Biochemical characterization of the Pythium ultimum NAD-GDH and genetic analysis of associated genomic regions in Pythium ultimum and Achlya klebsiana
Investigation of an antisense gene pair previously identified in the oomycete 'Achlya klebsiana' and of a NAD-specific glutamate dehydrogenase (NAD-GDH) and putative heat shock 70 stress response protein gene ('hsp70') in the oomycete 'Pythium ultimum' strain 471 were c...
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ndltd-MANITOBA-oai-mspace.lib.umanitoba.ca-1993-18682014-01-31T03:30:57Z Biochemical characterization of the Pythium ultimum NAD-GDH and genetic analysis of associated genomic regions in Pythium ultimum and Achlya klebsiana Barker, Douglas Shaw Investigation of an antisense gene pair previously identified in the oomycete 'Achlya klebsiana' and of a NAD-specific glutamate dehydrogenase (NAD-GDH) and putative heat shock 70 stress response protein gene ('hsp70') in the oomycete 'Pythium ultimum' strain 471 were conducted. The transcriptionally active nature of the ' A. klebsiana' antisense gene pair in both eukaryotic and prokaryotic host cell lines was confirmed although the specific identities and compositions of the transcripts produced were not. The 'P. ultimum' NAD-GDH in crude cell extracts was characterized, and shown to be similar to the previously characterized NAD-GDH of 'Pythium debaryanum', but less so to the NAD-GDH of 'A. klebsiana'. Biochemical characterization of the NAD-GDH included analyses of enzyme instability at several temperatures (counteracted with high concentrations of glycerol); pH optima of both the reductive and oxidative reactions of NAD-GDH (8.8 and 7.2, respectively); induction by L-glutamate; and allosteric activation(of up to 14 fold) by micromolar concentrations of NADP+. As concentrations of NADP + are increased, Km decreased over 10 fold and Vmax increased over 2 fold with _-ketoglutarate as substrate, while Km decreased 30 fold and Vmax increased 1.3 fold with L-glutamate as substrate. Partial sequencing of the putative ' hsp70' gene showed it to have strong homology to other 'hsp70 ' genes, and also to possess consensus sequences corresponding to transcriptional promoter regions (CCAAT boxes, TATAAT boxes, CTF/NF1 binding sites, heat shock elements) in the putative 5' untranslated region. The gene appears to consist of a single open reading frame, which is almost identical to another putative 'hsp70' gene identified in 'A. klebsiana' approximately 7.8 kb away from the ' hsc70':'nad-gdh' antisense gene pair. 2007-05-18T20:01:33Z 2007-05-18T20:01:33Z 1999-10-01T00:00:00Z http://hdl.handle.net/1993/1868 en_US |
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en_US |
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NDLTD |
description |
Investigation of an antisense gene pair previously identified in the oomycete 'Achlya klebsiana' and of a NAD-specific glutamate dehydrogenase (NAD-GDH) and putative heat shock 70 stress response protein gene ('hsp70') in the oomycete 'Pythium ultimum' strain 471 were conducted. The transcriptionally active nature of the ' A. klebsiana' antisense gene pair in both eukaryotic and prokaryotic host cell lines was confirmed although the specific identities and compositions of the transcripts produced were not. The 'P. ultimum' NAD-GDH in crude cell extracts was characterized, and shown to be similar to the previously characterized NAD-GDH of 'Pythium debaryanum', but less so to the NAD-GDH of 'A. klebsiana'. Biochemical characterization of the NAD-GDH included analyses of enzyme instability at several temperatures (counteracted with high concentrations of glycerol); pH optima of both the reductive and oxidative reactions of NAD-GDH (8.8 and 7.2, respectively); induction by L-glutamate; and allosteric activation(of up to 14 fold) by micromolar concentrations of NADP+. As concentrations of NADP + are increased, Km decreased over 10 fold and Vmax increased over 2 fold with _-ketoglutarate as substrate, while Km decreased 30 fold and Vmax increased 1.3 fold with L-glutamate as substrate. Partial sequencing of the putative ' hsp70' gene showed it to have strong homology to other 'hsp70 ' genes, and also to possess consensus sequences corresponding to transcriptional promoter regions (CCAAT boxes, TATAAT boxes, CTF/NF1 binding sites, heat shock elements) in the putative 5' untranslated region. The gene appears to consist of a single open reading frame, which is almost identical to another putative 'hsp70' gene identified in 'A. klebsiana' approximately 7.8 kb away from the ' hsc70':'nad-gdh' antisense gene pair. |
author |
Barker, Douglas Shaw |
spellingShingle |
Barker, Douglas Shaw Biochemical characterization of the Pythium ultimum NAD-GDH and genetic analysis of associated genomic regions in Pythium ultimum and Achlya klebsiana |
author_facet |
Barker, Douglas Shaw |
author_sort |
Barker, Douglas Shaw |
title |
Biochemical characterization of the Pythium ultimum NAD-GDH and genetic analysis of associated genomic regions in Pythium ultimum and Achlya klebsiana |
title_short |
Biochemical characterization of the Pythium ultimum NAD-GDH and genetic analysis of associated genomic regions in Pythium ultimum and Achlya klebsiana |
title_full |
Biochemical characterization of the Pythium ultimum NAD-GDH and genetic analysis of associated genomic regions in Pythium ultimum and Achlya klebsiana |
title_fullStr |
Biochemical characterization of the Pythium ultimum NAD-GDH and genetic analysis of associated genomic regions in Pythium ultimum and Achlya klebsiana |
title_full_unstemmed |
Biochemical characterization of the Pythium ultimum NAD-GDH and genetic analysis of associated genomic regions in Pythium ultimum and Achlya klebsiana |
title_sort |
biochemical characterization of the pythium ultimum nad-gdh and genetic analysis of associated genomic regions in pythium ultimum and achlya klebsiana |
publishDate |
2007 |
url |
http://hdl.handle.net/1993/1868 |
work_keys_str_mv |
AT barkerdouglasshaw biochemicalcharacterizationofthepythiumultimumnadgdhandgeneticanalysisofassociatedgenomicregionsinpythiumultimumandachlyaklebsiana |
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1716628317906403328 |