TY - JOUR
T1 - Complete tracking of proton flow in thylakoids-the unit conductance of CF0 is greater than 10 fS
AU - Schoenknecht, Gerald
AU - Junge, Wolfgang
AU - Lill, H.
AU - Engelbrecht, Siegfried
PY - 1986/7/28
Y1 - 1986/7/28
N2 - We investigated the proton conductance of the channel portion of chloroplast ATP synthase (CF0). Thylakoids were CF1-depleted by EDTA treatment. Proton pumps were stimulated by short flashes of light. Proton flux through CF0 was measured spectrophotometrically in three different ways: as proton efflux from the lumen (via neutral red), charge flow across the membrane (via electrochromism) and proton influx into the medium (via phenol red). Hence we completely tracked the protons on their way from the lumen through CF0 into the medium. A first treatment with EDTA removed up to 12% of total CF1 without increasing the proton permeability of the membranes. A second treatment removed a further 20% of CF1 and increased the proton permeability of membranes by 3 orders of magnitude. The electric potential difference and the pH transients, in both the lumen and medium, decayed with a relaxation time of 7 ms indicating electrically driven proton flow through CF0. If the electric driving force was shunted (e.g. by added gramicidin) both pH transients decayed at 85 ms compared with 20-60 s in control thylakoids. The longer relaxation time under chemical driving force was attributable to larger chemical than electrical capacitance of thylakoids. We calculated a lower limit of the unit conductance of CF0 under the assumption that all exposed CF0 were proton conducting. The value was 10 fS, corresponding to the passage of 6200 protons/s per CF0 (at 100 mV electric driving force) and by orders of magnitude higher than so far reported for any F0 channel.
AB - We investigated the proton conductance of the channel portion of chloroplast ATP synthase (CF0). Thylakoids were CF1-depleted by EDTA treatment. Proton pumps were stimulated by short flashes of light. Proton flux through CF0 was measured spectrophotometrically in three different ways: as proton efflux from the lumen (via neutral red), charge flow across the membrane (via electrochromism) and proton influx into the medium (via phenol red). Hence we completely tracked the protons on their way from the lumen through CF0 into the medium. A first treatment with EDTA removed up to 12% of total CF1 without increasing the proton permeability of the membranes. A second treatment removed a further 20% of CF1 and increased the proton permeability of membranes by 3 orders of magnitude. The electric potential difference and the pH transients, in both the lumen and medium, decayed with a relaxation time of 7 ms indicating electrically driven proton flow through CF0. If the electric driving force was shunted (e.g. by added gramicidin) both pH transients decayed at 85 ms compared with 20-60 s in control thylakoids. The longer relaxation time under chemical driving force was attributable to larger chemical than electrical capacitance of thylakoids. We calculated a lower limit of the unit conductance of CF0 under the assumption that all exposed CF0 were proton conducting. The value was 10 fS, corresponding to the passage of 6200 protons/s per CF0 (at 100 mV electric driving force) and by orders of magnitude higher than so far reported for any F0 channel.
KW - CF
KW - H-ATPase
KW - Photosynthesis
KW - Unit conductance
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U2 - 10.1016/0014-5793(86)80760-8
DO - 10.1016/0014-5793(86)80760-8
M3 - Article
AN - SCOPUS:0012633142
SN - 0014-5793
VL - 203
SP - 289
EP - 294
JO - FEBS Letters
JF - FEBS Letters
IS - 2
ER -