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Molecular and physiological studies of nitrate and sulfate uptake in roots of barley Vidmar, Joseph John
Abstract
Molecular and physiological approaches were employed to characterize nitrate and sulfate
transporters from roots of Hordeum vulgare cv. Klondike. A cDNA, hvstl (accession no.
U52867), by heterologous complementation in E. coli. This cDNA encodes a high-affinity sulfate
transporter, that is 2442 bp in length and encodes a protein of 660 amino acids. Under steadystate
conditions of sulfate supply, ranging from 2.5 to 250 μM, sulfate influx (measured at 100
uM external sulfate concentration) and hvst1 transcript levels were inversely correlated with
sulfate concentrations in the culture solution. A time-course study, designed to investigate effects
of S-withdrawal on the abundance of hvst1 transcript, showed a 5-fold increase of the latter
within the first two hours after removing external sulfate, followed by a further slight increase
during the period up to 48 h. These changes were accompanied by a parallel increase in sulfate
influx and a decrease of root glutathione concentrations. When plants that had been deprived of
sulfate for 24 h were exposed to 1 mM L-cysteine, or glutathione, for a period of 3 h, glutathione
was the more effective down regulator of hvstl transcript levels, reducing the latter to a level that
was below that of unstarved controls. Both hvstl transcript abundance and sulfate influx
increased as a function of N-supply to N-starved plants.
Two new cDNAs, bch3 and bch4 (homologous with an Aspergillus nidulans gene
encoding a nitrate transporter, crnA) were isolated from barley roots by RACE PCR. Bch3 and
bch4 are 1822 and 1705 bp, encode putative polypeptides of 507 amino acids, with a predicted
m.w. of 54.6 kDa. Predicted BCH3 and BCH4 proteins are members of a nitrate/nitrite
transporter subfamily of the major facilitator superfamily. Northern blot analysis, revealed that
supplying NO3" to N-deprived plants increased both the abundance of bch transcripts and NO3"
influx. All four bch genes (bch1, bch2, bch3, bch4) are co-ordinately up-regulated in response to
NO3⁻ treatment. Plants provided with 50 pM NO3⁻ showed the highest bch transcript abundance
and , JN03⁻ influx. The effects of exogenous provision of various amino acids on bch transcript
levels was investigated, when plants were co-supplied with nitrate. Asparagine, aspartate,
glutamate and glutamine decreased transcript levels by >60% and ¹³NO₃ influx by 50-80%.
Analysis of amino acid concentrations of roots showed that the decrease of bch transcript was
correlated with increased glutamine levels.
Item Metadata
| Title |
Molecular and physiological studies of nitrate and sulfate uptake in roots of barley
|
| Creator | |
| Publisher |
University of British Columbia
|
| Date Issued |
1999
|
| Description |
Molecular and physiological approaches were employed to characterize nitrate and sulfate
transporters from roots of Hordeum vulgare cv. Klondike. A cDNA, hvstl (accession no.
U52867), by heterologous complementation in E. coli. This cDNA encodes a high-affinity sulfate
transporter, that is 2442 bp in length and encodes a protein of 660 amino acids. Under steadystate
conditions of sulfate supply, ranging from 2.5 to 250 μM, sulfate influx (measured at 100
uM external sulfate concentration) and hvst1 transcript levels were inversely correlated with
sulfate concentrations in the culture solution. A time-course study, designed to investigate effects
of S-withdrawal on the abundance of hvst1 transcript, showed a 5-fold increase of the latter
within the first two hours after removing external sulfate, followed by a further slight increase
during the period up to 48 h. These changes were accompanied by a parallel increase in sulfate
influx and a decrease of root glutathione concentrations. When plants that had been deprived of
sulfate for 24 h were exposed to 1 mM L-cysteine, or glutathione, for a period of 3 h, glutathione
was the more effective down regulator of hvstl transcript levels, reducing the latter to a level that
was below that of unstarved controls. Both hvstl transcript abundance and sulfate influx
increased as a function of N-supply to N-starved plants.
Two new cDNAs, bch3 and bch4 (homologous with an Aspergillus nidulans gene
encoding a nitrate transporter, crnA) were isolated from barley roots by RACE PCR. Bch3 and
bch4 are 1822 and 1705 bp, encode putative polypeptides of 507 amino acids, with a predicted
m.w. of 54.6 kDa. Predicted BCH3 and BCH4 proteins are members of a nitrate/nitrite
transporter subfamily of the major facilitator superfamily. Northern blot analysis, revealed that
supplying NO3" to N-deprived plants increased both the abundance of bch transcripts and NO3"
influx. All four bch genes (bch1, bch2, bch3, bch4) are co-ordinately up-regulated in response to
NO3⁻ treatment. Plants provided with 50 pM NO3⁻ showed the highest bch transcript abundance
and , JN03⁻ influx. The effects of exogenous provision of various amino acids on bch transcript
levels was investigated, when plants were co-supplied with nitrate. Asparagine, aspartate,
glutamate and glutamine decreased transcript levels by >60% and ¹³NO₃ influx by 50-80%.
Analysis of amino acid concentrations of roots showed that the decrease of bch transcript was
correlated with increased glutamine levels.
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| Extent |
11504849 bytes
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| Genre | |
| Type | |
| File Format |
application/pdf
|
| Language |
eng
|
| Date Available |
2009-07-03
|
| Provider |
Vancouver : University of British Columbia Library
|
| Rights |
For non-commercial purposes only, such as research, private study and education. Additional conditions apply, see Terms of Use https://open.library.ubc.ca/terms_of_use.
|
| DOI |
10.14288/1.0099450
|
| URI | |
| Degree (Theses) | |
| Program (Theses) | |
| Affiliation | |
| Degree Grantor |
University of British Columbia
|
| Graduation Date |
1999-11
|
| Campus | |
| Scholarly Level |
Graduate
|
| Aggregated Source Repository |
DSpace
|
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Rights
For non-commercial purposes only, such as research, private study and education. Additional conditions apply, see Terms of Use https://open.library.ubc.ca/terms_of_use.