STUDI HOMOLOGI DAERAH TERMINAL-C HASIL TRANSLASI INSCRIPTO BEBERAPA GEN DNA POLIMERASE
DNA polymerase plays an important role in DNA replication process. <br /> Commonly the enzyme has three activities, i.e. 5\'--+3\' polymerase, <br /> 5\'-*3\' exonuclease and 3\'->5\' exonuclease which localized in three <br /> different domai...
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id-itb.:16632004-03-08T10:37:49ZSTUDI HOMOLOGI DAERAH TERMINAL-C HASIL TRANSLASI INSCRIPTO BEBERAPA GEN DNA POLIMERASE MULYONO Kimia Indonesia Theses INSTITUT TEKNOLOGI BANDUNG https://digilib.itb.ac.id/gdl/view/1663 DNA polymerase plays an important role in DNA replication process. <br /> Commonly the enzyme has three activities, i.e. 5\'--+3\' polymerase, <br /> 5\'-*3\' exonuclease and 3\'->5\' exonuclease which localized in three <br /> different domains. Orderly the polymerase activity lies on the Cterminal <br /> domain, followed by 3\'->5\' and 5\'-+3\' exonuclease activity <br /> domain on the N-terminal. Information concerning amino acid <br /> sequences on the C-terminal region is important for structure-function <br /> studies of the polymerase activity. Homology studies on DNA <br /> polymerases from different sources by observed on the sequence of the <br /> terminal amino acids have been conducted. C-terminal region of DNA <br /> polymerases (from GenBank i.e. NCBI) were compared which resulted <br /> in 2 conserved amino acid regions i.e. DPNLQNIP and QVHDELL. <br /> These regions which located on the C-terminal of DNA polymerase <br /> has one gap around 200 amino acids. One set of primer pairs were <br /> designed to amplify DNA fragment on the above region. Twelve out <br /> of fourteen of DNA samples, isolated from different organisms, were <br /> amplified by FP1 and PUR1 primers which resulted in 0.6 kb <br /> fragments. These fragments were cloned on pGEM-T vector using E. <br /> colt JM 109 as it\'s host. Restriction analysis on the recombinant <br /> plasmids suggested that the fragment were succesfully ligated. Further <br /> analysis based on nucleotide sequencing suggested that the fragments <br /> length were between 639 to 645 base pairs. All sequences were in <br /> frame with the published DNA polymerase. Inscripto translation and <br /> amino acids comparison among the fragments indicated that the <br /> sequences were relatively different. However, one out of three acidic <br /> amino acids that presumed has an important role on this region was <br /> very conserved as well. <br /> Comparison of the same region of DNA <br /> polymerases with the published data suggested that the organisms <br /> within a genus has specific pattern of amino acid sequences. text |
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Kimia MULYONO STUDI HOMOLOGI DAERAH TERMINAL-C HASIL TRANSLASI INSCRIPTO BEBERAPA GEN DNA POLIMERASE |
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DNA polymerase plays an important role in DNA replication process. <br />
Commonly the enzyme has three activities, i.e. 5\'--+3\' polymerase, <br />
5\'-*3\' exonuclease and 3\'->5\' exonuclease which localized in three <br />
different domains. Orderly the polymerase activity lies on the Cterminal <br />
domain, followed by 3\'->5\' and 5\'-+3\' exonuclease activity <br />
domain on the N-terminal. Information concerning amino acid <br />
sequences on the C-terminal region is important for structure-function <br />
studies of the polymerase activity. Homology studies on DNA <br />
polymerases from different sources by observed on the sequence of the <br />
terminal amino acids have been conducted. C-terminal region of DNA <br />
polymerases (from GenBank i.e. NCBI) were compared which resulted <br />
in 2 conserved amino acid regions i.e. DPNLQNIP and QVHDELL. <br />
These regions which located on the C-terminal of DNA polymerase <br />
has one gap around 200 amino acids. One set of primer pairs were <br />
designed to amplify DNA fragment on the above region. Twelve out <br />
of fourteen of DNA samples, isolated from different organisms, were <br />
amplified by FP1 and PUR1 primers which resulted in 0.6 kb <br />
fragments. These fragments were cloned on pGEM-T vector using E. <br />
colt JM 109 as it\'s host. Restriction analysis on the recombinant <br />
plasmids suggested that the fragment were succesfully ligated. Further <br />
analysis based on nucleotide sequencing suggested that the fragments <br />
length were between 639 to 645 base pairs. All sequences were in <br />
frame with the published DNA polymerase. Inscripto translation and <br />
amino acids comparison among the fragments indicated that the <br />
sequences were relatively different. However, one out of three acidic <br />
amino acids that presumed has an important role on this region was <br />
very conserved as well. <br />
Comparison of the same region of DNA <br />
polymerases with the published data suggested that the organisms <br />
within a genus has specific pattern of amino acid sequences. |
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Theses |
author |
MULYONO |
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MULYONO |
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MULYONO |
title |
STUDI HOMOLOGI DAERAH TERMINAL-C HASIL TRANSLASI INSCRIPTO BEBERAPA GEN DNA POLIMERASE |
title_short |
STUDI HOMOLOGI DAERAH TERMINAL-C HASIL TRANSLASI INSCRIPTO BEBERAPA GEN DNA POLIMERASE |
title_full |
STUDI HOMOLOGI DAERAH TERMINAL-C HASIL TRANSLASI INSCRIPTO BEBERAPA GEN DNA POLIMERASE |
title_fullStr |
STUDI HOMOLOGI DAERAH TERMINAL-C HASIL TRANSLASI INSCRIPTO BEBERAPA GEN DNA POLIMERASE |
title_full_unstemmed |
STUDI HOMOLOGI DAERAH TERMINAL-C HASIL TRANSLASI INSCRIPTO BEBERAPA GEN DNA POLIMERASE |
title_sort |
studi homologi daerah terminal-c hasil translasi inscripto beberapa gen dna polimerase |
url |
https://digilib.itb.ac.id/gdl/view/1663 |
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