Quantum Yields of Photosystem II Electron Transport and Carbon Dioxide Fixation in C4 Plants

1990 ◽  
Vol 17 (5) ◽  
pp. 579 ◽  
Author(s):  
JP Krall ◽  
GE Edwards

The quantum yields of non-cyclic electron transport from photosystem II (determined from chlorophyll a fluorescence) and carbon dioxide assimilation were measured in vivo in representative species of the three subgroups of C4 plants (NADP-malic enzyme, NAD-malic enzyme and PEP-carboxykinase) over a series of intercellular CO2 concentrations (CI) at both 21% and 2% O2. The CO2 assimilation rate was independent of O2 concentration over the entire range of Ci (up to 500 μbar) in all three C4 subgroups. The quantum yield of PS II electron transport was similar, or only slightly greater, in 21% v. 2% O2 at all Ci values. In contrast, in the C3 species wheat there was a large O2 dependent increase in PS II quantum yield at low CO2, which reflects a high level of photorespiration. In the C4 plants, the relationship of the quantum yield of PS II electron transport to the quantum yield of CO2 fixation is linear suggesting that photochemical use of energy absorbed by PS II is tightly linked to CO2 fixation in C4 plants. This relationship is nearly identical in all three subgroups and may allow estimates of photosynthetic rates of C4 plants based on measurements of PS II photochemical efficiency. The results suggest that in C4 plants both the photoreduction of O2 and photorespiration are low, even at very limiting CO2 concentrations.

1999 ◽  
Vol 26 (3) ◽  
pp. 283 ◽  
Author(s):  
Congming Lu ◽  
Giuseppe Torzillo ◽  
Avigad Vonshak

The kinetic response of photosystem II (PS II) photochemistry in Spirulina platensis(Norstedt M2 ) to high salinity (0.75 M NaCl) was found to consist of two phases. The first phase, which was independent of light, was characterized by a rapid decrease (15–50%) in the maximal efficiency of PS II photochemistry (Fv /Fm), the efficiency of excitation energy capture by open PS II reaction centres (Fv′/Fm′), photochemical quenching (qp) and the quantum yield of PS II electron transport (Φ PS II) in the first 15 min, followed by a recovery up to about 80–92% of their initial levels within the next 2 h. The second phase took place after 4 h, in which further decline in above parameters occurred. Such a decline occurred only when the cells were incubated in the light, reaching levels as low as 45–70% of their initial levels after 12 h. At the same time, non-photochemical quenching (qN) and Q B -non-reducing PS II reaction centres increased significantly in the first 15 min and then recovered to the initial level during the first phase but increased again in the light in the second phase. The changes in the probability of electron transfer beyond QA (ψo) and the yield of electron transport beyond QA (φ Eo), the absorption flux (ABS/RC) and the trapping flux (TRo /RC) per PS II reaction centre also displayed two different phases. The causes responsible for the decreased quantum yield of PS II electron transport during the two phases are discussed.


1991 ◽  
Vol 18 (4) ◽  
pp. 369 ◽  
Author(s):  
JP Krall ◽  
GE Edwards ◽  
MSB Ku

The quantum yields of electron transport from photosystem II (PSII) (Φe, determined from chlorophyll a fluorescence), and CO2 assimilation (ΦCO2, photosynthetic rate/light intensity) were measured simultaneously in vivo with representative species of Flaveria which show a progression in development between C3 and C4 photosynthesis and in reduction of photorespiration. These were F. pringlei (C3), F. sonorensis (C3-C4, but lacking a C4 cycle), F. floridana (C3-C4, with partially functional C4 cycle), F. brownii (C4-like) and F. bidentis (C4). The level of PSII activity with varying CI under 210 mbar O2 was very similar in all species. However, the progressive development of C4 characteristics among the species produced an increased efficiency in utilisation of PSII derived energy for CO2 assimilation under 210 mbar O2, due to reduced photorespiratory losses at low CO2 levels. In all species, when photorespiration was limited by low O2 (20 mbar), there was a linear or near linear relationship between the quantum yield of PSII v. the quantum yield of CO2 fixation with varying intercellular levels of CO2 (Ci) indicating that CO2 fixation in this case is linked to PSII activity. When switching from 20 to 210 mbar O2 at atmosphere levels of CO2, there was a similar decrease in the efficiency in utilising PSII activity for CO2 assimilation at different light intensities, but the degree of sensitivity to O2 progressively decreased among the species concomitant with the development of C4 photosynthesis. These results may help explain why there is an advantage to evolution of C4 photosynthesis in environments where Ci becomes limiting.


1993 ◽  
Vol 35 (3) ◽  
pp. 265-274 ◽  
Author(s):  
Walter Oberhuber ◽  
Zi-Yu Dai ◽  
Gerald E. Edwards

1991 ◽  
Vol 18 (3) ◽  
pp. 267 ◽  
Author(s):  
JP Krall ◽  
GE Edwards

The partitioning of light energy absorbed by photosystem (PS) II in the C4 species maize was investigated under various photosynthetic photon flux densities (PPFD), temperatures, and intercellular CO2 concentrations. The relationship between the quantum yield of PSII electron transport (�e) and the quantum yield of CO2 assimilation (ΦCO2) was generally found to be linear, with similar slopes. This indicates that PSII electron transport is tightly coupled to CO2 assimilation such that measurements of �e may be used to estimate photosynthetic rates in maize. Coefficients of quenching of PSII chlorophyll fluorescence indicated that, under excessive PPFD or when CO2 assimilation was decreased due to suboptimal or supraoptimal temperature or low Ci, the energy in excess of that needed to drive the reduced rate of PSII electron transport was dissipated via a mechanism known to be correlated to the trans-thylakoid proton gradient (high energy quenching, qE) and a mechanism believed to arise in the PSII antenna chlorophyll (qN(slow)). At suboptimal temperature the energy dissipation was principally at the antenna level and qE was low, while at supraoptimal temperature the reverse was true. The results are discussed relative to coupling of PSII activity to CO2 fixation and mechanisms of energy dissipation in this C4 species.


1990 ◽  
Vol 17 (1) ◽  
pp. 1 ◽  
Author(s):  
RT Furbank ◽  
CLD Jenkins ◽  
MD Hatch

The relationship between overcycling of the C4 acid cycle in C4 photosynthesis (due to CO2 leakage) and the quantum yield of photosynthesis is considered. From a comparison of theoretical and measured quantum yields we suggest that the high efficiency of light utilisation by most C4 plants can only be explained by the mandatory involvement of both the Q-cycle and cyclic or pseudocyclic electron transport in the proton partitioning process. The existence of the Q-cycle mechanism may have been a prerequisite for the evolution of the C4 pathway.


1993 ◽  
Vol 48 (3-4) ◽  
pp. 163-167
Author(s):  
Koichi Yoneyama ◽  
Yoshihiro Nakajima ◽  
Masaru Ogasawara ◽  
Hitoshi Kuramochi ◽  
Makoto Konnai ◽  
...  

Abstract Through the studies on structure-activity relationships of 5-acyl-3-(1-aminoalkylidene)-4-hydroxy-2 H-pyran-2,6(3 H)-dione derivatives in photosystem II (PS II) inhibition, overall lipophilicity of the molecule was found to be a major determinant for the activity. In the substituted N -benzyl derivatives, not only the lipophilicity but also the electronic and steric characters of the substituents greatly affected the activity. Their mode of PS II inhibition seemed to be similar to that of DCMU , whereas pyran-enamine derivatives needed to be highly lipophilic to block the electron transport in thylakoid membranes, which in turn diminished the permeability through biomembranes.


1991 ◽  
Vol 46 (1-2) ◽  
pp. 93-98 ◽  
Author(s):  
Helen G. McFadden ◽  
Donald C. Craig ◽  
John L. Huppatz ◽  
John N. Phillips

Abstract X-ray crystallographic data for the highly potent cyanoacrylate photosynthetic electron transport inhibitor, (Z)-ethoxyethyl 3-(4-chlorobenzylamino)-2-cyano-4-methylpent-2-enoate, are presented. This compound has a particularly high affinity for the photosystem II (PS II) herbicide receptor with a p I50 value of 9.5 (in the Hill reaction under uncoupled condi­tions with a chlorophyll concentration of 0.1 μg/ml). Data regarding the structure of small li­gands, such as this potent cyanoacrylate, which bind to the site with high affinity may be used to provide the basis for modelling studies of PS II/herbicide complexes. The X-ray data presented confirm the Z-stereochemistry of active cyanoacrylates and demonstrate the pres­ence of a planar core stabilized by an intramolecular hydrogen bond between the ester car­bonyl oxygen and a benzylamino hydrogen atom. In order to assess the importance of the benzylamino -NH -group in this type of cyanoacrylate, analogues containing a methylene group in its place were synthesized and found to be 100-and 1000-fold less active as Hill inhibitors.


1980 ◽  
Vol 35 (3-4) ◽  
pp. 293-297 ◽  
Author(s):  
P. V. Sane ◽  
Udo Johanningmeier

Abstract Low concentrations (10 µM) of tetranitromethane inhibit noncyclic electron transport in spinach chloroplasts. A study of different partial electron transport reactions shows that tetranitromethane primarily interferes with the electron flow from water to PS II. At higher concentrations the oxidation of plastohydroquinone is also inhibited. Because diphenyl carbazide but not Mn2+ ions can donate electrons efficiently to PS II in the presence of tetranitromethane it is suggested that it blocks the donor side of PS II prior to donation of electrons by diphenyl carbazide. The pH dependence of the inhibition by this protein modifying reagent may indicate that a functional-SH group is essential for a protein, which mediates electron transport between the water splitting complex and the reaction center of PS II.


1996 ◽  
Vol 51 (1-2) ◽  
pp. 47-52 ◽  
Author(s):  
W. I. Gruszecki ◽  
K. Strzałk ◽  
K.P. Bader ◽  
A. Radunz ◽  
G.H. Schmid

Abstract In our previous study (Gruszecki et al., 1995) we have postulated that the mechanism of cyclic electron transport around photosystem II, active under overexcitation of the photosynthetic apparatus by light is under control of the xanthophyll cycle. The combination of dif­ferent light quality and thylakoids having various levels of xanthophyll cycle pigments were applied to support this hypothesis. In the present work photosynthetic oxygen evolution from isolated tobacco chloroplasts was measured by means of mass spectrometry under conditions of high or low levels of violaxanthin, being transformed to zeaxanthin during dark incubation in an ascorbate containing buffer at pH 5.7. Analysis of oxygen evolution and of light-induced oxygen uptake indicate that the de-epoxidation of violaxanthin to zeaxanthin results in an increased cyclic electron transport around PS II, thus dimishing the vectorial electron flow from water. An effect similar to de-epoxidation was observed after incubation of thylakoid membranes with specific antibodies against violaxanthin.


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