TRANSFORMASI SACCHAROMYCES CEREVISIAE DENGAN PLASMID YEP-SECRETEX-BGL1 PEMBAWA GEN β-GLOKOSIDASE TRICHODERMA REESEI

Bioethanol produced from cellulose-based material is a promising alternative biofuel. Production of biofuel from cellulose involves two steps, namely conversion of cellulose by enzyme or chemical treatment, and then followed by fermentation of glucose into ethanol by yeast or bacterium. Saccharomyce...

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Main Author: F.A.M. Sinay, Marcell
Format: Final Project
Language:Indonesia
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Online Access:https://digilib.itb.ac.id/gdl/view/71913
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Institution: Institut Teknologi Bandung
Language: Indonesia
id id-itb.:71913
spelling id-itb.:719132023-02-28T09:10:48ZTRANSFORMASI SACCHAROMYCES CEREVISIAE DENGAN PLASMID YEP-SECRETEX-BGL1 PEMBAWA GEN β-GLOKOSIDASE TRICHODERMA REESEI F.A.M. Sinay, Marcell Kimia Indonesia Final Project ß-Glukosidase, Saccharomyces cerevisiae, cellulose INSTITUT TEKNOLOGI BANDUNG https://digilib.itb.ac.id/gdl/view/71913 Bioethanol produced from cellulose-based material is a promising alternative biofuel. Production of biofuel from cellulose involves two steps, namely conversion of cellulose by enzyme or chemical treatment, and then followed by fermentation of glucose into ethanol by yeast or bacterium. Saccharomyces cerevisiae can be transformed into cellulose utilizing yeast by introduction of genes encoding cellulases system. ß-Glukosidase (BGL) is one of cellulase multienzyme system. It hydrolyzes ß-D-(1,4) glycosidic bond of cellobiose to produce glucose. In this study, Eschericia coli and S. cerevisiae were transformed with an expression vector YEp-Secretex containing gene encoding BGL1 (YEp-BGL1). Recombinant plasmids were isolated and were confirmed by restriction analysis using XbaI and NdeI. Culture supernatant of S. cerevisiae harboring YEp-BGL1 showed ß-glukosidase activity at temperature of 50ºC and pH 7.0. text
institution Institut Teknologi Bandung
building Institut Teknologi Bandung Library
continent Asia
country Indonesia
Indonesia
content_provider Institut Teknologi Bandung
collection Digital ITB
language Indonesia
topic Kimia
spellingShingle Kimia
F.A.M. Sinay, Marcell
TRANSFORMASI SACCHAROMYCES CEREVISIAE DENGAN PLASMID YEP-SECRETEX-BGL1 PEMBAWA GEN β-GLOKOSIDASE TRICHODERMA REESEI
description Bioethanol produced from cellulose-based material is a promising alternative biofuel. Production of biofuel from cellulose involves two steps, namely conversion of cellulose by enzyme or chemical treatment, and then followed by fermentation of glucose into ethanol by yeast or bacterium. Saccharomyces cerevisiae can be transformed into cellulose utilizing yeast by introduction of genes encoding cellulases system. ß-Glukosidase (BGL) is one of cellulase multienzyme system. It hydrolyzes ß-D-(1,4) glycosidic bond of cellobiose to produce glucose. In this study, Eschericia coli and S. cerevisiae were transformed with an expression vector YEp-Secretex containing gene encoding BGL1 (YEp-BGL1). Recombinant plasmids were isolated and were confirmed by restriction analysis using XbaI and NdeI. Culture supernatant of S. cerevisiae harboring YEp-BGL1 showed ß-glukosidase activity at temperature of 50ºC and pH 7.0.
format Final Project
author F.A.M. Sinay, Marcell
author_facet F.A.M. Sinay, Marcell
author_sort F.A.M. Sinay, Marcell
title TRANSFORMASI SACCHAROMYCES CEREVISIAE DENGAN PLASMID YEP-SECRETEX-BGL1 PEMBAWA GEN β-GLOKOSIDASE TRICHODERMA REESEI
title_short TRANSFORMASI SACCHAROMYCES CEREVISIAE DENGAN PLASMID YEP-SECRETEX-BGL1 PEMBAWA GEN β-GLOKOSIDASE TRICHODERMA REESEI
title_full TRANSFORMASI SACCHAROMYCES CEREVISIAE DENGAN PLASMID YEP-SECRETEX-BGL1 PEMBAWA GEN β-GLOKOSIDASE TRICHODERMA REESEI
title_fullStr TRANSFORMASI SACCHAROMYCES CEREVISIAE DENGAN PLASMID YEP-SECRETEX-BGL1 PEMBAWA GEN β-GLOKOSIDASE TRICHODERMA REESEI
title_full_unstemmed TRANSFORMASI SACCHAROMYCES CEREVISIAE DENGAN PLASMID YEP-SECRETEX-BGL1 PEMBAWA GEN β-GLOKOSIDASE TRICHODERMA REESEI
title_sort transformasi saccharomyces cerevisiae dengan plasmid yep-secretex-bgl1 pembawa gen ãŽâ²-glokosidase trichoderma reesei
url https://digilib.itb.ac.id/gdl/view/71913
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