma reesei cellobiohydrolase I (cbh1) promoter was tested for the expression of green fluorescent protein (GFP) in Kluyveromyces lactis after disrupting its native beta-galactosidase (lac4) promoter. The efficiency of the CBH1 secretion signal was also evaluated by fusing it to the lac4 promoter of the yeast, which significantly increased the secretion of recombinant protein in K. lactis compared to the native a-mating factor secretion signal. The fungal promoter is demonstrated to have potential to drive heterologous protein production in K. lactis; and the small sized T. reesei cbh1 secretion signal can mediate the protein secretion in K. lactis with high efficiency.en_US
dc.language.isoenen_US
dc.publisherElsevieren_US
dc.subjectSecretion signalen_US
dc.subjectCellobiohydrolaseen_US
dc.subjectHeterologous proteinsen_US
dc.subjectKluyveromycesen_US
dc.subjectPromoteren_US
dc.titlePromoter and signal sequence from filamentous fungus can drive recombinant protein production in the yeast Kluyveromyces lactisen_US
dc.typeArticleen_US
Appears in Collections:2014

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