| The Proton-Driven Rotor of ATP Synthase: Ohmic Conductance (10 fS), and Absence of Voltage Gating Biophysical Journal, Volume 86, Issue 6, 1 June 2004, Pages 4094-4109 Boris A. Feniouk, Maria A. Kozlova, Dmitry A. Knorre, Dmitry A. Cherepanov, Armen Y. Mulkidjanian and Wolfgang Junge Abstract The membrane portion of FF-ATP synthase, F, translocates protons by a rotary mechanism. Proton conduction by F was studied in chromatophores of the photosynthetic bacterium . The discharge of a light-induced voltage jump was monitored by electrochromic absorption transients to yield the unitary conductance of F. The current-voltage relationship of F was linear from 7 to 70mV. The current was extremely proton-specific (>10) and varied only slightly (≈threefold) from pH 6 to 10. The maximum conductance was ≈10 fS at pH 8, equivalent to 6240H s at 100-mV driving force, which is an order-of-magnitude greater than of coupled FF. There was no voltage-gating of F even at low voltage, and proton translocation could be driven by ΔpH alone, without voltage. The reported voltage gating in FF is thus attributable to the interaction of F with F but not to F proper. We simulated proton conduction by a minimal rotary model including the rotating -ring and two relay groups mediating proton exchange between the ring and the respective membrane surface. The data fit attributed pK values of ≈6 and ≈10 to these relays, and placed them close to the membrane/electrolyte interface. Abstract | Full Text | PDF (293 kb) |
| Expanding the club: engineering plants to talk to bacteria Trends in Plant Science, Volume 5, Issue 3, 1 March 2000, Pages 89-91 Leland S Pierson III Full Text | PDF (53 kb) |
| Nuclear magnetic resonance study of spin relaxation and magnetic field gradients in maple leaves Biophysical Journal, Volume 69, Issue 3, 1 September 1995, Pages 1111-1116 D.C. McCain Abstract 1H Nuclear magnetic resonance techniques were used to measure the distributions of spin-spin relaxation times, T2, and of magnetic field gradients in both the chloroplast and nonchloroplast water compartments of maple leaves (Acer platanoides). Results showed that encounters between water molecules and membranes inside chloroplasts provide an inefficient relaxation mechanism; i.e., chloroplast membranes interact weakly with water molecules. Gradient measurements indirectly measured the sizes of chloroplasts by showing that water in the chloroplasts is confined to small compartments a few microns in diameter. A comparison between measured gradients and gradients calculated for a model leaf indicated that chloroplasts are somewhat more likely to occupy positions along cell walls adjacent to air spaces, but also they may be found in the interiors of cells. Abstract | PDF (624 kb) |
Copyright © 1972 The Biophysical Society. All rights reserved.
Biophysical Journal, Volume 12, Issue 7, 839-850, 1 July 1972
doi:10.1016/S0006-3495(72)86127-7
Article
J.L. Rosenberg, S. Sahu and T.K. Bigat
Three independent methods have been used to determine the size of the quantum accumulation unit in green plant photosynthesis. This unit is defined as that group of pigment molecules within which quantal absorption acts must take place leading to the evolution of a single O2 molecule. All three methods take advantage of the nonlinearity of oxygen yield with light dose at very low dosages. The experimental values of this unit size, based on an assumed model for the charge cooperation in O2 evolution, ranging from 800 to 1600, suggest that there is either limited energy transfer between energy-trapping units or chemical cooperation among oxygen precursors formed in several neighboring energy-trapping units. Widely diffusible essential precursors to molecular oxygen are ruled out by these results. Inhibition studies show that O2 evolution is blocked when 3-(3,4-dichlorophenyl)-1,1-dimethylurea (DCMU) is added to chloroplasts after two preliminary flashes and before a third flash which would have yielded O2 in the absence of DCMU. This experiment is interpreted as evidence that the site of DCMU inhibition is on the oxidizing side of system II. Pretreatment of chloroplasts with large concentrations of Tris, previously believed to destroy O2 evolution by blocking an essential reaction in the electron chain between water and system II, may be alternately interpreted as promoting the dark reversal of the system II light-induced electron transfer.