Effects of External Mg2+ and Ph on the Photosynthetic Activities and Stromal pH of Intact Chloroplasts Isolated From C4 Plants

1989 ◽  
Vol 16 (5) ◽  
pp. 379
Author(s):  
S Boag ◽  
A Agostino ◽  
RT Furbank ◽  
MD Hatch

Exogenous Mg2+ inhibited PGA- and OAA-dependent photosynthetic O2 evolution by isolated mesophyll chloroplasts from Zea mays and also HCO3--dependent O2 evolution by chloroplasts from Panicum miliaceum bundle sheath cells. Inhibition of 50-75% was observed with 3-5 mM Mg2+; this varied to some extent with pH but was not reversed by K+ . Inhibition of HCO3-- and PGA-dependent O2 evolution by the divalent cation ionophore A23187 was reversed by adding Mg2+ . Notably, HCO3-- dependent O2 evolution by isolated bundle sheath cells from P. miliaceum was not inhibited by [Mg2+] up to 20 mM. Addition of Mg2+ in the light decreased the stromal pH of mesophyll chloroplasts by less than 0.2 units but reduced apparent stromal volume by as much as 25%. At least for bundle sheath chloroplasts, stromal pH varied with external pH over the range from 7 to 8 but remained about 0.3 units higher throughout this range. Oxygen evolution by isolated mesophyll chloroplasts, and bundle sheath cells and chloroplasts, was relatively insensitive to external pH in the range from 7 to 8. The results are considered in terms of likely mechanisms for the effects of exogenous Mg2+ and pH on photosynthesis by isolated chloroplasts and the physiological significance of Mg2+ effects.

1980 ◽  
Vol 7 (6) ◽  
pp. 655 ◽  
Author(s):  
H Usuda ◽  
GE Edwards

In isolated bundle sheath cells of P. capillare, glycerate is a major product of 14CO2 fixation at low bicarbonate concentrations. After 6 min of CO2 fixation at 0.34 mM NaHCO3, about 20% of the labelled products was in glycerate and about 45% in glycine plus serine. Inhibitors of the glycollate pathway prevented incorporation of label into glycerate. After 6 min of CO2 fixation at high bicarbonate concentration (20 mM NaH14CO3), a large percentage of the label was incorporated in phosphate esters, insolubles, and sucrose, and little label was observed in metabolites of the glycollate pathway. The results indicate glycerate is primarily formed through the glycollate pathway in bundle sheath cells rather than through 3-phosphoglycerate phosphatase. Glycerate-dependent oxygen evolution in the light and 14C incorporation into phosphate esters from [1-14C]glycerate was observed with mesophyll chloroplasts and mesophyll protoplasts, respectively, but not with bundle sheath cells. This is consistent with our previously published results that glycerate kinase is localized only in C4 mesophyll chloroplasts. Both isolated bundle sheath cells and mesophyll chloroplasts exhibited 3-phosphoglycerate dependent O2 evolution in the light indicating that the reductive phase of photosynthesis is functional in both cells. The results suggest that, during C4 photosynthesis, glycerate is synthesized by the glycollate pathway in bundle sheath cells and subsequently metabolized in mesophyll cells without direct linkage to the reductive pentose phosphate pathway.


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