Evidence for slow turnover in a fraction of Photosystem II complexes in thylakoid membranes

R. A. Chylla, G. Garab, J. Whitmarsh

Research output: Contribution to journalArticle

77 Citations (Scopus)

Abstract

We used two different techniques to measure the recovery time of Photosystem II following the transfer of a single electron from P-680 to QA in thylakoid membranes isolated from spinach. Electron transfer in Photosystem II reaction centers was probed first by spectroscopic measurements of the electrochromic shift at 518 nm due to charge separation within the reaction centers. Using two short actinic flashes separated by a variable time interval we determined the time required after the first flash for the electrochromic shift at 518 nm to recover to the full extent on the second flash. In the second technique the redox state of QA at variable times after a saturating flash was monitored by measurement of the fluorescence induction in the absence of an inhibitor and in the presence of ferricyanide. The objective was to determine the time required after the actinic flash for the fluorescence induction to recover to the value observed after a 60 s dark period. Measurements were done under conditions in which (1) the electron donor for Photosystem II was water and the acceptor was the endogenous plastoquinone pool, and (2) Q400, the Fe2+ near QA, remained reduced and therefore was not a participant in the flash-induced electron-transfer reactions. The electrochromic shift at 518 nm and the fluorescence induction revealed a prominent biphasic recovery time for Photosystem II reaction centers. The majority of the Photosystem II reaction centers recovered in less than 50 ms. However, approx. one-third of the Photosystem II reaction centers required a half-time of 2-3 s to recover. Our interpretation of these data is that Photosystem II reaction centers consist of at least two distinct populations. One population, typically 68% of the total amount of Photosystem II as determined by the electrochromic shift, has a steady-state turnover rate for the electron-transfer reaction from water to the plastoquinone pool of approx. 250 e- / s, sufficiently rapid to account for measured rates of steady-state electron transport. The other population, typically 32%, has a turnover rate of approx. 0.2 e- / s. Since this turnover rate is over 1000-times slower than normally active Photosystem II complexes, we conclude that the slowly turning over Photosystem II complexes are inconsequential in contributing to energy transduction. The slowly turning over Photosystem II complexes are able to transfer an electron from P-680 to QA rapidly, but the reoxidation of Q-A is slow (t 1 2 = 2 s). The fluorescence induction measurements lead us to conclude that there is significant overlap between the slowly turning over fraction of Photosystem II complexes and PS IIβ reaction centers. One corollary of this conclusion is that electron transfer from P-680 to QA in PS IIβ reaction centers results in charge separation across the membrane and gives rise to an electrochromic shift.

Original languageEnglish
Pages (from-to)562-571
Number of pages10
JournalBBA - Bioenergetics
Volume894
Issue number3
DOIs
Publication statusPublished - Dec 17 1987

Fingerprint

Thylakoids
Photosystem II Protein Complex
Membranes
Electrons
Fluorescence
Plastoquinone
Population
Recovery
Spinacia oleracea
Water
Electron Transport
Oxidation-Reduction

Keywords

  • Electron transfer
  • Photosystem II
  • Reaction center turnover
  • Recovery time

ASJC Scopus subject areas

  • Biophysics

Cite this

Evidence for slow turnover in a fraction of Photosystem II complexes in thylakoid membranes. / Chylla, R. A.; Garab, G.; Whitmarsh, J.

In: BBA - Bioenergetics, Vol. 894, No. 3, 17.12.1987, p. 562-571.

Research output: Contribution to journalArticle

@article{261f7c9fa8114637a002b77fb0cf2e41,
title = "Evidence for slow turnover in a fraction of Photosystem II complexes in thylakoid membranes",
abstract = "We used two different techniques to measure the recovery time of Photosystem II following the transfer of a single electron from P-680 to QA in thylakoid membranes isolated from spinach. Electron transfer in Photosystem II reaction centers was probed first by spectroscopic measurements of the electrochromic shift at 518 nm due to charge separation within the reaction centers. Using two short actinic flashes separated by a variable time interval we determined the time required after the first flash for the electrochromic shift at 518 nm to recover to the full extent on the second flash. In the second technique the redox state of QA at variable times after a saturating flash was monitored by measurement of the fluorescence induction in the absence of an inhibitor and in the presence of ferricyanide. The objective was to determine the time required after the actinic flash for the fluorescence induction to recover to the value observed after a 60 s dark period. Measurements were done under conditions in which (1) the electron donor for Photosystem II was water and the acceptor was the endogenous plastoquinone pool, and (2) Q400, the Fe2+ near QA, remained reduced and therefore was not a participant in the flash-induced electron-transfer reactions. The electrochromic shift at 518 nm and the fluorescence induction revealed a prominent biphasic recovery time for Photosystem II reaction centers. The majority of the Photosystem II reaction centers recovered in less than 50 ms. However, approx. one-third of the Photosystem II reaction centers required a half-time of 2-3 s to recover. Our interpretation of these data is that Photosystem II reaction centers consist of at least two distinct populations. One population, typically 68{\%} of the total amount of Photosystem II as determined by the electrochromic shift, has a steady-state turnover rate for the electron-transfer reaction from water to the plastoquinone pool of approx. 250 e- / s, sufficiently rapid to account for measured rates of steady-state electron transport. The other population, typically 32{\%}, has a turnover rate of approx. 0.2 e- / s. Since this turnover rate is over 1000-times slower than normally active Photosystem II complexes, we conclude that the slowly turning over Photosystem II complexes are inconsequential in contributing to energy transduction. The slowly turning over Photosystem II complexes are able to transfer an electron from P-680 to QA rapidly, but the reoxidation of Q-A is slow (t 1 2 = 2 s). The fluorescence induction measurements lead us to conclude that there is significant overlap between the slowly turning over fraction of Photosystem II complexes and PS IIβ reaction centers. One corollary of this conclusion is that electron transfer from P-680 to QA in PS IIβ reaction centers results in charge separation across the membrane and gives rise to an electrochromic shift.",
keywords = "Electron transfer, Photosystem II, Reaction center turnover, Recovery time",
author = "Chylla, {R. A.} and G. Garab and J. Whitmarsh",
year = "1987",
month = "12",
day = "17",
doi = "10.1016/0005-2728(87)90136-8",
language = "English",
volume = "894",
pages = "562--571",
journal = "Biochimica et Biophysica Acta - Bioenergetics",
issn = "0005-2728",
publisher = "Elsevier",
number = "3",

}

TY - JOUR

T1 - Evidence for slow turnover in a fraction of Photosystem II complexes in thylakoid membranes

AU - Chylla, R. A.

AU - Garab, G.

AU - Whitmarsh, J.

PY - 1987/12/17

Y1 - 1987/12/17

N2 - We used two different techniques to measure the recovery time of Photosystem II following the transfer of a single electron from P-680 to QA in thylakoid membranes isolated from spinach. Electron transfer in Photosystem II reaction centers was probed first by spectroscopic measurements of the electrochromic shift at 518 nm due to charge separation within the reaction centers. Using two short actinic flashes separated by a variable time interval we determined the time required after the first flash for the electrochromic shift at 518 nm to recover to the full extent on the second flash. In the second technique the redox state of QA at variable times after a saturating flash was monitored by measurement of the fluorescence induction in the absence of an inhibitor and in the presence of ferricyanide. The objective was to determine the time required after the actinic flash for the fluorescence induction to recover to the value observed after a 60 s dark period. Measurements were done under conditions in which (1) the electron donor for Photosystem II was water and the acceptor was the endogenous plastoquinone pool, and (2) Q400, the Fe2+ near QA, remained reduced and therefore was not a participant in the flash-induced electron-transfer reactions. The electrochromic shift at 518 nm and the fluorescence induction revealed a prominent biphasic recovery time for Photosystem II reaction centers. The majority of the Photosystem II reaction centers recovered in less than 50 ms. However, approx. one-third of the Photosystem II reaction centers required a half-time of 2-3 s to recover. Our interpretation of these data is that Photosystem II reaction centers consist of at least two distinct populations. One population, typically 68% of the total amount of Photosystem II as determined by the electrochromic shift, has a steady-state turnover rate for the electron-transfer reaction from water to the plastoquinone pool of approx. 250 e- / s, sufficiently rapid to account for measured rates of steady-state electron transport. The other population, typically 32%, has a turnover rate of approx. 0.2 e- / s. Since this turnover rate is over 1000-times slower than normally active Photosystem II complexes, we conclude that the slowly turning over Photosystem II complexes are inconsequential in contributing to energy transduction. The slowly turning over Photosystem II complexes are able to transfer an electron from P-680 to QA rapidly, but the reoxidation of Q-A is slow (t 1 2 = 2 s). The fluorescence induction measurements lead us to conclude that there is significant overlap between the slowly turning over fraction of Photosystem II complexes and PS IIβ reaction centers. One corollary of this conclusion is that electron transfer from P-680 to QA in PS IIβ reaction centers results in charge separation across the membrane and gives rise to an electrochromic shift.

AB - We used two different techniques to measure the recovery time of Photosystem II following the transfer of a single electron from P-680 to QA in thylakoid membranes isolated from spinach. Electron transfer in Photosystem II reaction centers was probed first by spectroscopic measurements of the electrochromic shift at 518 nm due to charge separation within the reaction centers. Using two short actinic flashes separated by a variable time interval we determined the time required after the first flash for the electrochromic shift at 518 nm to recover to the full extent on the second flash. In the second technique the redox state of QA at variable times after a saturating flash was monitored by measurement of the fluorescence induction in the absence of an inhibitor and in the presence of ferricyanide. The objective was to determine the time required after the actinic flash for the fluorescence induction to recover to the value observed after a 60 s dark period. Measurements were done under conditions in which (1) the electron donor for Photosystem II was water and the acceptor was the endogenous plastoquinone pool, and (2) Q400, the Fe2+ near QA, remained reduced and therefore was not a participant in the flash-induced electron-transfer reactions. The electrochromic shift at 518 nm and the fluorescence induction revealed a prominent biphasic recovery time for Photosystem II reaction centers. The majority of the Photosystem II reaction centers recovered in less than 50 ms. However, approx. one-third of the Photosystem II reaction centers required a half-time of 2-3 s to recover. Our interpretation of these data is that Photosystem II reaction centers consist of at least two distinct populations. One population, typically 68% of the total amount of Photosystem II as determined by the electrochromic shift, has a steady-state turnover rate for the electron-transfer reaction from water to the plastoquinone pool of approx. 250 e- / s, sufficiently rapid to account for measured rates of steady-state electron transport. The other population, typically 32%, has a turnover rate of approx. 0.2 e- / s. Since this turnover rate is over 1000-times slower than normally active Photosystem II complexes, we conclude that the slowly turning over Photosystem II complexes are inconsequential in contributing to energy transduction. The slowly turning over Photosystem II complexes are able to transfer an electron from P-680 to QA rapidly, but the reoxidation of Q-A is slow (t 1 2 = 2 s). The fluorescence induction measurements lead us to conclude that there is significant overlap between the slowly turning over fraction of Photosystem II complexes and PS IIβ reaction centers. One corollary of this conclusion is that electron transfer from P-680 to QA in PS IIβ reaction centers results in charge separation across the membrane and gives rise to an electrochromic shift.

KW - Electron transfer

KW - Photosystem II

KW - Reaction center turnover

KW - Recovery time

UR - http://www.scopus.com/inward/record.url?scp=0000994654&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=0000994654&partnerID=8YFLogxK

U2 - 10.1016/0005-2728(87)90136-8

DO - 10.1016/0005-2728(87)90136-8

M3 - Article

VL - 894

SP - 562

EP - 571

JO - Biochimica et Biophysica Acta - Bioenergetics

JF - Biochimica et Biophysica Acta - Bioenergetics

SN - 0005-2728

IS - 3

ER -