Inactivation of photosynthetic cyclic electron transports upregulates photorespiration for compensation of efficient photosynthesis in Arabidopsis

Plants have multiple mechanisms to maintain efficient photosynthesis. Photosynthetic cyclic electron transports around photosystem I (CET), which includes the PGR5/PGRL1 and NDH pathways, and photorespiration play a crucial role in photosynthetic efficiency. However, how these two mechanisms are functionally linked is not clear. In this study, we revealed that photorespiration could compensate for the function of CET in efficient photosynthesis by comparison of the growth phenotypes, photosynthetic properties monitored with chlorophyll fluorescence parameters and photosynthetic oxygen evolution in leaves and photorespiratory activity monitored with the difference of photosynthetic oxygen evolution rate under high and low concentration of oxygen conditions between the deleted mutant PGR5 or PGRL1 under NDH defective background (pgr5 crr2 or pgrl1a1b crr2). Both CET mutants pgr5 crr2 and pgrl1a1b crr2 displayed similar suppression effects on photosynthetic capacities of light reaction and growth phenotypes under low light conditions. However, the total CET activity and photosynthetic oxygen evolution of pgr5 crr2 were evidently lower than those of pgrl1a1b crr2, accompanied by the upregulation of photorespiratory activity under low light conditions, resulting in severe suppression of photosynthetic capacities of light reaction and finally photodamaged phenotype under high light or fluctuating light conditions. Based on these findings, we suggest that photorespiration compensates for the loss of CET functions in the regulation of photosynthesis and that coordination of both mechanisms is essential for maintaining the efficient operation of photosynthesis, especially under stressed conditions

Valley polarization in MoS2 monolayers by optical pumping

We report experimental evidences on selective occupation of the degenerate valleys in MoS2 monolayers by circularly polarized optical pumping. Over 30% valley polarization has been observed at K and K' valley via the polarization resolved luminescence spectra on pristine MoS2 monolayers. It demonstrates one viable way to generate and detect valley polarization towards the conceptual valleytronics applications with information carried by the valley index

Short Communication Response of NAD(P)H dehydrogenase complex to the alteration of CO 2 concentration in the cyanobacterium Synechocystis PCC6803

Summary An NADPH-specific NDH-1 sub-complex was separated by native-polyacrylamide gel electrophoresis and detected by activity staining from the whole cell extracts of Synechocystis PCC6803. Low CO 2 caused an increase in the activity of this sub-complex quickly, accompanied by an evident increase in the expression of NdhK and PSI-driven NADPH oxidation activity that can reflect the activity of NDH-1-mediated cyclic electron transport. During incubation with high CO 2 , the activities of NDH-1 sub-complex and PSI-driven NADPH oxidation as well as the protein level of NdhK slightly increased at the beginning, but decreased evidently in various degrees along with incubation time. These results suggest that CO 2 concentration in vitro as a signal can control the activity of NDH-1 complex, and NDH-1 complex may in turn function in the regulation of CO 2 uptake. Key words: CO 2 concentration -CO 2 uptake -NAD(P)H dehydrogenase -Synechocystis PCC6803 Abbreviations: CCM = CO 2 concentrating mechanism. -DCMU = 3-(3,4-dichlorophenyl)-1,1-dimethylurea. -H-cells = cells grown in high CO 2 . -L-cells = cells grown in low CO 2 . -NBT = nitroblue tetrazolium. -NDH-1 = type 1 NAD(P)H dehydrogenase. -PAGE = polyacrylamide gel electrophoresi

The role of carotenoid isomerase in maintenance of photosynthetic oxygen evolution in rice plant

Carotenoid isomerase (CRTISO) has been suggested to protect photosystem II (PS II) from photodamage, probably through its product lutein. However, the mechanism of the photoprotection still remains to be further elucidated. In this work, we cloned a point mutated gene reported to encode a CRTISO which is responsible for the accumulation of lutein in rice mutant zel1 by a mapbased cloning approach. The mutant phenotype was rescued by transformation with the corresponding gene of the wild type (WT). The activity of photosynthetic oxygen evolution was evidently suppressed in zel1. The amount of the core protein of PS II CP47 was much lower in all the PS II complexes especially in the LHCII-PS II supercomplexes and CP43-free PS II of zel1 than that of WT. On the other hand, the amount of another core protein of PS II CP43 of zel1 was decreased in the higher supercomplexes, whereas it was increased in the lower ones and PS II monomer. The immunodetection displayed that CP43, CP47, and the oxygen-evolving extrinsic proteins PsbO and PsbP were reduced, but the amount of reaction center protein D1 did not show significant change in zel1. Northern blot analysis showed that the transcriptional level of CP43 was down-regulated but not that of CP47 or D1 in zel1. In addition, the plastoquinone (PQ) Q A was in a reduced state in zel1. On the basis of the results, we suggest that CRTISO might function in regulating the transcription of CP43 and the translation of CP47 by affecting the redox state of the PQ to stabilize the extrinsic proteins of oxygen evolution complexes in the rice plant

Redox regulation of Tobacco Rubisco activase mediated by thioredoxin-<i>f</i>

We measured the activation activities of RCA from spinach,arabidopsis,tobacco and tomato under different redox states in the presence of Trx-f from spinach and tobacco,respectively.The results showed that the activity of RCA from spinach and Arabidopsis was regulated by different redox states in the presence of Trx-f from spinach,and the activity of RCA from tobacco and tomato was regulated by different redox states in the presence of Trx-f from tobacco.It demonstrated that that both the activity of RCA consisted of two isoforms and only one isoform (like tobacco) can be regulated by changes in the redox states,which mediated by the Trx-f.Furthermore,we also suggested changes in the redox state of RCA mediated by Trx-f are species dependent

NdhV subunit regulates the activity of type-1 NAD(P)H dehydrogenase under high light conditions in cyanobacterium Synechocystis sp PCC 6803

The cyanobacterial NAD(P)H dehydrogenase (NDH-1) complexes play crucial roles in variety of bioenergetic reactions. However, the regulative mechanism of NDH-1 under stressed conditions is still unclear. In this study, we detected that the NDH-1 activity is partially impaired, but the accumulation of NDH-1 complexes was little affected in the NdhV deleted mutant (Delta ndhV) at low light in cyanobacterium Synechocystis sp. PCC 6803. Delta ndhV grew normally at low light but slowly at high light under inorganic carbon limitation conditions (low pH or low CO2), meanwhile the activity of CO2 uptake was evidently lowered than wild type even at pH 8.0. The accumulation of NdhV in thylakoids strictly relies on the presence of the hydrophilic subcomplex of NDH-1. Furthermore, NdhV was co-located with hydrophilic subunits of NDH-1 loosely associated with the NDH-1L, NDH-1MS' and NDH-1M complexes. The level of the NdhV was significantly increased at high light and deletion of NdhV suppressed the up-regulation of NDH-1 activity, causing the lowered the photosynthetic oxygen evolution at pH 6.5 and high light. These data indicate that NdhV is an intrinsic subunit of hydrophilic subcomplex of NDH-1, required for efficient operation of cyclic electron transport around photosystem I and CO2 uptake at high lights