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  • 1
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Science Ltd
    Plant, cell & environment 27 (2004), S. 0 
    ISSN: 1365-3040
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology
    Notes: The relative abundances of key gene transcripts encoding proteins involved in inducible inorganic carbon (Ci) transport in the cyanobacterium Synechocystis PCC6803 were quantified by real-time reverse-transcriptase-polymerase chain reaction under conditions of varying Ci and light levels. Significant increases in CO2-concentrating mechanism (CCM)-related transcript abundance were observed only in cells aerated with CO2-free air for 30 min in the light, but not in the dark, relative to illuminated cells grown at high CO2 levels (high-Ci cells). Cells were incubated under precisely defined conditions in a cuvette attached to a mass spectrometer to allow for the measurement of photosynthetic gas exchange rates, [Ci] and [O2], in combination with quantitative analysis of transcripts. Under conditions of increasing irradiance and low [Ci], or under conditions of decreasing [Ci] at constant irradiance, the abundances of cmpA (encoding part of the BCT1 HCO3– transporter), ndhF3 (encoding subunit of high-affinity CO2 uptake system) and sbtA (encoding Na+-dependent HCO3– transporter) transcripts tended to increase, relative to illuminated cells grown at high-CO2. The cmpA transcript appeared to be less responsive to decreasing [Ci] than either ndhF3 or sbtA. The induction of cmpA and ndhF3 transcripts was completely inhibited by 10 µm 3-(3,4-dichlorophenyl)-1,1-dimethylurea (DCMU) compared to untreated control cells. This inhibitor had no effect on sbtA expression. In the presence of 2,6-dichlorobenzoquinone (DCBQ), the expression of the cmpA transcript tracked the apparent rate of O2 evolution from photosystem II closely as the irradiance was increased, reaching maximum levels of expression approximately 16-fold higher than control cells. Under the same conditions, the ndhF3 transcript increased by two- to three-fold, whereas the sbtA transcript did not respond to this treatment. The regulation of CCM induction in this strain is discussed in relation to current hypotheses on the sensing of Ci limitation.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Science Ltd
    Plant, cell & environment 27 (2004), S. 0 
    ISSN: 1365-3040
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology
    Notes: Carbonic anhydrase (CA, EC 4.2.1.1) catalyses the first reaction in the C4 photosynthetic pathway, the conversion of atmospheric CO2 to bicarbonate in the mesophyll cytosol. To examine the importance of the enzyme to the functioning of the C4 photosynthetic pathway, Flaveria bidentis (L.) Kuntze, a C4 dicot, was genetically transformed with an antisense construct in which the cDNA encoding a putative cytosolic CA (CA3) was placed under the control of a constitutive promoter. Some of the primary transformants had impaired CO2 assimilation rates and required high CO2 for growth. The T1 progeny of four primary transformants were used to examine the quantitative relationship between leaf CA activity and CO2 assimilation rate. CA activity was determined in leaf extracts with a mass spectrometric technique that measured the rate of 18O exchange from doubly labelled 13C18O2. Steady-state CO2 assimilation rates were unaffected by a decrease in CA activity until CA activity was less than 20% of wild type when they decreased steeply. Transformants with less than 10% of wild-type CA activity had very low CO2 assimilation rates and grew poorly at ambient CO2 partial pressure. Reduction in CA activity also increased the CO2 partial pressure required to saturate CO2 assimilation rates. The present data show that CA activity is essential for the functioning of the C4 photosynthetic pathway.
    Type of Medium: Electronic Resource
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  • 3
    Publication Date: 2008-12-01
    Print ISSN: 0008-4476
    Electronic ISSN: 1499-1276
    Topics: Geosciences
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