Copyright © Physiologia Plantarum 1999 PHYSIOLOGIA PLANTARUM 105: 670 – 678. 1999
Printed in Ireland —all rights resered ISSN 0031-9317
Flavodoxin accumulation contributes to enhanced cyclic electron flow
around photosystem I in salt-stressed cells of Synechocystis sp. strain
PCC 6803
Martin Hagemann
a,
*, Robert Jeanjean
b
, Sabine Fulda
a
, Michel Havaux
c
, Francoise Joset
b
and Norbert Erdmann
a
a
Uniersita ¨t Rostock, FB Biologie, Doberaner Str. 143, D-18051 Rostock, Germany
b
LCB-CNRS, 31 Chemin J. Aiguier, 13402 Marseille Cedex 20, France
c
CEA/Cadarache, DSV, DEVM, Laboratoire d’Ecophysiologie de la Photosynthe `se, 13108 Saint -Paul -lez -Durance, France
*Corresponding author, e -mail: mh@boser.bio4.uni -rostock.de
Received 28 August 1998; revised 30 November 1998
raised salt concentrations and, as expected, to low iron contents. The salt-regulated accumulation of flavodoxin encoded by the
Salt-acclimated cells of wild type (WT) Synechocystis display isiB gene and its possible function were investigated in the
increased activity of photosystem I (PSI), primarily used for cyanobacterium Synechocystis sp. strain PCC 6803. In North-
increased cyclic electron transport capacity (Jeanjean et al. ern blot experiments, a slight increase of the isiB -specific mRNA
1993, Plant Cell Physiol 34: 1073 – 1079). In salt-acclimated was observed in salt-shocked and salt-acclimated cells. High
levels of flavodoxin protein were detected in cells acclimated to cells of the flavodoxin null mutant, the level of cyclic electron
342 mM NaCl. In order to analyze the function of flavodoxin flow was lower than in wild type cells. It was concluded that
flavodoxin plays a role as an alternative electron carrier, used in cyanobacterial salt acclimation, an insertion null mutant of
isiB was constructed. It was possible to adapt this mutant to for cyclic electron flow in salt-treated Synechocystis cells.
Introduction
Cyanobacteria are photoautotrophic organisms performing
oxygen-evolving photosynthesis like higher plants. As a result
of their 3 billion years of evolution, cyanobacteria are
presently found in almost all ecosystems, demonstrating their
remarkable capability for environmental acclimation. Accli-
mation to high or changing salinities includes two main
physiological processes in cyanobacteria: (1) active ion ex-
port; (2) accumulation of osmoprotective compounds. Syn-
thesis of salt stress-specific proteins allow these processes to
be performed (Joset et al. 1996). The first process, in partic-
ular, expresses an enhanced demand of energy. Therefore, it
is not surprising that salt-induced changes in the cyanobacte-
rial photosynthetic activity and respiration have been studied.
A slightly enhanced content and a doubling of activity of
photosystem I (PSI) have been reported to be characteristic
for salt-loaded cells of Synechocystis sp. PCC 6803 and other
strains (Jeanjean et al. 1993, Schubert et al. 1993, Hibino et
al. 1996, Murakami et al. 1997). These changes lead to an
enhanced cyclic electron flow around PSI (Hibino et al. 1996,
Jeanjean et al. 1998), which facilitates higher ATP produc-
tion, necessary for primary and secondary active ion export
mechanisms. Furthermore, an increase in respiratory oxygen
consumption, which is accompanied by enhanced activity and
content of cytochrome oxidase, was also often found in
salt-stressed cyanobacterial cells (Gabbay-Azaria et al. 1992,
Peschek et al. 1994).
A protein which accumulated in salt-acclimated cells of
Synechocystis, could be identified as a flavodoxin (Fulda and
Hagemann 1995). Flavodoxin is a small soluble electron
carrier, which can functionally replace ferredoxin for almost
all of its functions (e.g. photosynthetic electron transport,
nitrate reduction, fatty acid desaturation) (Straus 1994). Only
glutamate synthase (GltS) seems to be solely dependent on
ferredoxin in Synechocystis (Schmitz et al. 1996). In cells of
Synechococcus sp. strain PCC 7002, a close binding of
flavodoxin to PSI has been demonstrated by chemical
Abbreiations – Chl a : chlorophyll a ; DCMU: 3-(3,4-dichlorophenyl)-1,1-dimethylurea; FNR: ferriedoxin/NADP
+
-oxidoreductase; Km:
kanamycin; NDH: NAD(P)H-dehydrogenase; PSI: photosystem I; PSII: photosystem II; WT: wild type.
Physiol. Plant. 105, 1999 670