The chloroplast tat pathway transports substrates in the dark

被引:11
作者
Braun, Nikolai A. [1 ]
Theg, Steven M. [1 ]
机构
[1] Univ Calif Davis, Dept Plant Biol, Davis, CA 95616 USA
关键词
D O I
10.1074/jbc.M708948200
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Photosynthetic electron transport pumps protons into the thylakoid lumen, creating an electrochemical potential called the protonmotive force (PMF). The energy of the thylakoid PMF is utilized by such machinery as the chloroplast F0F1-ATPase as well as the chloroplast Tat (cpTat) pathway ( a protein transporter) to do work. The bulk phase thylakoid PMF decays rapidly after the termination of actinic illumination, and it has been well established via potentiometric measurements that there is no detectable electrical or chemical potential in the thylakoid after a brief time in the dark. Yet, we report herein that cpTat transport can occur for long periods in the dark. We show that the thylakoid PMF is actually present long after actinic illumination of the thylakoids ceases and that this energy is present in physiologically useful quantities. Consistent with previous studies, the dark-persisting thylakoid potential is not detectable by established indicators. We propose that cpTat transport in the dark is dependent on a pool of protons in the thylakoid held out of equilibrium with those in the bulk aqueous phase.
引用
收藏
页码:8822 / 8828
页数:7
相关论文
共 51 条
[1]   Energetics of protein transport across biological membranes:: A study of the thylakoid ΔpH-dependent/cpTat pathway [J].
Alder, NN ;
Theg, SM .
CELL, 2003, 112 (02) :231-242
[2]  
ARANA JL, 1982, J BIOL CHEM, V257, P1125
[3]  
ARNON DI, 1949, PLANT PHYSIOL, V24, P15
[4]   NEUTRAL RED, A RAPID INDICATOR FOR PH-CHANGES IN INNER PHASE OF THYLAKOIDS [J].
AUSLANDER, W ;
JUNGE, W .
FEBS LETTERS, 1975, 59 (02) :310-315
[5]   Two electrical potential-dependent steps are required for transport by the Escherichia coli Tat machinery [J].
Bageshwar, Umesh K. ;
Musser, Siegfried M. .
JOURNAL OF CELL BIOLOGY, 2007, 179 (01) :87-99
[6]   Proton to electron stoichiometry in electron transport of spinach thylakoids [J].
Berry, S ;
Rumberg, B .
BIOCHIMICA ET BIOPHYSICA ACTA-BIOENERGETICS, 1999, 1410 (03) :248-261
[7]   TatB and TatC form a functional and structural unit of the twin-arginine translocase from Escherichia coli [J].
Bolhuis, A ;
Mathers, JE ;
Thomas, JD ;
Barrett, CML ;
Robinson, C .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (23) :20213-20219
[8]   The chloroplast tat pathway utilizes the transmembrane electric potential as an energy source [J].
Braun, Nikolai A. ;
Davis, Andrew W. ;
Theg, Steven M. .
BIOPHYSICAL JOURNAL, 2007, 93 (06) :1993-1998
[9]   Hypothesis-review -: An alternative model of the twin arginine translocation system [J].
Brüser, T ;
Sanders, C .
MICROBIOLOGICAL RESEARCH, 2003, 158 (01) :7-17
[10]  
CLINE K, 1992, J BIOL CHEM, V267, P2688