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HORT640 - Metabolic Plant Physiology
References, sulfur assimilation or sulphur assimilation
Abdel-Ghany SE, Ye H, Garifullina GF, Zhang L, Pilon-Smits EA, Pilon M. Iron-sulfur cluster biogenesis in chloroplasts. Involvement of the scaffold protein CpIsca. Plant Physiol. 138: 161-172 (2005).
Ahmad A, Abraham G, Abdin MZ. Biochemical evaluation of sulfur and nitrogen assimilation potential of mustard (Brassica juncea L. Czern. & Coss.) under application of slow-release sulfur fertilizer. Appl. Biochem. Biotechnol. 96: 167-172 (2001).
Amir R, Hacham Y, Galili G. Cystathionine gamma-synthase and threonine synthase operate in concert to regulate carbon flow towards methionine in plants. Trends Plant Sci. 7: 153-157 (2002).
Awazuhara M, Fujiwara T, Hayashi H, Watanabe-Takahashi A, Takahashi H, Saito K. The function of SULTR2;1 sulfate transporter during seed development in Arabidopsis thaliana. Physiol. Plant. 125: 95-105 (2005).
Bagchi D, Verma D. Selenate-regulation of sulfur metabolism in a cyanobacterium, Phormidium uncinatum. J. Plant Physiol. 150: 762-764 (1997).
Ballere CL. Circadian maestro leads plant gene expression symphony. Trends Plant Sci. 6: 96-97 (2001).
Bell CI, Clarkson DT, Cram WJ. Partitioning and redistribution of sulfur during S-stress in Macroptilium atropurpureum cv Siratro. J. Exp. Bot. 46: 73-81 (1995).
Bick JA, Leustek T. Plant sulfur metabolism - the reduction of sulfate to sulfite. Curr. Opin. Plant Biol. 1: 240-244 (1998).
Binda C, Bossi RT, Wakatsuki S, Arzt S, Coda A, Curti B, Vanoni MA, Mattevi A. Cross-talk and ammonia channeling between active centers in the unexpected domain arrangement of glutamate synthase. Structure Fold. Des. 8: 1299-1308 (2000).
Blaszczyk A, Sirko L, Hawkesford MJ, Sirko A. Biochemical analysis of transgenic tobacco lines producing bacterial serine acetyltransferase. Plant Sci. 162: 589-597 (2002).
Bolchi A, Petrucco S, Tenca PL, Foroni C, Ottonello S. Coordinate modulation of maize sulfate permease and ATP sulfurylase mRNAs in response to variations in sulfur nutritional status: stereospecific down-regulation by L-cysteine. Plant Mol. Biol. 39: 527-537 (1999).
Borges-Walmsley MI, Turner G, Bailey AM, Brown J, Lehmbeck J, Clausen IG. Isolation and characterisation of genes for sulphate activation and reduction in Aspergillus nidulans: implications for evolution of an allosteric control region by gene duplication. Mol. Gen. Genet. 247: 423-429 (1995).
Brzywczy J, Sienko M, Kucharska A, Paszewski A. Sulphur amino acid synthesis in Schizosaccharomyces pombe represents a specific variant of sulphur metabolism in fungi. Yeast 19: 29-35 (2002).
Buchanan BB, Arnon DI. A reverse KREBS cycle in photosynthesis: consensus at last. Photosynth. Res. 24: 47-53 (1990).
Cherest H, Surdin-Kerjan Y. Genetic analysis of a new mutation conferring cysteine auxotrophy in Saccharomyces cerevisiae: updating of the sulfur metabolism pathway. Genetics 130: 51-58 (1992).
Chi-Ham CL, Keaton MA, Cannon GC, Heinhorst S. The DNA-compacting protein DCP68 from soybean chloroplasts is ferredoxin:sulfite reductase and co-localizes with the organellar nucleoid. Plant Mol. Biol. 49: 621-631 (2002).
Chiaiese P, Ohkama-Ohtsu N, Molvig L, Godfree R, Dove H, Hocart C, Fujiwara T, Higgins TJ, Tabe LM. Sulphur and nitrogen nutrition influence the response of chickpea seeds to an added, transgenic sink for organic sulphur. J. Exp. Bot. 55: 1889-1901 (2004).
Chronis D, Krishnan HB. Sulfur assimilation in soybean (Glycine max [L.] Merr.): molecular cloning and characterization of a cytosolic isoform of serine acetyltransferase. Planta 218: 417-426 (2004).
Coppee JY, Auger S, Turlin E, Sekowska A, Le Caer JP, Labas V, Vagner V, Danchin A, Martin-Verstraete I. Sulfur-limitation-regulated proteins in Bacillus subtilis: a two-dimensional gel electrophoresis study. Microbiology 147: 1631-1640 (2001).
Cumming M, Leung S, McCallum J, McManus MT. Complex formation between recombinant ATP sulfurylase and APS reductase of Allium cepa (L.). FEBS Lett. 581: 4139-4147 (2007).
Droux M. Sulfur assimilation and the role of sulfur in plant metabolism: a survey. Photosynth. Res. 79: 331-348 (2004).
Eilers T, Schwarz G, Brinkmann H, Witt C, Richter T, Nieder J, Koch B, Hille R, Hansch R, Mendel RR. Identification and biochemical characterization of Arabidopsis thaliana sulfite oxidase - A new player in plant sulfur metabolism. J. Biol. Chem. 276: 46989-46994 (2001).
Falk KL, Tokuhisa JG, Gershenzon J. The effect of sulfur nutrition on plant glucosinolate content: physiology and molecular mechanisms. Plant Biol. (Stuttg.) 9: 573-581 (2007).
Falkenberg B, Witt I, Zanor MI, Steinhauser D, Mueller-Roeber B, Hesse H, Hoefgen R. Transcription factors relevant to auxin signalling coordinate broad-spectrum metabolic shifts including sulphur metabolism. J. Exp. Bot. 59: 2831-2846 (2008).
Fauchon M, Lagniel G, Aude JC, Lombardia L, Soularue P, Petat C, Marguerie G, Sentenac A, Werner M, Labarre J. Sulfur sparing in the yeast proteome in response to sulfur demand. Mol. Cell 9: 713-723 (2002).
Ferreira S, Hjerno K, Larsen M, Wingsle G, Larsen P, Fey S, Roepstorff P, Salome Pais M. Proteome profiling of Populus euphratica Oliv. upon heat stress. Ann. Bot. (Lond.) 98: 361-377 (2006).
Freeman JL, Persans MW, Nieman K, Albrecht C, Peer W, Pickering IJ, Salt DE. Increased glutathione biosynthesis plays a role in nickel tolerance in thlaspi nickel hyperaccumulators. Plant Cell 16: 2176-2191 (2004).
Giordano M, Pezzoni V, Hell R. Strategies for the allocation of resources under sulfur limitation in the green alga Dunaliella salina. Plant Physiol. 124: 857-864 (2000).
Giovanelli J, Mudd SH, Datko AH. Homocysteine biosynthesis in green plants. Physiological importance of the transsulfuration pathway in Chlorella sorokiniana growing under steady state conditions with limiting sulfate. J. Biol. Chem. 253: 5665-5677 (1978).
Goffredi SK, Barry JP. Species-specific variation in sulfide physiology between closely related Vesicomyid clams. Mar. Ecol. Prog. Ser. 225: 227-238 (2002).
Gorbi G, Zanni C, Corradi MG. Sulfur starvation and chromium tolerance in Scenedesmus acutus: a possible link between metal tolerance and the regulation of sulfur uptake/assimilation processes. Aquat. Toxicol. 84: 457-464 (2007).
Hansen J, Johannesen PF. Cysteine is essential for transcriptional regulation of the sulfur assimilation genes in Saccharomyces cerevisiae. Mol. Gen. Genet. 263: 535-542 (2000).
Harada E, Kusano T, Sano H. Differential expression of genes encoding enzymes involved in sulfur assimilation pathways in response to wounding and jasmonate in Arabidopsis thaliana. J. Plant Physiol. 156: 272-276 (2000).
Hartmann T, Honicke P, Wirtz M, Hell R, Rennenberg H, Kopriva S. Regulation of sulphate assimilation by glutathione in poplars (Populus tremula x P. alba) of wild type and overexpressing gamma-glutamylcysteine synthetase in the cytosol. J. Exp. Bot. 55: 837-845 (2004).
Hartmann TN, Fricker MD, Rennenberg H, Meyer AJ. Cell-specific measurement of cytosolic glutathione in poplar leaves. Plant Cell Environ. 26: 965-975 (2003).
Hatzfeld Y, Cathala N, Grignon C, Davidian JC. Effect of ATP sulfurylase overexpression in bright yellow 2 tobacco cells. Regulation of ATP sulfurylase and SO4(2-) transport activities. Plant Physiol. 116: 1307-1313 (1998).
Hatzfeld Y, Lee S, Lee M, Leustek T, Saito K. Functional characterization of a gene encoding a fourth ATP sulfurylase isoform from Arabidopsis thaliana. Gene 248: 51-58 (2000).
Hawkesford MJ, De Kok LJ. Managing sulphur metabolism in plants. Plant Cell Environ. 29: 382-395 (2006).
Heiss S, Schafer HJ, Haag-Kerwer A, Rausch T. Cloning sulfur assimilation genes of Brassica juncea L.: cadmium differentially affects the expression of a putative low-affinity sulfate transporter and isoforms of ATP sulfurylase and APS reductase. Plant Mol. Biol. 39: 847-857 (1999).
Herschbach C, Mult S, Kreuzwieser J, Kopriva S. Influence of anoxia on whole plant sulphur nutrition of flooding-tolerant poplar (Populus tremula x P. alba). Plant Cell Environ. 28: 167-175 (2005).
Hoefgen R, Nikiforova VJ. Metabolomics integrated with transcriptomics: assessing systems response to sulfur-deficiency stress. Physiol. Plant. 132: 190-198 (2008).
Hofgen R, Kreft O, Willmitzer L, Hesse H. Manipulation of thiol contents in plants. Amino Acids 20: 291-299 (2001).
Hopkins L, Parmar S, Blaszczyk A, Hesse H, Hoefgen R, Hawkesford MJ. O-Acetylserine and the regulation of expression of genes encoding components for sulfate uptake and assimilation in potato. Plant Physiol. 138: 433-440 (2005).
Jost R, Altschmied L, Bloem E, Bogs J, Gershenzon J, Hahnel U, Hansch R, Hartmann T, Kopriva S, Kruse C, Mendel RR, Papenbrock J, Reichelt M, Rennenberg H, Schnug E, Schmidt A, Textor S, Tokuhisa J, Wachter A, Wirtz M, Rausch T, Hell R. Expression profiling of metabolic genes in response to methyl jasmonate reveals regulation of genes of primary and secondary sulfur-related pathways in Arabidopsis thaliana. Photosynth Res. 86: 491-508 (2005).
Kawashima CG, Berkowitz O, Hell R, Noji M, Saito K. Characterization and expression analysis of a serine acetyltransferase gene family involved in a key step of the sulfur assimilation pathway in Arabidopsis. Plant Physiol. 137: 220-230 (2005).
Kawashima CG, Yoshimoto N, Maruyama-Nakashita A, Tsuchiya YN, Saito K, Takahashi H, Dalmay T. Sulphur starvation induces the expression of microRNA-395 and one of its target genes but in different cell types. Plant J. 57: 313-321 (2009).
Keller MD, Kiene RP, Matrai PA, Bellows WK. Production of glycine betaine and dimethylsulfoniopropionate in marine phytoplankton. II. N-limited chemostat cultures. Mar. Biol. 135: 249-257 (1999).
Kiene RP, Linn LJ, Gonzalez J, Moran MA, Bruton JA. Dimethylsulfoniopropionate and methanethiol are important precursors of methionine and protein-sulfur in marine bacterioplankton. Appl. Environ. Microbiol. 65: 4549-4558 (1999).
Kim H, Hirai MY, Hayashi H, Chino M, Naito S, Fujiwara T. Role of O-acetyl-L-serine in the coordinated regulation of the expression of a soybean seed storage-protein gene by sulfur and nitrogen nutrition. Planta 209: 282-289 (1999).
Kopriva S. Regulation of sulfate assimilation in Arabidopsis and beyond. Ann. Bot. (Lond.) 97: 479-495 (2006).
Kopriva S, Buchert T, Fritz G, Suter M, Benda R, Schunemann V, Koprivova A, Schurmann P, Trautwein AX, Kroneck PM, Brunold C. The presence of an iron-sulfur cluster in adenosine 5'-phosphosulfate reductase separates organisms utilizing adenosine 5'-phosphosulfate and phosphoadenosine 5'-phosphosulfate for sulfate assimilation. J. Biol. Chem. 277: 21786-21791 (2002).
Kopriva S, Buchert T, Fritz G, Suter M, Weber M, Benda R, Schaller J, Feller U, Schurmann P, Schunemann V, Trautwein AX, Kroneck PM, Brunold C. Plant adenosine 5'-phosphosulfate reductase is a novel iron-sulfur protein. J. Biol. Chem. 276: 42881-42886 (2001).
Kopriva S, Koprivova A. Plant adenosine 5'-phosphosulphate reductase: the past, the present, and the future. J. Exp. Bot. 55: 1775-1783 (2004).
Kopriva S, Muheim R, Koprivova A, Trachsel N, Catalano C, Suter M, Brunold C. Light regulation of assimilatory sulphate reduction in Arabidopsis thaliana. Plant J. 20: 37-44 (1999).
Kopriva S, Rennenberg H. Control of sulphate assimilation and glutathione synthesis: interaction with N and C metabolism. J. Exp. Bot. 55: 1831-1842 (2004).
Kromer JO, Bolten CJ, Heinzle E, Schroder H, Wittmann C. Physiological response of Corynebacterium glutamicum to oxidative stress induced by deletion of the transcriptional repressor McbR. Microbiology 154: 3917-3930 (2008).
Kruse J, Kopriva S, Hansch R, Krauss GJ, Mendel RR, Rennenberg H. Interaction of sulfur and nitrogen nutrition in tobacco (Nicotiana tabacum) plants: significance of nitrogen source and root nitrate reductase. Plant Biol. (Stuttg.) 9: 638-646 (2007).
Kutz A, Muller A, Hennig P, Kaiser WM, Piotrowski M, Weiler EW. A role for nitrilase 3 in the regulation of root morphology in sulphur-starving Arabidopsis thaliana. Plant J. 30: 95-106 (2002).
Lappartient AG, Vidmar JJ, Leustek T, Glass AD, Touraine B. Inter-organ signaling in plants: regulation of ATP sulfurylase and sulfate transporter genes expression in roots mediated by phloem-translocated compound. Plant J. 18: 89-95 (1999).
Leustek T, Martin MN, Bick JA, Davies JP. Pathways and regulation of sulfur metabolism revealed through molecular and genetic studies. Annu. Rev. Plant Physiol. Plant Mol. Biol. 51: 141-165 (2000).
Leustek T, Murillo M, Cervantes M. Cloning of a cDNA encoding ATP sulfurylase from Arabidopsis thaliana by functional expression in Saccharomyces cerevisiae. Plant Physiol. 105: 897-902 (1994).
Lin JT, Stewart V. Nitrate assimilation by bacteria. Adv. Microbiol. Physiol. 39: 1-30 (1998).
Lunde C, Zygadlo A, Simonsen HT, Nielsen PL, Blennow A, Haldrup A. Sulfur starvation in rice: the effect on photosynthesis, carbohydrate metabolism, and oxidative stress protective pathways. Physiol. Plant. 134: 508-521 (2008).
Maruyama-Nakashita A, Inoue E, Watanabe-Takahashi A, Yamaya T, Takahashi H. Transcriptome profiling of sulfur-responsive genes in Arabidopsis reveals global effects of sulfur nutrition on multiple metabolic pathways. Plant Physiol. 132: 597-605 (2003).
Marzluf GA. Molecular genetics of sulfur assimilation in filamentous fungi and yeast. Annu. Rev. Microbiol. 51: 73-96 (1997).
McCallum JA, Pither-Joyce M, Shaw M. Sulfur deprivation and genotype affect gene expression and metabolism of onion roots. J. Am. Soc. Hortic. Sci. 127: 583-589 (2002).
Mendel RR, Bittner F. Cell biology of molybdenum. Biochim. Biophys. Acta 1763: 621-635 (2006).
Miyake T, Kanayama M, Sammoto H, Ono B. A novel cis-acting cysteine-responsive regulatory element of the gene for the high-affinity glutathione transporter of Saccharomyces cerevisiae. Mol. Genet. Genomics 266: 1004-1011 (2002).
Miyake T, Sammoto H, Kanayama M, Tomochika K, Shinoda S, Ono B. Role of the sulphate assimilation pathway in utilization of glutathione as a sulphur source by Saccharomyces cerevisiae. Yeast 15: 1449-1457 (1999).
Mo X, Marzluf GA. Cooperative action of the NIT2 and NIT4 transcription factors upon gene expression in Neurospora crassa. Curr. Genet. 42: 260-267 (2003).
Mosulen S, Dominguez MJ, Vigara J, Vilchez C, Guiraum A, Vega JM. Metal toxicity in Chlamydomonas reinhardtii. Effect on sulfate and nitrate assimilation. Biomol. Eng. 20: 199-203 (2003).
Murillo M, Foglia R, Diller A, Lee S, Leustek T. Serine acetyltransferase from Arabidopsis thaliana can functionally complement the cysteine requirement of a cysE mutant strain of Escherichia coli. Cell Mol. Biol. Res. 41: 425-433 (1995).
Murillo M, Leustek T. ATP-sulfurylase from Arabidopsis thaliana and Escherichia coli are functionally equivalent but structurally and kinetically divergent: nucleotide sequence of two ATP-sulfurylase cDNAs from Arabidopsis thaliana and analysis of a recombinant enzyme. Arch. Biochem. Biophys. 323: 195-204 (1995).
Nadolska-Lutyk J, Balinska M, Paszewski A. Interrelated regulation of sulphur-containing amino-acid biosynthetic enzymes and folate-metabolizing enzymes in Aspergillus nidulans. Eur. J. Biochem. 181: 231-235 (1989).
Nagasaka S, Takahashi M, Nakanishi-Itai R, Bashir K, Nakanishi H, Mori S, Nishizawa NK. Time course analysis of gene expression over 24 hours in Fe-deficient barley roots. Plant Mol. Biol. 69: 621-631 (2009).
Nikiforova V, Freitag J, Kempa S, Adamik M, Hesse H, Hoefgen R. Transcriptome analysis of sulfur depletion in Arabidopsis thaliana: interlacing of biosynthetic pathways provides response specificity. Plant J. 33: 633-650 (2003).
Nikiforova VJ, Kopka J, Tolstikov V, Fiehn O, Hopkins L, Hawkesford MJ, Hesse H, Hoefgen R. Systems rebalancing of metabolism in response to sulfur deprivation, as revealed by metabolome analysis of Arabidopsis plants. Plant Physiol. 138: 304-318 (2005).
Paszewski A, Ono BI. Biosynthesis of sulphur amino acids in Saccharomyces cerevisiae: regulatory roles of methionine and S-adenosylmethionine reassessed. Curr. Genet. 22: 273-275 (1992).
Paszewski A, Prazmo W, Nadolska J, Regulski M. Mutations affecting the sulphur assimilation pathway in Aspergillus nidulans: their effect on sulphur amino acid metabolism. J. Gen. Microbiol. 130: 1113-1121 (1984).
Petoukhov MV, Svergun DI, Konarev PV, Ravasio S, van den Heuvel RHH, Curti B, Vanoni MA. Quaternary structure of Azospirillum brasilense NADPH-dependent glutamate synthase in solution as revealed by synchrotron radiation x-ray scattering. J. Biol. Chem. 278: 29933-29939 (2003).
Phartiyal P, Kim WS, Cahoon RE, Jez JM, Krishnan HB. The role of 5'-adenylylsulfate reductase in the sulfur assimilation pathway of soybean: molecular cloning, kinetic characterization, and gene expression. Phytochemistry 69: 356-364 (2008).
Pilon-Smits EA, Hwang S, Mel Lytle C, Zhu Y, Tai JC, Bravo RC, Chen Y, Leustek T, Terry N. Overexpression of ATP sulfurylase in indian mustard leads to increased selenate uptake, reduction, and tolerance. Plant Physiol. 119: 123-132 (1999).
Pinto R, Harrison JS, Hsu T, Jacobs WR Jr, Leyh TS. Sulfite reduction in Mycobacteria. J. Bacteriol. 189: 6714-6722 (2007).
Prieto JL, Perez-Castineira JR, Vega JM. Thiosulfate reductase from Chlamydomonas. J. Plant Physiol. 151: 385-389 (1997).
Rausch T, Wachter A. Sulfur metabolism: a versatile platform for launching defence operations. Trends Plant Sci. 10: 503-509 (2005).
Rigano VDM, Vona V, Carfagna S, Esposito S, Carillo P, Rigano C. Effects of sulfate-starvation and re-supply on growth, NH4+ uptake and starch metabolism in Chlorella sorokiniana. Aust. J. Plant Physiol. 27: 335-342 (2000).
Rotte C, Leustek T. Differential subcellular localization and expression of ATP sulfurylase and 5'-adenylylsulfate reductase during ontogenesis of Arabidopsis leaves indicates that cytosolic and plastid forms of ATP sulfurylase may have specialized functions. Plant Physiol. 124: 715-724 (2000).
Ruelland E, Miginiac-Maslow M. Regulation of chloroplast enzyme activities by thioredoxins: activation or relief from inhibition? Trends Plant Sci. 4: 136-141 (1999).
Saito K. Regulation of sulfate transport and synthesis of sulfur-containing amino acids. Curr. Opin. Plant Biol. 3: 188-195 (2000).
Saito K, Miura N, Yamazaki M, Hirano H, Murakoshi I. Molecular cloning and bacterial expression of cDNA encoding a plant cysteine synthase. Proc. Natl. Acad. Sci. U.S.A. 89: 8078-8082 (1992).
Salome PA, Michael TP, Kearns EV, Fett-Neto AG, Sharrock RA, McClung CR. The out of phase 1 mutant defines a role for PHYB in circadian phase control in Arabidopsis. Plant Physiol. 129: 1674-1685 (2002).
Schwarz G, Mendel RR. Molybdenum cofactor biosynthesis and molybdenum enzymes. Annu. Rev. Plant Biol. 57: 623-647 (2006).
Shakoury-Elizeh M, Tiedeman J, Rashford J, Ferea T, Demeter J, Garcia E, Rolfes R, Brown PO, Botstein D, Philpott CC. Transcriptional remodeling in response to iron deprivation in Saccharomyces cerevisiae. Mol. Biol. Cell 15: 1233-1243 (2004).
Sharma N, Cram D, Huebert T, Zhou N, Parkin IA. Exploiting the wild crucifer Thlaspi arvense to identify conserved and novel genes expressed during a plant's response to cold stress. Plant Mol. Biol. 63: 171-184 (2007).
Sohn H, Kuriyama H. Ultradian metabolic oscillation of Saccharomyces cerevisiae during aerobic continuous culture: hydrogen sulphide, a population synchronizer, is produced by sulphite reductase. Yeast 18: 125-135 (2001).
Sohn H, Kuriyama H. The role of amino acids in the regulation of hydrogen sulfide production during ultradian respiratory oscillation of Saccharomyces cerevisiae. Arch. Microbiol. 176: 69-78 (2001).
Sors TG, Ellis DR, Na GN, Lahner B, Lee S, Leustek T, Pickering IJ, Salt DE. Analysis of sulfur and selenium assimilation in Astragalus plants with varying capacities to accumulate selenium. Plant J. 42: 785-797 (2005).
Stuiver CEE, DeKok LJ, Westerman S. Sulfur deficiency in Brassica oleracea L: Development, biochemical characterization, and sulfur/nitrogen interactions. Russ. J. Plant Physiol. 44: 505-513 (1997).
Swamy U, Wang M, Tripathy JN, Kim SK, Hirasawa M, Knaff DB, Allen JP. Structure of spinach nitrite reductase: implications for multi-electron reactions by the iron-sulfur:siroheme cofactor. Biochemistry 44: 16054-16063 (2005).
Tabe LM, Droux M. Sulfur assimilation in developing lupin cotyledons could contribute significantly to the accumulation of organic sulfur reserves in the seed. Plant Physiol. 126: 176-187 (2001).
Takagi H, Yoshioka K, Awano N, Nakamori S, Ono B. Role of Saccharomyces cerevisiae serine O-acetyltransferase in cysteine biosynthesis. FEMS Microbiol. Lett. 218: 291-297 (2003).
Takahashi H, Yamazaki M, Sasakura N, Watanabe A, Leustek T, Engler JA, Engler G, Van Montagu M, Saito K. Regulation of sulfur assimilation in higher plants: a sulfate transporter induced in sulfate-starved roots plays a central role in Arabidopsis thaliana. Proc. Natl. Acad. Sci. U.S.A. 94: 11102-11107 (1997).
Terry N, Zayed AM, de Souza MP, Tarun AS. Selenium in higher plants. Annu. Rev. Plant Physiol. Plant Mol. Biol. 51: 401-432 (2000).
Thomas D, Kuras L, Barbey R, Cherest H, Blaiseau PL, Surdin-Kerjan Y. Met30p, a yeast transcriptional inhibitor that responds to S-adenosylmethionine, is an essential protein with WD40 repeats. Mol. Cell Biol. 15: 6526-6534 (1995).
Thomas D, Surdin-Kerjan Y. Metabolism of sulfur amino acids in Saccharomyces cerevisiae. Microbiol. Mol. Biol. Rev. 61: 503-532 (1997).
Uria-Nickelsen MR, Leadbetter ER, Godchaux W 3d. Sulfonate-sulfur assimilation by yeasts resembles that of bacteria. FEMS Microbiol. Lett. 114: 73-77 (1993).
van der Ploeg JR, Eichhorn E, Leisinger T. Sulfonate-sulfur metabolism and its regulation in Escherichia coli. Arch. Microbiol. 176: 1-8 (2001).
Van Hoewyk D, Abdel-Ghany SE, Cohu CM, Herbert SK, Kugrens P, Pilon M, Pilon-Smits EA. Chloroplast iron-sulfur cluster protein maturation requires the essential cysteine desulfurase CpNifS. Proc. Natl. Acad. Sci. U.S.A. 104: 5686-5691 (2007).
Vanoni MA, Curti B. Structure-function studies on the iron-sulfur flavoenzyme glutamate synthase: an unexpectedly complex self-regulated enzyme. Arch. Biochem. Biophys. 433: 193-211 (2005).
Vanoni MA, Curti B. Glutamate synthase: a complex iron-sulfur flavoprotein. Cell Mol. Life Sci. 55: 617-638 (1999).
Vanoni MA, Curti B. Structure-function studies of glutamate synthases: a class of self-regulated iron-sulfur flavoenzymes essential for nitrogen assimilation. IUBMB Life 60: 287-300 (2008).
Vanoni MA, Dossena L, van den Heuvel RH, Curti B. Structure-function studies on the complex iron-sulfur flavoprotein glutamate synthase: the key enzyme of ammonia assimilation. Photosynth. Res. 83: 219-238 (2005).
Vauclare P, Kopriva S, Fell D, Suter M, Sticher L, von Ballmoos P, Krahenbuhl U, den Camp RO, Brunold C. Flux control of sulphate assimilation in Arabidopsis thaliana: adenosine 5'-phosphosulphate reductase is more susceptible than ATP sulphurylase to negative control by thiols. Plant J. 31: 729-740 (2002).
Vermeij P, Kertesz MA. Pathways of assimilative sulfur metabolism in Pseudomonas putida. J. Bacteriol. 181: 5833-5837 (1999).
Watanabe M, Mochida K, Kato T, Tabata S, Yoshimoto N, Noji M, Saito K. Comparative genomics and reverse genetics analysis reveal indispensable functions of the serine acetyltransferase gene family in Arabidopsis. Plant Cell 20: 2484-2496 (2008).
Weber AP, Schwacke R, Flugge UI. Solute transporters of the plastid envelope membrane. Annu. Rev. Plant Biol. 56: 133-164 (2005).
White PJ, Bowen HC, Parmaguru P, Fritz M, Spracklen WP, Spiby RE, Meacham MC, Mead A, Harriman M, Trueman LJ, Smith BM, Thomas B, Broadley MR. Interactions between selenium and sulphur nutrition in Arabidopsis thaliana. J. Exp. Bot. 55: 1927-1937 (2004).
Wiedemann G, Koprivova A, Schneider M, Herschbach C, Reski R, Kopriva S. The role of the novel adenosine 5'-phosphosulfate reductase in regulation of sulfate assimilation of Physcomitrella patens. Plant Mol. Biol. 65: 667-676 (2007).
Wirtz M, Droux M, Hell R. O-Acetylserine (thiol) lyase: an enigmatic enzyme of plant cysteine biosynthesis revisited in Arabidopsis thaliana. J. Exp. Bot. 55: 1785-1798 (2004).
Zdunek-Zastocka E, Lips HS. Plant molybdoenzymes and their response to stress. Acta Physiol. Plant. 25: 437-452 (2003).
Number of references = 120
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