|1.||Long, Benedict M: 2 articles (09/2014 - 01/2012)|
|2.||Price, G Dean: 2 articles (09/2014 - 01/2012)|
|3.||Medrano, Hipólito: 2 articles (01/2011 - 01/2006)|
|4.||Galmés, Jeroni: 2 articles (01/2011 - 01/2006)|
|5.||Flexas, Jaume: 2 articles (01/2011 - 01/2006)|
|6.||Elsaied, Hosam Easa: 2 articles (01/2007 - 09/2006)|
|7.||Naganuma, Takeshi: 2 articles (01/2007 - 09/2006)|
|8.||Monakhova, O F: 2 articles (09/2003 - 11/2001)|
|9.||Cherniad'ev, I I: 2 articles (09/2003 - 11/2001)|
|10.||Nieuwland, Maaike: 1 article (11/2014)|
08/21/2008 - "The photochemical efficiency as the F(v)/F(m) ratio and the amount of RUBISCO were also determined under heat shock, water deficit, and under the combined action of both stress. "
11/01/2007 - "In these plants, the CO(2) assimilation rate was not affected by heat shock and there was a slight and non-significant reduction in maximum carboxylation velocity of Rubisco (V(cmax)) and maximum electron transport rate contributing to Rubisco regeneration (J(max)). "
11/01/2005 - "Finally, we report that almost all RuBisCO was retained in plastids prepared from cells subjected to a heat shock treatment, although cellular proteins were denatured by the treatment."
03/07/1995 - "Our results confirmed that activation of Rubisco by R-A is an ATP hydrolysis-dependent process and further demonstrated that (a) R-A binds preferably to non-native Rubisco protein, than to the native form, and dissociates from this complex after addition of ATP, (b) R-A increases during heat shock treatment in maize seedling leaves, and (c) a large recovery of Rubisco activity is achieved from heat-inactivated Rubisco by addition of R-A and an energy source. "
01/01/2013 - "Among the up-regulated proteins, we identified sucrose synthase (nodulin-100), β-tubulin, rubisco activase, glutathione-S-transferase, a putative heat-shock 70-kDa protein, pyridine nucleotide-disulphideoxidoreductase and a putative transposase. "
|2.||Dehydration (Water Stress)
01/01/2012 - "The shell of β-type carboxysomes is thought to be composed of two functional layers, with the inner layer involved in RuBisCO scaffolding and bicarbonate dehydration, and the outer layer in selective permeability to dissolved solutes. "
01/01/2011 - "The results confirmed species-specific patterns in the decrease in the initial activity and activation state of Rubisco as drought stress and leaf dehydration intensified. "
01/01/2011 - "Rubisco activity in Mediterranean species is regulated by the chloroplastic CO2 concentration under water stress."
05/01/2010 - "During leaf dehydration the quantity and maximum activity of Rubisco remained unchanged but the initial and total activities declined slightly, possibly due to increased inhibition. "
01/01/2006 - "It is suggested that the Rubisco specificity factor does not acclimate to water stress in the short term (weeks or months) in tobacco, and the validity of the so-called Laisk gas exchange method to estimate tau under drought is questioned."
01/01/2014 - "In conclusion, biochemical limitations likely related to the reduced activity of Rubisco, rather than diffusive limitations, were the main factor associated with decreases in A during the infection process of P. "
02/01/2005 - "This indicated that virus infection caused the decreases of Rubisco and RCA in host plant, which then affected plant photosynthesis."
02/01/2005 - "[Distribution of Rubisco and RCA in Brassica chinensis chloroplasts and effect of TuMV-infection on their cellular localization]."
01/01/2013 - "The infection reduced light saturation point, net photosynthesis at saturating irradiances, apparent quantum yield, CO2 saturated rate of photosynthesis, carboxylation efficiency, the maximum carboxylation rate of Rubisco, and maximum light-saturated rate of electron transport, and increased light compensation point in host leaves similarly across nitrate levels, corresponding to a similar magnitude of negative effects of the parasite on host leaf soluble protein and Rubisco concentrations, photosynthetic nitrogen use efficiency and stomatal conductance across nitrate concentrations. "
08/01/2011 - "Data obtained with saspases implicate them in the proteolytic degradation of ribulose-1,5-bisphosphate carboxylase/oxygenase (Rubisco) during biotic and abiotic PCD, whereas phytaspase overproducing and silenced transgenics provide evidence that phytaspase regulates PCD during both abiotic (oxidative and osmotic stresses) and biotic (virus infection) insults. "
04/01/1977 - "Comparisons of the isoelectric points of small and large subunits of ribulose biphosphate carboxylase extracted from a number of diploid, tetraploid, and hexaploid Avena species have been used to obtain information on the nuclear and cytoplasmic genome relationships within the genus. "
11/01/1993 - "Tetraploid potato clones, transgenic for the rolC gene of Agrobacterium rhizogenes under control of the light-inducible ribulose bisphosphate carboxylase small subunit promoter (rbcS-rolC), were compared, with respect to yield attributes and tuber carbohydrates, with transformed and untransformed controls and with 35S-rolC transgenic potato plants. "
04/15/1992 - "Sulfur starvation in Lemna leads to degradation of ribulose-bisphosphate carboxylase without plant death."
08/01/2003 - "Prominent effects observed during nitrogen starvation/limitation were: (i) reduction of major and accessory photosynthetic pigments, (ii) impairment of photosynthesis due to loss of one major Rubisco isoenzyme, (iii) reduced synthesis of lipids and fatty acids, (iv) modifications of protein synthesis leading to the repression of three polypeptides and synthesis of two new polypeptides, (v) enhanced glutamine synthetase and reduced nitrate reductase activities, (vi) enhanced production of hydrogen peroxide and (vii) induced appearance of four new peroxidase isoenzymes. "
|3.||ribulose-1,5 diphosphate (ribulose-1,5-bisphosphate)
|4.||Proteins (Proteins, Gene)
|5.||Tissue Plasminogen Activator (Alteplase)
|8.||Carbonic Anhydrases (Carbonic Anhydrase)
|9.||Photosystem II Protein Complex (Photosystem II)