PEMURNIAN PENISILIN ASILASE DARI BAKTERI BAC-4 DENGAN METODE KROMATOGRAFI AFINITAS HDROFOBIK

ABSTRACT:</b><br> <br /> <br /> BAC-4 is one of the local gram positive bacteria that produce penicillin acylase extracelullar enzyme. <br /> In this research, cells of BAC-4 was propagated in the culture medium containing sucrose with the optimum time for cell har...

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Main Author: Muis, Abdul
Format: Theses
Language:Indonesia
Online Access:https://digilib.itb.ac.id/gdl/view/2794
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Institution: Institut Teknologi Bandung
Language: Indonesia
id id-itb.:2794
spelling id-itb.:27942005-12-06T14:04:41ZPEMURNIAN PENISILIN ASILASE DARI BAKTERI BAC-4 DENGAN METODE KROMATOGRAFI AFINITAS HDROFOBIK Muis, Abdul Indonesia Theses INSTITUT TEKNOLOGI BANDUNG https://digilib.itb.ac.id/gdl/view/2794 ABSTRACT:</b><br> <br /> <br /> BAC-4 is one of the local gram positive bacteria that produce penicillin acylase extracelullar enzyme. <br /> In this research, cells of BAC-4 was propagated in the culture medium containing sucrose with the optimum time for cell harvesting 10 hours after fermentation was began. The centrifugation methode was used for enzyme isolation and then purified by ultrafiltration, dialysis and hydrophobic affinity chromatography.</p> The enzyme activity was determined by PDAB (P-dimethylaminobenzaldehide) and the protein content was determined by Lowry methode, while poly acrylamide gel electroforese was used for determining the homogenity of the enzyme. <br /> The spesific activity for the purified enzyme was 1.052 unit/mg. The optimum pH was pH 7.0; temperature 40°C and incubation time 15 minutes. The kinetic data was KM was 2.53 mg/ml, Vm was 0.176 mcl 6 APA/minutes and K= was 6.20 mg/ml. 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
description ABSTRACT:</b><br> <br /> <br /> BAC-4 is one of the local gram positive bacteria that produce penicillin acylase extracelullar enzyme. <br /> In this research, cells of BAC-4 was propagated in the culture medium containing sucrose with the optimum time for cell harvesting 10 hours after fermentation was began. The centrifugation methode was used for enzyme isolation and then purified by ultrafiltration, dialysis and hydrophobic affinity chromatography.</p> The enzyme activity was determined by PDAB (P-dimethylaminobenzaldehide) and the protein content was determined by Lowry methode, while poly acrylamide gel electroforese was used for determining the homogenity of the enzyme. <br /> The spesific activity for the purified enzyme was 1.052 unit/mg. The optimum pH was pH 7.0; temperature 40°C and incubation time 15 minutes. The kinetic data was KM was 2.53 mg/ml, Vm was 0.176 mcl 6 APA/minutes and K= was 6.20 mg/ml.
format Theses
author Muis, Abdul
spellingShingle Muis, Abdul
PEMURNIAN PENISILIN ASILASE DARI BAKTERI BAC-4 DENGAN METODE KROMATOGRAFI AFINITAS HDROFOBIK
author_facet Muis, Abdul
author_sort Muis, Abdul
title PEMURNIAN PENISILIN ASILASE DARI BAKTERI BAC-4 DENGAN METODE KROMATOGRAFI AFINITAS HDROFOBIK
title_short PEMURNIAN PENISILIN ASILASE DARI BAKTERI BAC-4 DENGAN METODE KROMATOGRAFI AFINITAS HDROFOBIK
title_full PEMURNIAN PENISILIN ASILASE DARI BAKTERI BAC-4 DENGAN METODE KROMATOGRAFI AFINITAS HDROFOBIK
title_fullStr PEMURNIAN PENISILIN ASILASE DARI BAKTERI BAC-4 DENGAN METODE KROMATOGRAFI AFINITAS HDROFOBIK
title_full_unstemmed PEMURNIAN PENISILIN ASILASE DARI BAKTERI BAC-4 DENGAN METODE KROMATOGRAFI AFINITAS HDROFOBIK
title_sort pemurnian penisilin asilase dari bakteri bac-4 dengan metode kromatografi afinitas hdrofobik
url https://digilib.itb.ac.id/gdl/view/2794
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