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Abstract: <br /> <br /> <br /> <br /> Streptococcus pneumoniae clinical isolate was confirmed using microbiological, biochemical and molecular methods. The isolate showed proper characteristic of S.pneumoniae i.e. belongs to Gram positive, the presence of hemolysis, optoch...

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Main Author: Resmiati (NIM: 107 03 063), Melisa
Format: Final Project
Language:Indonesia
Online Access:https://digilib.itb.ac.id/gdl/view/6452
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Institution: Institut Teknologi Bandung
Language: Indonesia
id id-itb.:6452
spelling id-itb.:64522012-06-18T14:51:14Z#TITLE_ALTERNATIVE# Resmiati (NIM: 107 03 063), Melisa Indonesia Final Project INSTITUT TEKNOLOGI BANDUNG https://digilib.itb.ac.id/gdl/view/6452 Abstract: <br /> <br /> <br /> <br /> Streptococcus pneumoniae clinical isolate was confirmed using microbiological, biochemical and molecular methods. The isolate showed proper characteristic of S.pneumoniae i.e. belongs to Gram positive, the presence of hemolysis, optochin sensitive, but negative for sodium deoxycholate solubility test. The nucleotide sequences of 16S rDNA showed high identity to S. pneumoniae, S. mitis and S. oralis. Determination of serotype was done by amplify partial cpsA-cpsB fragment using primer cpsS1 and cpsA3 in several PCR conditions and compositions; however, PCR did not give any PCR product. Isolation of capsular polysaccharide was successfully done and a hexoamine homolog which is one of capsular polysaccharide component of S. pneumoniae. 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: <br /> <br /> <br /> <br /> Streptococcus pneumoniae clinical isolate was confirmed using microbiological, biochemical and molecular methods. The isolate showed proper characteristic of S.pneumoniae i.e. belongs to Gram positive, the presence of hemolysis, optochin sensitive, but negative for sodium deoxycholate solubility test. The nucleotide sequences of 16S rDNA showed high identity to S. pneumoniae, S. mitis and S. oralis. Determination of serotype was done by amplify partial cpsA-cpsB fragment using primer cpsS1 and cpsA3 in several PCR conditions and compositions; however, PCR did not give any PCR product. Isolation of capsular polysaccharide was successfully done and a hexoamine homolog which is one of capsular polysaccharide component of S. pneumoniae.
format Final Project
author Resmiati (NIM: 107 03 063), Melisa
spellingShingle Resmiati (NIM: 107 03 063), Melisa
#TITLE_ALTERNATIVE#
author_facet Resmiati (NIM: 107 03 063), Melisa
author_sort Resmiati (NIM: 107 03 063), Melisa
title #TITLE_ALTERNATIVE#
title_short #TITLE_ALTERNATIVE#
title_full #TITLE_ALTERNATIVE#
title_fullStr #TITLE_ALTERNATIVE#
title_full_unstemmed #TITLE_ALTERNATIVE#
title_sort #title_alternative#
url https://digilib.itb.ac.id/gdl/view/6452
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