Impact of iron limitation on the photosynthetic apparatus of the diatom Chaetoceros muelleri (Bacillariophyceae)

被引:51
作者
Davey, M [1 ]
Geider, RJ [1 ]
机构
[1] Marine Biol Assoc United Kingdom Lab, Plymouth PL1 2PB, Devon, England
关键词
Chaetoceros muelleri; flavodoxin; FRR; iron limitation; photosynthesis; photosystem II;
D O I
10.1046/j.1529-8817.2001.99169.x
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Iron starvation induced marked increases in flavodoxin abundance and decreases in light-saturated and light-limited photosynthesis rates in the diatom Chaetoceros muelleri. Consistent with the substitution of flavodoxin for ferredoxin as an early response to iron starvation, increases of flavodoxin abundance were observed before declines of cell division rate or chl a specific photosynthesis rates. Changes in the abundance of flavodoxin after the addition of iron to iron-starved cells indicated that flavodoxin was not actively degraded under iron-replete conditions. Greater declines in light-saturated oxygen evolution rates than dark oxygen consumption rates indicated that the mitochondrial electron transfer chain was not affected as greatly by iron starvation as the photosynthetic electron transfer chain. The carbon:nitrogen ratio was unaffected by iron starvation, suggesting that photosynthetic electron transfer was a primary target of iron starvation and that reductions in nitrate assimilation were due to energy limitation (die ON ratio would be expected to rise under nitrogen-limited but energy-replete conditions). Parallel changes were observed in the maximum light-saturated photosynthesis rate and the light-limited initial slope of the photosynthesis-light curve during iron starvation and recovery. The lowest photosynthesis rates were observed in iron-starved cells and the highest values in iron-replete cells. The light saturation parameter, I-k, was not affected by iron starvation, nor was the chl-to-C ratio markedly reduced. These observations were consistent with iron starvation having a similar or greater effect on photochemical charge separation in PSII than on downstream electron transfer steps. Declines of the ratio of variable to maximum fluorescence in iron-starved cells were consistent with PSII being a primary target of iron starvation. The functional cross-section of PSII was affected only marginally (< 20%) by iron starvation, with the largest values observed in iron-starved cells. The rate constant for electron transfer calculated from fast repetition rate fluorescence was found to covary with the light-saturated photosynthesis rate; it was lowest in the most severely starved cells.
引用
收藏
页码:987 / 1000
页数:14
相关论文
共 67 条
[1]   Compensatory changes in Photosystem II electron turnover rates protect photosynthesis from photoinhibition [J].
Behrenfeld, MJ ;
Prasil, O ;
Kolber, ZS ;
Babin, M ;
Falkowski, PG .
PHOTOSYNTHESIS RESEARCH, 1998, 58 (03) :259-268
[2]  
BEHRENFELD MJ, 1996, NATURE, V385, P505
[3]   Iron deficiency causes changes in chlorophyll fluorescence due to the reduction in the dark of the Photosystem II acceptor side [J].
Belkhodja, R ;
Morales, F ;
Quílez, R ;
López-Millán, AF ;
Abadía, A ;
Abadía, J .
PHOTOSYNTHESIS RESEARCH, 1998, 56 (03) :265-276
[4]   Acquisition and utilization of transition metal ions by marine organisms [J].
Butler, A .
SCIENCE, 1998, 281 (5374) :207-210
[5]   EFFECTS OF IRON AND OXYGEN ON CHLOROPHYLL BIOSYNTHESIS .2. OBSERVATIONS ON THE BIOSYNTHETIC-PATHWAY IN ISOLATED ETIOCHLOROPLASTS [J].
CHERESKIN, BM ;
CASTELFRANCO, PA .
PLANT PHYSIOLOGY, 1982, 69 (01) :112-116
[6]   A massive phytoplankton bloom induced by an ecosystem-scale iron fertilization experiment in the equatorial Pacific Ocean [J].
Coale, KH ;
Johnson, KS ;
Fitzwater, SE ;
Gordon, RM ;
Tanner, S ;
Chavez, FP ;
Ferioli, L ;
Sakamoto, C ;
Rogers, P ;
Millero, F ;
Steinberg, P ;
Nightingale, P ;
Cooper, D ;
Cochlan, WP ;
Landry, MR ;
Constantinou, J ;
Rollwagen, G ;
Trasvina, A ;
Kudela, R .
NATURE, 1996, 383 (6600) :495-501
[7]   Signal transduction and transcriptional and posttranscriptional control of iron-regulated genes in bacteria [J].
Crosa, JH .
MICROBIOLOGY AND MOLECULAR BIOLOGY REVIEWS, 1997, 61 (03) :319-+
[8]  
Davies BH, 1976, CHEMISTRY BIOCHEMIST, P38, DOI DOI 10.1590/S0101-20612001000200017
[9]   VONLIEBIG LAW OF THE MINIMUM AND PLANKTON ECOLOGY (1899-1991) [J].
DEBAAR, HJW .
PROGRESS IN OCEANOGRAPHY, 1994, 33 (04) :347-386
[10]   SOME EFFECTS OF IRON AND NITROGEN STRESS ON THE RED TIDE DINOFLAGELLATE GYMNODINIUM-SANGUINEUM [J].
DOUCETTE, GJ ;
HARRISON, PJ .
MARINE ECOLOGY PROGRESS SERIES, 1990, 62 (03) :293-306