Cloning And Expression Of Alkaline Protease Gene From Bacillus Stearothermophilus Strain Fl
Cloning of alkaline protease gene from a thermophilic bacteria, Bacillus stearothermophilus Fl (BSF1) was done by PCR cloning method. Genomic DNA of BSFI was extracted and the highest concentration obtained was 0.46 ug/uL and with a purity of 2.0. Three sets of primers were used including RM5 (5&...
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2000
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my-upm-ir.114362024-06-19T07:26:35Z Cloning And Expression Of Alkaline Protease Gene From Bacillus Stearothermophilus Strain Fl 2000-06 Ab.Hamid, Suhaili Cloning of alkaline protease gene from a thermophilic bacteria, Bacillus stearothermophilus Fl (BSF1) was done by PCR cloning method. Genomic DNA of BSFI was extracted and the highest concentration obtained was 0.46 ug/uL and with a purity of 2.0. Three sets of primers were used including RM5 (5'-CA(CT) GG(ACGT) ACC AA(CT) GTG GC(CGT) GG-3) and RM6 (5'-(ACG)GG GGT (ACG)GC CAT GGA (CGT)CC-3', F0R900 (5-GCA TGC TAC GAT TAA ATA TC-3) and REV900 (5'-CGG CAA TAT CAC ITA GAG TAC C-3') and FOR900 (5'-GCA TGC TAC GAT TAA ATA TC-3') and REV1 591 (5-TGC AGC AGA AAG AAG GAA-3') which resuhed in amplification of 500-bp, 900-bp and 1 500- bp products, respectively. Southern blotting analysis suggested that both 500-bp and 900-bp fragment were present within the 1 500-bp fragment. E. coli TOPIOF Molecular cloning 2000-06 Thesis http://psasir.upm.edu.my/id/eprint/11436/ http://psasir.upm.edu.my/id/eprint/11436/1/FSAS_2000_25.pdf text en public masters Universiti Putra Malaysia Molecular cloning Faculty of Environmental studies Ab. Razak, Nyonya English |
institution |
Universiti Putra Malaysia |
collection |
PSAS Institutional Repository |
language |
English English |
advisor |
Ab. Razak, Nyonya |
topic |
Molecular cloning |
spellingShingle |
Molecular cloning Ab.Hamid, Suhaili Cloning And Expression Of Alkaline Protease Gene From Bacillus Stearothermophilus Strain Fl |
description |
Cloning of alkaline protease gene from a thermophilic bacteria, Bacillus
stearothermophilus Fl (BSF1) was done by PCR cloning method. Genomic DNA
of BSFI was extracted and the highest concentration obtained was 0.46 ug/uL and
with a purity of 2.0. Three sets of primers were used including RM5 (5'-CA(CT)
GG(ACGT) ACC AA(CT) GTG GC(CGT) GG-3) and RM6 (5'-(ACG)GG GGT
(ACG)GC CAT GGA (CGT)CC-3', F0R900 (5-GCA TGC TAC GAT TAA ATA
TC-3) and REV900 (5'-CGG CAA TAT CAC ITA GAG TAC C-3') and FOR900
(5'-GCA TGC TAC GAT TAA ATA TC-3') and REV1 591 (5-TGC AGC AGA
AAG AAG GAA-3') which resuhed in amplification of 500-bp, 900-bp and 1 500-
bp products, respectively. Southern blotting analysis suggested that both 500-bp
and 900-bp fragment were present within the 1 500-bp fragment. E. coli TOPIOF |
format |
Thesis |
qualification_level |
Master's degree |
author |
Ab.Hamid, Suhaili |
author_facet |
Ab.Hamid, Suhaili |
author_sort |
Ab.Hamid, Suhaili |
title |
Cloning And Expression Of Alkaline Protease Gene From Bacillus Stearothermophilus Strain Fl |
title_short |
Cloning And Expression Of Alkaline Protease Gene From Bacillus Stearothermophilus Strain Fl |
title_full |
Cloning And Expression Of Alkaline Protease Gene From Bacillus Stearothermophilus Strain Fl |
title_fullStr |
Cloning And Expression Of Alkaline Protease Gene From Bacillus Stearothermophilus Strain Fl |
title_full_unstemmed |
Cloning And Expression Of Alkaline Protease Gene From Bacillus Stearothermophilus Strain Fl |
title_sort |
cloning and expression of alkaline protease gene from bacillus stearothermophilus strain fl |
granting_institution |
Universiti Putra Malaysia |
granting_department |
Faculty of Environmental studies |
publishDate |
2000 |
url |
http://psasir.upm.edu.my/id/eprint/11436/1/FSAS_2000_25.pdf |
_version_ |
1804888638421467136 |