Regulation of pepc gene expression in Anabaena sp. PCC 7120 and its effects on cyclic electron flow around photosystem I and tolerances to environmental stresses.

Since pepc gene encoding phosphoenolpyruvate carboxylase (PEPCase) has been cloned from Anabaena sp. PCC 7120 and other cyanobacteria, the effects of pepc gene expression on photosynthesis have not been reported yet. In this study, we constructed mutants containing either upregulated (forward) or downregulated (reverse) pepc gene in Anabaena sp.

Recombinant expression and functional analysis of a Chlamydomonas reinhardtii bacterial-type phosphoenolpyruvate carboxylase gene fragment.

To investigate the function of a bacterial-type phosphoenolpyruvate carboxylase (PEPC2) derived from photosynthetically-grown Chlamydomonas reinhardtii, a fragment of the pepc2 gene was cloned and expressed in Escherichia coli. After optimal induction for 6 h, PEPC activity in the reverse mutant was lower than wild type (0.9 vs.

A mutation of OSOTP 51 leads to impairment of photosystem I complex assembly and serious photo-damage in rice.

Gene expression in chloroplasts is regulated by many nuclear-encoded proteins. In this study, we isolated a rice (Oryza sativa subsp. japonica) mutant osotp51 with significant reduction in photosystem I (PSI).

Reversible association of ribulose-1, 5-bisphosphate carboxylase/oxygenase activase with the thylakoid membrane depends upon the ATP level and pH in rice without heat stress.

Ribulose-1, 5-bisphosphate carboxylase/oxygenase (Rubisco) activase (RCA) in the thylakoid membrane (TM) has been shown to play a role in protection and regulation of photosynthesis under moderate heat stress. However, the physiological significance of RCA bound to the TM (TM-RCA) without heat stress remains unknown. In this study, it is first shown, using experiments in vivo, that the TM-RCA varies in rice leaves at different development stages, under different environmental conditions, and in a rice mutant.

Construction of a chloroplast protein interaction network and functional mining of photosynthetic proteins in Arabidopsis thaliana.

Chloroplast is a typical plant cell organelle where photosynthesis takes place. In this study, a total of 1,808 chloroplast core proteins in Arabidopsis thaliana were reliably identified by combining the results of previously published studies and our own predictions. We then constructed a chloroplast protein interaction network primarily based on these core protein interactions.

[The progress in research on the reduced nicotinamide adenine di(tri)-nucleotide phosophate [NAD(P)H] dehydrogenase complex and chlororespiration].

Besides the non-cyclic electron transport driven by the two photosystems (PSII and PSI), the cyclic electron transport pathways around PSI are also essential for efficient photosynthesis. As one of these pathways, the NAD(P)H dehydrogenase complex (NDH complex) mediated cyclic electron transport has been well studied. Along with the identification of the plastid terminal oxydase (PTOX), the functions of NDH-mediated cyclic and chlororepiratory electron transport in energy supply for photosynthesis as well as in the resistance to photooxidative stress have increasingly been brought to the researchers' attention.

[Differences in plant hormone level of cucumber seedlings grown under sulfur or xenon lamp].

The primary mechanism of growth difference of cucumber (Cucumis sativus L.) seedlings cultured under sulfur lamp and xenon lamp in a phytotron was investigated. Compared with cucumber seedlings grown under xenon lamp, those under sulfur lamp were shorter, and the cell number in the middle hypocotyls epidermis and cortex of them were more (Fig.

[Separation of hydrophobic NAD(P)H dehydrogenase subcomplexes from cyanobacterium Synechocystis PCC6803].

Many efforts have been paid to the separation of an integrated NA(D)PH dehydrogenase (NDH) complex. Several hydrophilic subcomplexes of NDH have been purified from the cyanobacterium Synechocystis PCC6803. However, no hydrophobic NDH subcomplex has ever been separated from cyanobacteria yet.

The Involvement of Plastoquinone in the Pyocyanine-mediated Cyclic Electron Transport around Photosystem I.

2,5 dibromo-3-methyl-5-isopropyl-p-benzoquinone (DBMIB), an inhibitor of plastoquinone, inhibited photosystem I cyclic electron transport mediated by pyocyanine of low concentration, but had no effect on that mediated by phenazine methosulphate (PMS). In the presence of pyocyanine, the thylakoids displayed a transient post-illumination increase in chlorophyll fluorescence which resembled that displayed in leaves. The above results indicate the involvement of plastoquinone in the pyocyanine-mediated cyclic electron transport around photosystem I.