A cDNA clone encoding a ferredoxin-NADP+ reductase from Chlamydomonas reinhardtii.

نویسندگان

  • M Kitayama
  • K Kitayama
  • R K Togasaki
چکیده

FNR (EC 1.18.1.2) is a flavoenzyme that plays an important role in the metabolism of photosynthetic organisms. FNR catalyzes the final step of the linear photosynthetic electron transfer chain by mediating the passage of electrons from reduced Fd to NADP+. FNR is situated at a branch point in electron flow, playing a key role in regulating the relative amounts of cyclic and noncyclic electron flow to meet the demands of the plant for ATP and reducing power. Besides these photosynthetic functions, recently FNR has been implicated in the defense response mechanisms against oxidative stress in Escherichia coli (Liochev et al., 1994). We report here the isolation of a cDNA clone encoding an FNR of the unicellular green alga Chlamydomonas reinhardtii (Table I). This clone was obtained as a false-positive signal from a cDNA library (Merchant and Bogorad, 1987) by antiphosphoglycerate kinase (EC 2.7.2.3) antibodies (Kitayama and Togasaki, 1992). The size of the cDNA insert of Chlamydomonas FNR is 1565 bp. The DNA sequence of Chlamydomonas FNR has 63, 57, and 58% homology with rice (Aoki and Ida, 1994), pea (Newman and Gray, 1988), and spinach FNR (Jansen et al., 1988), respectively. The deduced amino acid sequence of Chlamydomonas FNR has 59, 46, and 45% identity with rice, pea, and spinach FNR, respectively. Studies on the three-dimensional x-ray structure of FNR have focused on spinach FNR and the functions of amino acid residues have been assigned by Karplus et al. (1991). A11 of the amino acid residues that have been assigned specific functions, such as flavin adenine dinucleotide-binding residues and NADP-binding residues, have been well conserved in the FNR of Chlamydomonas. The homology within the putative N-terminal amino acid regions are very low when compared with N-terminal amino acid regions of a11 other species of FNRs. In addition, there is no significant identity of the putative transit peptide regions to the organellar FNR from spinach, pea, rice, and Cyanophora paradoxa (Jakowitsch et al., 1993).

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

Trypsin-sensitive photosynthetic activities in chloroplast membranes from Chlamydomonas reinhardi, y-1.

Location of electron transport chain components in chloroplast membranes of chlamydomonas reinhardi, y-1 was investigated by use of proteolytic digestion with soluble or insolubilized trypsin. Digestion of intact membrane vesicles with soluble trypsin inactivates the water-splitting system, the 3-(3,4-dichlorophenyl)-1,1-dimethylurea inhibition site of Photosystem II, the electron transport bet...

متن کامل

The chloroplast protein translocation complexes of Chlamydomonas reinhardtii: a bioinformatic comparison of Toc and Tic components in plants, green algae and red algae.

The recently completed genome of Chlamydomonas reinhardtii was surveyed for components of the chloroplast protein translocation complexes. Putative components were identified using reciprocal BlastP searches with the protein sequences of Arabidopsis thaliana as queries. As a comparison, we also surveyed the new genomes of the bryophyte Physcomitrella patens, two prasinophyte green algae (Ostreo...

متن کامل

In vitro reconstitution of electron transport from glucose-6-phosphate and NADPH to nitrite

An NADPH-dependent NO2--reducing system was reconstituted in vitro using ferredoxin (Fd) NADP+ oxidoreductase (FNR), Fd, and nitrite reductase (NiR) from the green alga Chlamydomonas reinhardtii. NO2- reduction was dependent on all protein components and was operated under either aerobic or anaerobic conditions. NO2- reduction by this in vitro pathway was inhibited up to 63% by 1 mm NADP+. NADP...

متن کامل

Localization of Nitrogen-Assimilating Enzymes in the Chloroplast of Chlamydomonas reinhardtii.

The specific activities of nitrate reductase, nitrite reductase, glutamine synthetase, glutamate synthase, and glutamate dehydrogenase were determined in intact protoplasts and intact chloroplasts from Chlamydomonas reinhardtii. After correction for contamination, the data were used to calculate the portion of each enzyme in the algal chloroplast. The chloroplast of C. reinhardtii contained all...

متن کامل

The dual effect of a ferredoxin-hydrogenase fusion protein in vivo: successful divergence of the photosynthetic electron flux towards hydrogen production and elevated oxygen tolerance

BACKGROUND Hydrogen photo-production in green algae, catalyzed by the enzyme [FeFe]-hydrogenase (HydA), is considered a promising source of renewable clean energy. Yet, a significant increase in hydrogen production efficiency is necessary for industrial scale-up. We have previously shown that a major challenge to be resolved is the inferior competitiveness of HydA with NADPH production, catalyz...

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

عنوان ژورنال:
  • Plant physiology

دوره 106 4  شماره 

صفحات  -

تاریخ انتشار 1994