Sulfur amino acid metabolism: pathways for production and removal of homocysteine and cysteine.

Tissue concentrations of both homocysteine (Hcy) and cysteine (Cys) are maintained at low levels by regulated production and efficient removal of these thiols. The regulation of the metabolism of methionine and Cys is discussed from the standpoint of maintaining low levels of Hcy and Cys while, at the same time, ensuring an adequate supply of these thiols for their essential functions. S-Adenosylmethionine coordinately regulates the flux through remethylation and transsulfuration, and glycine N-methyltransferase regulates flux through transmethylation and hence the S-adenosylmethionine/S-adenosylhomocysteine ratio. Cystathionine beta-synthase activity is also regulated in response to the redox environment, and transcription of the gene is hormonally regulated in response to fuel supply (insulin, glucagon, and glucocorticoids). The H2S-producing capacity of cystathionine gamma-lyase may be regulated in response to nitric oxide. Cys is substrate for a variety of anabolic and catabolic enzymes. Its concentration is regulated primarily by hepatic Cys dioxygenase; the level of Cys dioxygenase is upregulated in a Cys-responsive manner via a decrease in the rate of polyubiquitination and, hence, degradation by the 26S proteasome.

[1]  M. Watanabe,et al.  Expression and localization of cysteine dioxygenase mRNA in the liver, lung, and kidney of the rat , 2005, Amino Acids.

[2]  R. Chamuleau,et al.  Changes in urinary taurine and hypotaurine excretion after two-thirds hepatectomy in the rat , 2005, Amino Acids.

[3]  J. Gregory,et al.  Folate deprivation reduces homocysteine remethylation in a human intestinal epithelial cell culture model: role of serine in one-carbon donation. , 2004, American journal of physiology. Gastrointestinal and liver physiology.

[4]  M. Stipanuk,et al.  The ubiquitin-proteasome system is responsible for cysteine-responsive regulation of cysteine dioxygenase concentration in liver. , 2004, American journal of physiology. Endocrinology and metabolism.

[5]  M. Stipanuk,et al.  Regulation of cysteine dioxygenase and gamma-glutamylcysteine synthetase is associated with hepatic cysteine level. , 2004, The Journal of nutritional biochemistry.

[6]  L. Bailey,et al.  Tracer-derived total and folate-dependent homocysteine remethylation and synthesis rates in humans indicate that serine is the main one-carbon donor. , 2004, American journal of physiology. Endocrinology and metabolism.

[7]  R. Lorini,et al.  Glycine N-methyltransferase deficiency: A novel inborn error causing persistent isolated hypermethioninaemia , 2001, Journal of Inherited Metabolic Disease.

[8]  M. Durán,et al.  Dietary therapy in two patients with a mild form of sulphite oxidase deficiency. Evidence for clinical and biological improvement , 2000, Journal of Inherited Metabolic Disease.

[9]  K. Rajagopalan,et al.  An HPLC assay for detection of elevated urinaryS-sulphocysteine, a metabolic marker of sulphite oxidase deficiency , 1995, Journal of Inherited Metabolic Disease.

[10]  D. Thiel,et al.  Evidence for expression of a single distinct form of mammalian cysteine dioxygenase , 2004, Amino Acids.

[11]  H. Osswald,et al.  Adenosine binding sites at S-adenosylhomocysteine hydrolase are controlled by the NAD+/NADH ratio of the enzyme. , 2003, Biochemical pharmacology.

[12]  K. Schalinske,et al.  Retinoic acid and glucocorticoid treatment induce hepatic glycine N-methyltransferase and lower plasma homocysteine concentrations in rats and rat hepatoma cells. , 2003, The Journal of nutrition.

[13]  M. Stipanuk,et al.  Cysteine is the metabolic signal responsible for dietary regulation of hepatic cysteine dioxygenase and glutamate cysteine ligase in intact rats. , 2003, The Journal of nutrition.

[14]  J. Zvárová,et al.  Genetic variants of homocysteine metabolizing enzymes and the risk of coronary artery disease. , 2003, Molecular genetics and metabolism.

[15]  Yafei Huang,et al.  Catalytic mechanism of glycine N-methyltransferase. , 2003, Biochemistry.

[16]  S. Oltean,et al.  Nutritional Modulation of Gene Expression and Homocysteine Utilization by Vitamin B12* , 2003, Journal of Biological Chemistry.

[17]  N. Sakura,et al.  Limited effectiveness of betaine therapy for cystathionine β synthase deficiency , 2003, Pediatrics international : official journal of the Japan Pediatric Society.

[18]  R. Banerjee,et al.  Tumor Necrosis Factor-α-induced Targeted Proteolysis of Cystathionine β-Synthase Modulates Redox Homeostasis* , 2003, The Journal of Biological Chemistry.

[19]  J. Finkelstein,et al.  Methionine metabolism in liver diseases. , 2003, The American journal of clinical nutrition.

[20]  S. Zeisel,et al.  Concentrations of choline-containing compounds and betaine in common foods. , 2003, The Journal of nutrition.

[21]  Y. C. Kim,et al.  Effect of acute betaine administration on hepatic metabolism of S-amino acids in rats and mice. , 2003, Biochemical pharmacology.

[22]  H. Brown-Borg,et al.  Altered methionine metabolism in long living Ames dwarf mice , 2003, Experimental Gerontology.

[23]  S. J. James,et al.  Cobalamin deficiency with and without neurologic abnormalities: differences in homocysteine and methionine metabolism. , 2003, Blood.

[24]  S. Ojha,et al.  Reaction mechanism and regulation of cystathionine β-synthase , 2003 .

[25]  H. McNulty,et al.  Genetic and nutritional factors contributing to hyperhomocysteinemia in young adults. , 2003, Blood.

[26]  B. Otlu,et al.  Effects of valproate and carbamazepine on serum levels of homocysteine, vitamin B12, and folic acid , 2003, Brain and Development.

[27]  K. Robert,et al.  Expression of the Cystathionine β Synthase (CBS) Gene During Mouse Development and Immunolocalization in Adult Brain , 2003, The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society.

[28]  D. Cole,et al.  Regulation of sulfur amino acid metabolism in men in response to changes in sulfur amino acid intakes. , 2003, The Journal of nutrition.

[29]  R. Hegele,et al.  Genomic basis of cystathioninuria (MIM 219500) revealed by multiple mutations in cystathionine gamma-lyase (CTH) , 2003, Human Genetics.

[30]  E. Mosharov,et al.  Redox regulation of homocysteine-dependent glutathione synthesis , 2003, Redox report : communications in free radical research.

[31]  O. Park,et al.  Effects of cysteine on amino acid concentrations and transsulfuration enzyme activities in rat liver with protein-calorie malnutrition. , 2003, Life sciences.

[32]  S. Vollset,et al.  Plasma total cysteine, pregnancy complications, and adverse pregnancy outcomes: the Hordaland Homocysteine Study. , 2000, The American journal of clinical nutrition.

[33]  M. Rainfray,et al.  Prevalence and mechanisms of hyperhomocysteinemia in elderly hospitalized patients. , 2003, The journal of nutrition, health & aging.

[34]  J. Kraus,et al.  Deletion mutagenesis of human cystathionine beta-synthase. Impact on activity, oligomeric status, and S-adenosylmethionine regulation. , 2002, The Journal of biological chemistry.

[35]  M. Brosnan,et al.  Hormonal Regulation of Cystathionine β-Synthase Expression in Liver* , 2002, The Journal of Biological Chemistry.

[36]  K. Eto,et al.  A Novel Enhancing Mechanism for Hydrogen Sulfide-producing Activity of Cystathionine β-Synthase* , 2002, The Journal of Biological Chemistry.

[37]  Dean P. Jones,et al.  Redox analysis of human plasma allows separation of pro-oxidant events of aging from decline in antioxidant defenses. , 2002, Free radical biology & medicine.

[38]  M. Stipanuk,et al.  Enzymes and metabolites of cysteine metabolism in nonhepatic tissues of rats show little response to changes in dietary protein or sulfur amino acid levels. , 2002, The Journal of nutrition.

[39]  R. Banerjee,et al.  Differences in the efficiency of reductive activation of methionine synthase and exogenous electron acceptors between the common polymorphic variants of human methionine synthase reductase. , 2002, Biochemistry.

[40]  M. Kushiro,et al.  mRNA expression of enzymes involved in taurine biosynthesis in rat adipose tissues. , 2002, Metabolism: clinical and experimental.

[41]  J. C. Evans,et al.  Betaine-homocysteine methyltransferase: zinc in a distorted barrel. , 2002, Structure.

[42]  P. K. Moore,et al.  The smooth muscle relaxant effect of hydrogen sulphide in vitro: evidence for a physiological role to control intestinal contractility , 2002, British journal of pharmacology.

[43]  David C Chipman,et al.  Hepatic glycine N-methyltransferase is up-regulated by excess dietary methionine in rats. , 2002, The Journal of nutrition.

[44]  N. Gordon Pantothenate kinase-associated neurodegeneration (Hallervorden-Spatz syndrome). , 2002, European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.

[45]  Rui Wang,et al.  H2S-induced vasorelaxation and underlying cellular and molecular mechanisms , 2002 .

[46]  C. Steegborn,et al.  Elevated plasma total homocysteine in severe methionine adenosyltransferase I/III deficiency. , 2002, Metabolism: clinical and experimental.

[47]  N. Sakura,et al.  Betaine and homocysteine concentrations in foods , 2002, Pediatrics international : official journal of the Japan Pediatric Society.

[48]  Sang-Woon Choi,et al.  In the cystathionine beta-synthase knockout mouse, elevations in total plasma homocysteine increase tissue S-adenosylhomocysteine, but responses of S-adenosylmethionine and DNA methylation are tissue specific. , 2002, The Journal of nutrition.

[49]  Shelly C. Lu,et al.  Spontaneous oxidative stress and liver tumors in mice lacking methionine adenosyltransferase 1A , 2002, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.

[50]  Dagmar Ringe,et al.  Human cystathionine beta-synthase is a heme sensor protein. Evidence that the redox sensor is heme and not the vicinal cysteines in the CXXC motif seen in the crystal structure of the truncated enzyme. , 2002, Biochemistry.

[51]  R. Borchardt,et al.  Contributions of active site residues to the partial and overall catalytic activities of human S-adenosylhomocysteine hydrolase. , 2002, Biochemistry.

[52]  T. Asada,et al.  Brain hydrogen sulfide is severely decreased in Alzheimer's disease. , 2002, Biochemical and biophysical research communications.

[53]  H. Canatan,et al.  Insulin increases homocysteine levels in a dose-dependent manner in diabetic rats. , 2002, Archives of medical research.

[54]  Y. Nagai,et al.  Hydrogen Sulfide Is Produced in Response to Neuronal Excitation , 2002, The Journal of Neuroscience.

[55]  Y. Ozkan,et al.  Plasma total homocysteine and cysteine levels as cardiovascular risk factors in coronary heart disease. , 2002, International journal of cardiology.

[56]  K. Schalinske,et al.  Vitamin A and its derivatives induce hepatic glycine N-methyltransferase and hypomethylation of DNA in rats. , 2002, The Journal of nutrition.

[57]  M. Pomper,et al.  Progressive cerebral edema associated with high methionine levels and betaine therapy in a patient with cystathionine beta-synthase (CBS) deficiency. , 2002, American journal of medical genetics.

[58]  A. Nicolaou,et al.  Methionine synthase activity and sulphur amino acid levels in the rat liver tumour cells HTC and Phi-1. , 2002, Biochemical pharmacology.

[59]  Y. Kwon,et al.  Cysteine metabolism in periportal and perivenous hepatocytes: Perivenous cells have greater capacity for glutathione production and taurine synthesis but not for cysteine catabolism , 2002, Amino Acids.

[60]  R. Kajikawa,et al.  A study on the estimation of sulfur-containing amino acid metabolism by the determination of urinary sulfate and taurine , 2002, Amino Acids.

[61]  M. Aschner,et al.  Identification and characterization of uptake systems for cystine and cysteine in cultured astrocytes and neurons: Evidence for methylmercury‐targeted disruption of astrocyte transport , 2001, Journal of neuroscience research.

[62]  R. Ball,et al.  Dietary cysteine reduces the methionine requirement in men. , 2001, The American journal of clinical nutrition.

[63]  R. Ball,et al.  Total sulfur amino acid requirement in young men as determined by indicator amino acid oxidation with L-[1-13C]phenylalanine. , 2001, The American journal of clinical nutrition.

[64]  M. Brosnan,et al.  Hyperglucagonemia in Rats Results in Decreased Plasma Homocysteine and Increased Flux through the Transsulfuration Pathway in Liver* , 2001, The Journal of Biological Chemistry.

[65]  Rui Wang,et al.  The vasorelaxant effect of H2S as a novel endogenous gaseous KATP channel opener , 2001 .

[66]  G. McBean,et al.  Molecular mechanisms of cystine transport. , 2001, Biochemical Society transactions.

[67]  M. Stipanuk,et al.  Murine cysteine dioxygenase gene: structural organization, tissue-specific expression and promoter identification. , 2001, Gene.

[68]  M. Gaustadnes,et al.  Regulation of human cystathionine beta-synthase by S-adenosyl-L-methionine: evidence for two catalytically active conformations involving an autoinhibitory domain in the C-terminal region. , 2001, Biochemistry.

[69]  C. Stehouwer,et al.  Homocysteine-lowering treatment: an overview , 2001, Expert opinion on pharmacotherapy.

[70]  T. Garrow,et al.  Immunohistochemical detection of betaine-homocysteine S-methyltransferase in human, pig, and rat liver and kidney. , 2001, Archives of biochemistry and biophysics.

[71]  P Burkhard,et al.  Structure of human cystathionine β‐synthase: a unique pyridoxal 5′‐phosphate‐dependent heme protein , 2001, The EMBO journal.

[72]  Shawn K. Westaway,et al.  A novel pantothenate kinase gene (PANK2) is defective in Hallervorden-Spatz syndrome , 2001, Nature Genetics.

[73]  M. Kotb,et al.  Regulation of the Human MAT2B Gene Encoding the Regulatory β Subunit of Methionine Adenosyltransferase, MAT II* , 2001, The Journal of Biological Chemistry.

[74]  I. Pogribny,et al.  Homocysteine metabolism in children with Down syndrome: in vitro modulation. , 2001, American journal of human genetics.

[75]  N. Maeda,et al.  Endothelial Dysfunction and Elevation of S-Adenosylhomocysteine in Cystathionine &bgr;-Synthase–Deficient Mice , 2001, Circulation research.

[76]  R. Banerjee,et al.  Pyridoxal phosphate binding sites are similar in human heme-dependent and yeast heme-independent cystathionine beta-synthases. Evidence from 31P NMR and pulsed EPR spectroscopy that heme and PLP cofactors are not proximal in the human enzyme. , 2001, The Journal of biological chemistry.

[77]  S. Vollset,et al.  Plasma Total Cysteine as a Risk Factor for Vascular Disease: The European Concerted Action Project , 2001, Circulation.

[78]  Shelly C. Lu,et al.  Methionine adenosyltransferase 1A knockout mice are predisposed to liver injury and exhibit increased expression of genes involved in proliferation , 2001, Proceedings of the National Academy of Sciences of the United States of America.

[79]  Manisha Singh,et al.  L‐Cysteine and Sodium Hydrosulphide Inhibit Spontaneous Contractility in Isolated Pregnant Rat Uterine Strips in vitro , 2001 .

[80]  Roland L. Dunbrack,et al.  Mutations in the regulatory domain of cystathionine beta synthase can functionally suppress patient-derived mutations in cis. , 2001, Human molecular genetics.

[81]  M. Rudnicki,et al.  Mice deficient in methylenetetrahydrofolate reductase exhibit hyperhomocysteinemia and decreased methylation capacity, with neuropathology and aortic lipid deposition. , 2001, Human molecular genetics.

[82]  C. Masters,et al.  Homocysteine potentiates copper‐ and amyloid beta peptide‐mediated toxicity in primary neuronal cultures: possible risk factors in the Alzheimer's‐type neurodegenerative pathways , 2001, Journal of neurochemistry.

[83]  J. B. Park Reduction of dehydroascorbic acid by homocysteine. , 2001, Biochimica et biophysica acta.

[84]  M. Stitzel,et al.  Targeted Disruption of the Methionine Synthase Gene in Mice , 2001, Molecular and Cellular Biology.

[85]  M. Palacín,et al.  The amino acid transport system bo,+ and cystinuria , 2001, Molecular membrane biology.

[86]  J. Toth,et al.  Primed, constant infusion with [2H3]serine allows in vivo kinetic measurement of serine turnover, homocysteine remethylation, and transsulfuration processes in human one-carbon metabolism. , 2000, The American journal of clinical nutrition.

[87]  J. Nadeau,et al.  Betaine-homocysteine methyltransferase-2: cDNA cloning, gene sequence, physical mapping, and expression of the human and mouse genes. , 2000, Genomics.

[88]  E. Mosharov,et al.  The quantitatively important relationship between homocysteine metabolism and glutathione synthesis by the transsulfuration pathway and its regulation by redox changes. , 2000, Biochemistry.

[89]  F I Ataullakhanov,et al.  A substrate switch: a new mode of regulation in the methionine metabolic pathway. , 2000, Journal of theoretical biology.

[90]  Y. M. Chen,et al.  Genomic structure, expression, and chromosomal localization of the human glycine N-methyltransferase gene. , 2000, Genomics.

[91]  Dean P. Jones,et al.  Redox state of glutathione in human plasma. , 2000, Free radical biology & medicine.

[92]  J. Chou,et al.  Methionine adenosyltransferase I/III deficiency: novel mutations and clinical variations. , 2000, American journal of human genetics.

[93]  M. Regan,et al.  Cysteine kinetics and oxidation at different intakes of methionine and cystine in young adults. , 2000, The American journal of clinical nutrition.

[94]  H. Kimura Hydrogen sulfide induces cyclic AMP and modulates the NMDA receptor. , 2000, Biochemical and biophysical research communications.

[95]  J. Finkelstein,et al.  Pathways and Regulation of Homocysteine Metabolism in Mammals , 2000, Seminars in thrombosis and hemostasis.

[96]  Y. Kwon,et al.  Post-transcriptional regulation of cysteine dioxygenase in rat liver. , 2000, Advances in experimental medicine and biology.

[97]  R. Rozen Genetic Modulation of Homocysteinemia , 2000, Seminars in thrombosis and hemostasis.

[98]  J. Chou Molecular genetics of hepatic methionine adenosyltransferase deficiency. , 2000, Pharmacology & therapeutics.

[99]  C. Wagner,et al.  Inhibition of Glycine N-Methyltransferase by 5-Methyltetrahydrofolate Pentaglutamate* , 1999, The Journal of Biological Chemistry.

[100]  S. Vollset,et al.  Lifestyle and cardiovascular disease risk factors as determinants of total cysteine in plasma: the Hordaland Homocysteine Study. , 1999, The American journal of clinical nutrition.

[101]  R. Banerjee,et al.  Assignment of enzymatic functions to specific regions of the PLP-dependent heme protein cystathionine beta-synthase. , 1999, Biochemistry.

[102]  A. Breksa,et al.  Recombinant human liver betaine-homocysteine S-methyltransferase: identification of three cysteine residues critical for zinc binding. , 1999, Biochemistry.

[103]  A. Donker,et al.  Homocysteine and methionine metabolism in ESRD: A stable isotope study. , 1999, Kidney international.

[104]  Y. Ravindranath,et al.  Expression of chromosome 21-localized genes in acute myeloid leukemia: differences between Down syndrome and non-Down syndrome blast cells and relationship to in vitro sensitivity to cytosine arabinoside and daunorubicin. , 1999, Blood.

[105]  Eiji Takeda,et al.  Identification and Functional Characterization of a Na+-independent Neutral Amino Acid Transporter with Broad Substrate Selectivity* , 1999, The Journal of Biological Chemistry.

[106]  M. Brosnan,et al.  Regulation of homocysteine metabolism. , 1999, Advances in enzyme regulation.

[107]  T. Garrow,et al.  Interaction between Dietary Methionine and Methyl Donor Intake on Rat Liver Betaine-homocysteine Methyltransferase Gene Expression and Organization of the Human Gene* , 1999, The Journal of Biological Chemistry.

[108]  G. Varela-Moreiras,et al.  Impaired methionine synthesis and hypomethylation in rats exposed to valproate during gestation , 1999, Neurology.

[109]  P. Kamoun,et al.  Spatial and temporal expression of the cystathionine beta-synthase gene during early human development. , 1999, Biochemical and biophysical research communications.

[110]  M. Brosnan,et al.  Effects of streptozotocin-induced diabetes and of insulin treatment on homocysteine metabolism in the rat. , 1998, Diabetes.

[111]  R Clarke,et al.  Folate, vitamin B12, and serum total homocysteine levels in confirmed Alzheimer disease. , 1998, Archives of neurology.

[112]  L. Shantz,et al.  S-adenosylmethionine decarboxylase: structure, function and regulation by polyamines. , 1998, Biochemical Society transactions.

[113]  R. Banerjee,et al.  Evidence for Heme-mediated Redox Regulation of Human Cystathionine β-Synthase Activity* , 1998, The Journal of Biological Chemistry.

[114]  J. Finkelstein,et al.  Methionine-sparing effect of cystine in human subjects. , 1998, The American journal of clinical nutrition.

[115]  N. Fukagawa,et al.  Methionine and cysteine kinetics at different intakes of methionine and cysteine in elderly men and women. , 1998, The American journal of clinical nutrition.

[116]  D. Leibfritz,et al.  Metabolism of Cysteine in Astroglial Cells: Synthesis of Hypotaurine and Taurine , 1998, Journal of neurochemistry.

[117]  P. O'Brien,et al.  The glutathione dependence of inorganic sulfate formation from L- or D-cysteine in isolated rat hepatocytes. , 1998, Chemico-biological interactions.

[118]  T. Ubuka,et al.  Excretion of sulfate and taurine in rats fed with a high protein diet. , 1998, Acta medica Okayama.

[119]  T. Ubuka,et al.  Excretion of taurine and sulfate in rats fed with a low protein diet. , 1998, Acta medica Okayama.

[120]  J. Saudubray,et al.  Remethylation defects: guidelines for clinical diagnosis and treatment , 1998, European Journal of Pediatrics.

[121]  J. Till,et al.  Strategies for the treatment of cystathionine β-synthase deficiency: the experience of the Willink Biochemical Genetics Unit over the past 30 years , 1998, European Journal of Pediatrics.

[122]  D. Rees,et al.  Molecular Basis of Sulfite Oxidase Deficiency from the Structure of Sulfite Oxidase , 1997, Cell.

[123]  J. Lindemans,et al.  Methionine synthase deficiency without megaloblastic anaemia , 1997, European Journal of Pediatrics.

[124]  T. Garrow,et al.  Diet-induced changes in hepatic betaine-homocysteine methyltransferase activity are mediated by changes in the steady-state level of its mRNA , 1997 .

[125]  S. Sunden,et al.  Betaine-homocysteine methyltransferase expression in porcine and human tissues and chromosomal localization of the human gene. , 1997, Archives of biochemistry and biophysics.

[126]  N. Matsuki,et al.  The possible role of hydrogen sulfide as an endogenous smooth muscle relaxant in synergy with nitric oxide. , 1997, Biochemical and biophysical research communications.

[127]  J. Witteman,et al.  Plasma homocysteine as a risk factor for vascular disease. The European Concerted Action Project. , 1997, JAMA.

[128]  D. Ramsay,et al.  Isolated sulfite oxidase deficiency. , 1996, Neuropediatrics.

[129]  T. Koide,et al.  Structural organization and tissue-specific expression of the gene encoding rat cysteine dioxygenase. , 1996, Gene.

[130]  S. Vollset,et al.  Determinants and vitamin responsiveness of intermediate hyperhomocysteinemia (> or = 40 micromol/liter). The Hordaland Homocysteine Study. , 1996, The Journal of clinical investigation.

[131]  Y. Kwon,et al.  Variations in dietary protein but not in dietary fat plus cellulose or carbohydrate levels affect cysteine metabolism in rat isolated hepatocytes. , 1996, The Journal of nutrition.

[132]  W. Vermaak,et al.  The effect of a subnormal vitamin B-6 status on homocysteine metabolism. , 1996, The Journal of clinical investigation.

[133]  K. Abe,et al.  The possible role of hydrogen sulfide as an endogenous neuromodulator , 1996, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[134]  P. Jungers,et al.  Long-term folic acid (but not pyridoxine) supplementation lowers elevated plasma homocysteine level in chronic renal failure. , 1996, Mineral and electrolyte metabolism.

[135]  I. Rosenberg,et al.  Relation between folate status, a common mutation in methylenetetrahydrofolate reductase, and plasma homocysteine concentrations. , 1996, Circulation.

[136]  J. Chou,et al.  Molecular mechanisms of an inborn error of methionine pathway. Methionine adenosyltransferase deficiency. , 1995, The Journal of clinical investigation.

[137]  J. Brosnan,et al.  Net uptake of plasma homocysteine by the rat kidney in vivo. , 1995, Atherosclerosis.

[138]  R. Waring,et al.  Sulphoxidation and sulphation capacity in patients with primary biliary cirrhosis. , 1995, Journal of hepatology.

[139]  M. Stipanuk,et al.  Evaluation and modification of an assay procedure for cysteine dioxygenase activity: high-performance liquid chromatography method for measurement of cysteine sulfinate and demonstration of physiological relevance of cysteine dioxygenase activity in cysteine catabolism. , 1995, Analytical biochemistry.

[140]  M. Stipanuk,et al.  Rats fed a low protein diet supplemented with sulfur amino acids have increased cysteine dioxygenase activity and increased taurine production in hepatocytes. , 1995, The Journal of nutrition.

[141]  N. Maeda,et al.  Mice deficient in cystathionine beta-synthase: animal models for mild and severe homocyst(e)inemia. , 1995, Proceedings of the National Academy of Sciences of the United States of America.

[142]  H. Blom,et al.  Thermolabile 5,10-methylenetetrahydrofolate reductase as a cause of mild hyperhomocysteinemia. , 1995, American journal of human genetics.

[143]  M. Stipanuk,et al.  The activities of rat hepatic cysteine dioxygenase and cysteinesulfinate decarboxylase are regulated in a reciprocal manner in response to dietary casein level. , 1994, The Journal of nutrition.

[144]  W. Vermaak,et al.  Vitamin requirements for the treatment of hyperhomocysteinemia in humans. , 1994, The Journal of nutrition.

[145]  J. Paauw,et al.  Taurine supplementation at three different dosages and its effect on trauma patients. , 1994, The American journal of clinical nutrition.

[146]  P. Emery,et al.  Sulfate metabolism is abnormal in patients with rheumatoid arthritis. Confirmation by in vivo biochemical findings. , 1994, The Journal of rheumatology.

[147]  C. Wagner,et al.  Tissue distribution of glycine N-methyltransferase, a major folate-binding protein of liver. , 1994, Proceedings of the National Academy of Sciences of the United States of America.

[148]  P. Wilson,et al.  Vitamin status and intake as primary determinants of homocysteinemia in an elderly population. , 1993, JAMA.

[149]  K. Takahashi,et al.  Metabolic fate of cysteine sulfur in growing rats at various dietary protein levels. , 1993, Journal of nutritional science and vitaminology.

[150]  M. Kotb,et al.  Methionine adenosyltransferase: structure and function. , 1993, Pharmacology & therapeutics.

[151]  C. Wagner,et al.  Purification and properties of pancreatic glycine N-methyltransferase. , 1992, The Journal of biological chemistry.

[152]  M. Stipanuk,et al.  The splanchnic organs, liver and kidney have unique roles in the metabolism of sulfur amino acids and their metabolites in rats. , 1992, The Journal of nutrition.

[153]  M. Stipanuk,et al.  Cysteine concentration regulates cysteine metabolism to glutathione, sulfate and taurine in rat hepatocytes. , 1992, The Journal of nutrition.

[154]  J. Selhub,et al.  The pathogenesis of homocysteinemia: interruption of the coordinate regulation by S-adenosylmethionine of the remethylation and transsulfuration of homocysteine. , 1992, The American journal of clinical nutrition.

[155]  D. Weir,et al.  Betaine-homocysteine methyltransferase: organ distribution in man, pig and rat and subcellular distribution in the rat. , 1991, Clinical science.

[156]  K. Storch,et al.  Methionine kinetics in adult men: effects of dietary betaine on L-[2H3-methyl-1-13C]methionine. , 1991, The American journal of clinical nutrition.

[157]  K. Storch,et al.  Methionine kinetics and balance at the 1985 FAO/WHO/UNU intake requirement in adult men studied with L-[2H3-methyl-1-13C]methionine as a tracer. , 1991, The American journal of clinical nutrition.

[158]  C. Krieger,et al.  Amyotrophic lateral sclerosis , 1991, Neurology.

[159]  R. Akagi,et al.  Excretion of 3-mercaptolactate-cysteine mixed disulfide, sulfate and taurine in human urine before and after oral administration of sulfur-containing amino acids. , 1990, Acta medica Okayama.

[160]  M. Stipanuk,et al.  Catabolism of cyst(e)ine by rat renal cortical tubules. , 1990, The Journal of nutrition.

[161]  R. Waring,et al.  Plasma cysteine and sulphate levels in patients with motor neurone, Parkinson's and Alzheimer's disease , 1990, Neuroscience Letters.

[162]  M. Tappaz,et al.  Specific Antiserum and Monoclonal Antibodies Against the Taurine Biosynthesis Enzyme Cysteine Sulfinate Decarboxylase: Identity of Brain and Liver Enzyme , 1990, Journal of neurochemistry.

[163]  M. Stipanuk,et al.  Role of the transsulfuration pathway and of gamma-cystathionase activity in the formation of cysteine and sulfate from methionine in rat hepatocytes. , 1990, The Journal of nutrition.

[164]  M. Stipanuk,et al.  Metabolism of cyst(e)ine in rat enterocytes. , 1989, The Journal of nutrition.

[165]  J. Kopple,et al.  Plasma and urine taurine levels in vegans. , 1988, The American journal of clinical nutrition.

[166]  O. Griffith,et al.  Cysteinesulfonate and beta-sulfopyruvate metabolism. Partitioning between decarboxylation, transamination, and reduction pathways. , 1988, The Journal of biological chemistry.

[167]  K. Sugiyama,et al.  Effect of dietary glycine on methionine metabolism in rats fed a high-methionine diet. , 1987, Journal of nutritional science and vitaminology.

[168]  M. Stipanuk,et al.  Metabolism of cysteine in rat hepatocytes. Evidence for cysteinesulphinate-independent pathways. , 1987, The Biochemical journal.

[169]  J. Mitchell,et al.  Therapeutic doses of acetaminophen stimulate the turnover of cysteine and glutathione in man. , 1987, Journal of hepatology.

[170]  T. Sanders,et al.  Taurine concentrations in the diet, plasma, urine and breast milk of vegans compared with omnivores , 1986, British Journal of Nutrition.

[171]  S. Goss Characterization of cystathionine synthase as a selectable, liver-specific trait in rat hepatomas. , 1986, Journal of cell science.

[172]  P. Ueland,et al.  Determination of in vivo protein binding of homocysteine and its relation to free homocysteine in the liver and other tissues of the rat. , 1986, The Journal of biological chemistry.

[173]  T. Chase,et al.  New evidence for taurine biosynthesis in man obtained from 18O2 inhalation studies. , 1986, Life sciences.

[174]  J. Finkelstein,et al.  Methionine metabolism in mammals. Adaptation to methionine excess. , 1986, The Journal of biological chemistry.

[175]  A. Beenakkers,et al.  Influences of the ncc axons on electrical activity in the glandular lobe of the corpus cardiacum of Locusta migratoria , 1986 .

[176]  M. Stipanuk Metabolism of sulfur-containing amino acids. , 1986, Annual review of nutrition.

[177]  J. Crawhall A review of the clinical presentation and laboratory findings in two uncommon hereditary disorders of sulfur amino acid metabolism, beta-mercaptolactate cysteine disulfideuria and sulfite oxidase deficiency. , 1985, Clinical biochemistry.

[178]  P. Ueland,et al.  Radioenzymic determination of homocysteine in plasma and urine. , 1985, Clinical chemistry.

[179]  D. Carson,et al.  Differential regulation of polyamine synthesis and transmethylation reactions in methylthioadenosine phosphorylase deficient mammalian cells. , 1985, Biochimica et biophysica acta.

[180]  T. Eloranta,et al.  Catabolism and lability of S-adenosyl-L-methionine in rat liver extracts. , 1984, The Biochemical journal.

[181]  G. Boss,et al.  Decreased methionine synthesis in purine nucleoside-treated T and B lymphoblasts and reversal by homocysteine. , 1984, The Journal of clinical investigation.

[182]  J. Finkelstein,et al.  Methionine metabolism in mammals. Distribution of homocysteine between competing pathways. , 1984, The Journal of biological chemistry.

[183]  M. Stipanuk,et al.  Metabolism of cysteine, cysteinesulfinate and cysteinesulfonate in rats fed adequate and excess levels of sulfur-containing amino acids. , 1984, The Journal of nutrition.

[184]  C. Danzin,et al.  A rapid high-performance liquid chromatographic procedure for the simultaneous determination of methionine, ethionine, S-adenosylmethionine, S-adenosylethionine, and the natural polyamines in rat tissues. , 1984, Analytical biochemistry.

[185]  G. Hermansson,et al.  Sulfur amino acid metabolism in juvenile-onset nonketotic and ketotic diabetic patients. , 1984, Metabolism: clinical and experimental.

[186]  M. Galli-Kienle,et al.  Transmethylation, transsulfuration, and aminopropylation reactions of S-adenosyl-L-methionine in vivo. , 1984, The Journal of biological chemistry.

[187]  P. Trackman,et al.  Methionine synthesis from 5'-S-Methylthioadenosine. Resolution of enzyme activities and identification of 1-phospho-5-S methylthioribulose. , 1983, The Journal of biological chemistry.

[188]  D. Sullivan,et al.  Fractionation and kinetic properties of rat liver and kidney methionine adenosyltransferase isozymes. , 1983, Biochemistry.

[189]  J. Finkelstein,et al.  Regulation of hepatic betaine-homocysteine methyltransferase by dietary betaine. , 1983, The Journal of nutrition.

[190]  M. S. Wells,et al.  Human hepatic methionine biosynthesis. Purification and characterization of betaine:homocysteine S-methyltransferase. , 1982, The Journal of biological chemistry.

[191]  M. Stipanuk,et al.  The effect of dietary cysteine level on cysteine metabolism in rats. , 1982, The Journal of nutrition.

[192]  Fraunfelder Ft Transdermal scopolamine precipitating narrow-angle glaucoma. , 1982 .

[193]  J. J. Martin,et al.  Regulation of hepatic betaine-homocysteine methyltransferase by dietary methionine. , 1982, Biochemical and biophysical research communications.

[194]  M. Stipanuk,et al.  Characterization of the enzymic capacity for cysteine desulphhydration in liver and kidney of the rat. , 1982, The Biochemical journal.

[195]  J. Foreman,et al.  Homocystine uptake in isolated rat renal cortical tubules. , 1982, Metabolism: clinical and experimental.

[196]  J. Mårtensson The effects of short-term fasting on the excretion of sulfur compounds in healthy subjects. , 1982, Metabolism: clinical and experimental.

[197]  C. Herring,et al.  Adenosine metabolism: modification by S-adenosylhomocysteine and 5'-methylthioadenosine. , 1982, Archives of biochemistry and biophysics.

[198]  S. Zlotkin,et al.  The Development of Cystathionase Activity During the First Year of Life , 1982, Pediatric Research.

[199]  W. Oertel,et al.  Comparison of cysteine sulphinic acid decar☐ylase isoenzymes and glutamic acid decar☐ylase in rat liver and brain , 1981, Neuroscience.

[200]  R. Billings,et al.  The role of methionine in regulating folate-dependent reactions in isolated rat hepatocytes. , 1981, Archives of biochemistry and biophysics.

[201]  W. Schütz,et al.  Role of S-adenosylhomocysteine hydrolase in adenosine metabolism in mammalian heart. , 1981, The Biochemical journal.

[202]  R. Smith,et al.  Methionine synthesis from 5'-methylthioadenosine in rat liver. , 1981, The Journal of biological chemistry.

[203]  D. Marion,et al.  S-Adenosylmethionine and S-adenosylhomocystein metabolism in isolated rat liver. Effects of L-methionine, L-homocystein, and adenosine. , 1980, The Journal of biological chemistry.

[204]  P. Mandel,et al.  Cysteine sulfinate aminotransferase and aspartate aminotransferase isoenzymes of rat brain. Purification, characterization, and further evidence for identity. , 1980, Biochemistry.

[205]  C. Scriver,et al.  Labile methyl group balances in the human: the role of sarcosine. , 1980, Metabolism: clinical and experimental.

[206]  P. Chiang,et al.  The Role of S-Adenosylhomocysteine and S-Adenosylhomocysteine Hydrolase in the Control of Biological Methylations , 1980 .

[207]  M. Stipanuk Effect of excess dietary methionine on the catabolism of cysteine in rats. , 1979, The Journal of nutrition.

[208]  H. Kagamiyama,et al.  Cysteine sulfinate transamination activity of aspartate aminotransferases. , 1979, Biochemical and biophysical research communications.

[209]  D. Hoffman,et al.  Relationship between tissue levels of S-adenosylmethionine, S-adenylhomocysteine, and transmethylation reactions. , 1979, Canadian journal of biochemistry.

[210]  W. B. Quay,et al.  Cystathionine synthase in rat brain: Regional and time‐of‐day differences and their metabolic implications , 1979, Journal of neuroscience research.

[211]  K. Yamaguchi,et al.  Dietary control of cysteine dioxygenase in rat liver. , 1978, Journal of biochemistry.

[212]  Y. Kori,et al.  Rat liver cysteine dioxygenase (cysteine oxidase). Further purification, characterization, and analysis of the activation and inactivation. , 1978, Journal of biochemistry.

[213]  T. Eloranta Tissue distribution of S-adenosylmethionine and S-adenosylhomocysteine in the rat. Effect of age, sex and methionine administration on the metabolism of S-adenosylmethionine, S-adenosylhomocysteine and polyamines. , 1977, The Biochemical journal.

[214]  M. Stipanuk,et al.  Effect of cystine on the metabolism on methionine in rats. , 1977, The Journal of nutrition.

[215]  D. Rassin,et al.  Milk protein quantity and quality in low-birth-weight infants: II. Effects on selected aliphatic amino acids in plasma and urine. , 1977, Pediatrics.

[216]  T. Eloranta,et al.  A new method for the assay of tissue. S-adenosylhomocysteine and S-adenosylmethione. Effect of pyridoxine deficiency on the metabolism of S-adenosylhomocysteine, S-adenosylmethionine and polyamines in rat liver. , 1976, The Biochemical journal.

[217]  S. Mudd,et al.  Labile methyl balances for normal humans on various dietary regimens. , 1975, Metabolism: clinical and experimental.

[218]  W. A. Edwards,et al.  Homocystinuria due to cystathionine synthase deficiency. Studies of nitrogen balance and sulfur excretion. , 1975, The Journal of clinical investigation.

[219]  F. Chatagner,et al.  Rat liver cysteine sulfinate decarboxylase: purification, new appraisal of the molecular weight and determination of catalytic properties. , 1975, Biochimica et biophysica acta.

[220]  J. Finkelstein,et al.  Methionine metabolism in mammals: regulatory effects of S-adenosylhomocysteine. , 1974, Archives of biochemistry and biophysics.

[221]  J. Finkelstein,et al.  Methionine metabolism in mammals: kinetic study of betaine-homocysteine methyltransferase. , 1972, Archives of biochemistry and biophysics.

[222]  S. Kerr Competing methyltransferase systems. , 1972, The Journal of biological chemistry.

[223]  J. Sturman,et al.  Development of Mammalian Sulfur Metabolism: Absence of Cystathionase in Human Fetal Tissues , 1972, Pediatric Research.

[224]  E. Stokstad,et al.  Mammalian methylenetetrahydrofolate reductase. Partial purification, properties, and inhibition by S-adenosylmethionine. , 1971, Biochimica et biophysica acta.

[225]  J. Finkelstein,et al.  Methionine metabolism in mammals: Effects of age, diet, and hormones on three enzymes of the pathway in rat tissues , 1967 .

[226]  A. Koj,et al.  [35S]thiosulphate oxidation by rat liver mitochondria in the presence of glutathione. , 1967, The Biochemical journal.

[227]  J. Finkelstein,et al.  Transsulfuration in mammals. Microassays and tissue distributions of three enzymes of the pathway. , 1965, The Journal of biological chemistry.

[228]  B. Skarżyński,et al.  The Metabolic State of Thiosulphate , 1961, Nature.