Vitamin b 1 (thiamine). a cofactor for enzymes involved in the main metabolic pathways and an environmental stress protectant

Advances in Botanical Research

Volumn 58, Issue , 2011, Pages 37-91

  Rapala Kozik, Maria ^a  

^a JAGIELLONIAN UNIVERSITY   (Poland)

Author keywords

Antioxidants; Biotic and abiotic stress; Thiamine biosynthesis; Thiamine diphosphate dependent enzymes

Indexed keywords

EID: 80051558945     PISSN: 00652296     EISSN: None     Source Type: Book Series    
DOI: 10.1016/B978-0-12-386479-6.00004-4     Document Type: Chapter

References (265)

1. Adamek-Swierczynska S., Kozik A. Multiple thiamine-binding proteins of legume seeds. Thiamine-binding vicilin of Vicia faba versus thiamine-binding albumin of Pisum sativum. Plant Physiology and Biochemistry 2002, 40:735-741.
2. Adamek-Swierczynska S., Rapala-Kozik M., Kozik A. Purification and preliminary characterisation of a thiamine-binding protein from maize seeds. Journal of Plant Physiology 2000, 156:635-639.
3. Agyei-Owusu K., Leeper F.J. Thiamin diphosphate in biological chemistry: Analogues of thiamin diphosphate in studies of enzymes and riboswitches. The FEBS Journal 2009, 276:2905-2916.
4. Ahn I.P., Kim S., Lee Y.H. Vitamin B1 functions as an activator of plant disease resistance. Plant Physiology 2005, 138:1505-1515.
5. Ahn I.P., Kim S., Lee Y.H., Suh S.C. Vitamin B1-induced priming is dependent on hydrogen peroxide and the NPR1 gene in Arabidopsis. Plant Physiology 2007, 143:838-848.
6. Ajjawi I., Rodriguez Milla M.A., Cushman J., Shintani D.K. Thiamin pyrophosphokinase is required for thiamin cofactor activation in Arabidopsis. Plant Molecular Biology 2007, 65:151-162.
7. Ajjawi I., Tsegaye Y., Shintani D. Determination of the genetic, molecular, and biochemical basis of the Arabidopsis thaliana thiamin auxotroph th1. Archives of Biochemistry and Biophysics 2007, 459:107-114.
8. Anderson M.D., Che P., Song J., Nikolau B.J., Wurtele E.S. 3-Methylcrotonyl-coenzyme A carboxylase is a component of the mitochondrial leucine catabolic pathway in plants. Plant Physiology 1998, 118:1127-1138.
9. Araújo W.L., Nunes-Nesi A., Trenkamp S., Bunik V.I., Fernie A.R. Inhibition of 2-oxoglutarate dehydrogenase in potato tuber suggests the enzyme is limiting for respiration and confirms its importance in nitrogen assimilation. Plant Physiology 2008, 148:1782-1796.
10. Arora A., Sairam R.K., Srivastava G.C. Oxidative stress and antioxidative system in plants. Current Science 2002, 82:1227-1238.
11. Baker L.J., Dorocke J.A., Harris R.A., Timm D.E. The crystal structure of yeast thiamin pyrophosphokinase. Structure 2001, 9:539-546.
12. Balakumar P., Rohilla A., Krishan P., Solairaj P., Thangathirupathi A. The multifaceted therapeutic potential of benfotiamine. Pharmacological Research 2010, 61:482-488.
13. Balmer Y., Koller A., del Val G., Manieri W., Schurmann P., Buchanan B.B. Proteomics gives insight into the regulatory function of chloroplast thioredoxins. Proceedings of the National Academy of Sciences of the United States of America 2003, 100:370-375.
14. Barile M., Passarella S., Quagliariello E. Thiamine pyrophosphate uptake into isolated rat liver mitochondria. Archives of Biochemistry and Biophysics 1990, 280:352-357.
15. Baxter C.J., Redestig H., Schauer N., Repsilber D., Patil K.R., Nielsen J., Selbig J., Liu J., Fernie A.R., Sweetlove L.J. The metabolic response of heterotrophic Arabidopsis cells to oxidative stress. Plant Physiology 2007, 143:312-325.
16. Begley T.P., Downs D.M., Ealick S.E., Mc Lafferty F.W., Van Loon A.P., Taylor S., Campobasso N., Chiu H.J., Kinsland C., Reddick J.J., Xi J. Thiamin biosynthesis in prokaryotes. Archives of Microbiology 1999, 171:293-300.
17. Begley T.P., Chatterjee A., Hanes J.W., Hazra A., Ealick S.E. Cofactor biosynthesis-Still yielding fascinating new biological chemistry. Current Opinion in Chemical Biology 2008, 12:118-125.
18. Belanger F., Leustek T., Chu B., Kirz A. Evidence for the thiamine biosynthetic pathway in higher plant plastids and its developmental regulation. Plant Molecular Biology 1995, 29:809-821.
19. Bernacchia G., Schwall G., Lottspeich F., Salamini F., Bartels D. The transketolase gene family of the resurrection plant Craterostigma plantagineum: Differential expression during the rehydration phase. The EMBO Journal 1995, 14:610-618.
20. Bernasconi P., Woodworth A.R., Rosen B.A., Subramanian M.V., Siehl D.L. A naturally occurring point mutation confers broad range tolerance toherbicides that target acetolactate synthase. The Journal of Biological Chemistry 1995, 270:17381-17385.
21. Bettendorff L. Thiamine homeostasis in neuroblastoma cells. Neurochemistry International 1995, 26:295-302.
22. Bettendorff L., Wins P. Thiamin diphosphate in biological chemistry: New aspects of thiamin metabolism, especially triphosphate derivatives acting other than as cofactors. The FEBS Journal 2009, 276:2917-2925.
23. Bettendorff L., Kolb H.A., Schoffeniels E. Thiamine triphosphate activates an anion channel of large unit conductance in neuroblastoma cells. The Journal of Membrane Biology 1993, 136:281-288.
24. Bettendorff L., Wirtzfeld B., Makarchikov A.F., Mazzucchelli G., Frédérich M., Gigliobianco T., Gangolf M., De Pauw E., Angenot L., Wins P. Discovery of a natural thiamine adenine nucleotide. Nature Chemical Biology 2007, 3:211-212.
25. Bocobza S., Aharoni A. Switching the light on plant riboswitches. Trends in Plant Science 2008, 13:526-533.
26. Bocobza S., Adato A., Mandel T., Shapira M., Nudler E., Aharoni A. Riboswitch-dependent gene regulation and its evolution in the plant kingdom. Genes & Development 2007, 21:2874-2879.
27. Bos M., Kozik A. Some molecular and enzymatic properties of a homogeneous preparation of thiaminase I purified from carp liver. Journal of Protein Chemistry 2000, 19:75-84.
28. Breaker R.R. Riboswitches and the RNA World. Cold Spring Harbor Perspectives in Biology 2010, 10.1101/cshperspect.a003566.
29. Bunik V.I., Fernie A.R. Metabolic control exerted by the 2-oxoglutarate dehydrogenase reaction: A cross-kingdom comparison of the crossroad between energy production and nitrogen assimilation. The Biochemical Journal 2009, 422:405-421.
30. Camp P.J., Randall D.D. Purification and characterization of the pea chloroplast pyruvate dehydrogenase complex: A source of acetyl-CoA and NADH for fatty acid biosynthesis. Plant Physiology 1985, 77:571-577.
31. Chabregas S.M., Luche D.D., Farias L.P., Ribeiro A.F., van Sluys M.A., Menck C.F., Silva-Filho M.C. Dual targeting properties of the N-terminal signal sequence of Arabidopsis thaliana THI1 protein to mitochondria and chloroplasts. Plant Molecular Biology 2001, 46:639-650.
32. Chabregas S.M., Luche D.D., Van Sluys M.A., Menck C.F., Silva-Filho M.C. Differential usage of two in-frame translational start codons regulates subcellular localization of Arabidopsis thaliana THI1. Journal of Cell Science 2003, 116:285-291.
33. Chang A.K., Duggleby R.G. Expression, purification and characterization of Arabidopsis thaliana acetohydroxyacid synthase. The Biochemical Journal 1997, 327:161-169.
34. Chang A.K., Duggleby R.G. Herbicide resistant forms of Arabidopsis thaliana acetohydroxyacid synthase: Characterization of the catalytic properties and sensitivity to inhibitors of four defined mutants. The Biochemical Journal 1998, 333:765-777.
35. Chang S.I., Kang M.K., Choi J.D., Namgoong S.K. Soluble overexpression in Escherichia coli, and purification and characterization of wild-type recombinant tobacco acetolactate synthase. Biochemical and Biophysical Research Communications 1997, 234:549-553.
36. Chatterjee A., Jurgenson C.T., Schroeder F.C., Ealick S.E., Begley T.P. Thiamin biosynthesis in eukaryotes: Characterization of the enzyme-bound product of thiazole synthase from Saccharomyces cerevisiae and its implications in thiazole biosynthesis. Journal of the American Chemical Society 2006, 128:7158-7159.
37. Chatterjee A., Jurgenson C.T., Schroeder F.C., Ealick S.E., Begley T.P. Biosynthesis of thiamin thiazole in eukaryotes: Conversion of NAD to an advanced intermediate. Journal of the American Chemical Society 2007, 129:2914-2922.
38. Chatterjee A., Li Y., Zhang Y., Grove T.L., Lee M., Krebs C., Booker S.J., Begley T.P., Ealick S.E. Reconstitution of ThiC in thiamine pyrimidine biosynthesis. Nature Chemical Biology 2008, 4:758-765.
39. Chatterjee A., Schroeder F.C., Jurgenson C.T., Ealick S.E., Begley T.P. Biosynthesis of the thiamin-thiazole in eukaryotes: Identification of a thiazole tautomer intermediate. Journal of the American Chemical Society 2008, 130:11394-11398.
40. Cheah M.T., Wachter A., Sudarsan N., Breaker R.R. Control of alternative RNA splicing and gene expression by eukaryotic riboswitches. Nature 2007, 447:497-500.
41. Cheng G., Bennett E.M., Begley T.P., Ealick S.E. Crystal structure of 4-amino-5-hydroxymethyl-2-methylpyrimidine phosphate kinase from Salmonella typhimurium at 2.3 A resolution. Structure 2002, 10:225-235.
42. Chiu H.J., Reddick J.J., Begley T.P., Ealick S.E. Crystal structure of thiamin phosphate synthase from Bacillus subtilis at 1.25 A resolution. Biochemistry 1999, 38:6460-6470.
43. Conley T.R., Peng H.P., Shih M.C. Mutations affecting induction of glycolytic and fermentative genes during germination and environmental stress in Arabidopsis. Plant Physiology 1999, 119:599-607.
44. Cordoba E., Salmi M., León P. Unravelling the regulatory mechanisms that modulate the MEP pathway in higher plants. Journal of Experimental Botany 2009, 60:2933-2943.
45. Couée I., Sulmon C., Gouesbet G., El Amrani A. Involvement of soluble sugars in reactive oxygen species balance and responses to oxidative stress in plants. Journal of Experimental Botany 2006, 57:449-459.
46. Debnam P.M., Emes M.J. Subcellular distribution of enzymes of the oxidative pentose phosphate pathway in root and leaf tissues. Journal of Experimental Botany 1999, 50:1653-1661.
47. Debnam P.M., Fernie A.R., Leisse A., Golding A., Bowsher C.G., Grimshaw C., Knight J.S., Emes M.J. Altered activity of the P2 isoform of plastidic glucose 6-phosphate dehydrogenase in tobacco (Nicotiana tabacum cv. Samsun) causes changes in carbohydrate metabolism and response to oxidative stress in leaves. The Plant Journal 2004, 38:49-59.
48. Dorrestein P.C., Zhai H., McLafferty F.W., Begley T.P. The biosynthesis of the thiazole phosphate moiety of thiamin: The sulfur transfer mediated by the sulfur carrier protein ThiS. Chemistry & Biology 2004, 11:1373-1381.
49. Douce R., Neuburger M. The uniqueness of plant mitochondria. Annual Review of Plant Physiology and Plant Molecular Biology 1989, 40:371-414.
50. Drew M.C. Oxygen deficiency and root metabolism: Injury and acclimation under hypoxia and anoxia. Annual Review of Plant Physiology and Plant Molecular Biology 1997, 48:223-250.
51. Duggleby R.G. Domain relationships in thiamine diphosphate-dependent enzymes. Accounts of Chemical Research 2006, 39:550-557.
52. Duggleby R.G., McCourt J.A., Guddat L.W. Structure and mechanism of inhibition of plant acetohydroxyacid synthase. Plant Physiology and Biochemistry 2008, 46:309-324.
53. Dumas R., Biou V., Douce R. Purification and characterization of a fusion protein of plant acetohydroxy acid synthase and acetohydroxy acid isomeroreductase. FEBS Letter 1997, 408:156-160.
54. Durner J., Boger P. Acetolactate synthase from barley (Hordeum vulgare L.): Purification and partial characterization. Zeitschrift für Naturforschung 1988, 43C:850-856.
55. Estevez J.M., Cantero A., Reindl A., Reichler S., Leon P. 1-Deoxy-D-xylulose-5-phosphate synthase, a limiting enzyme for plastidic isoprenoid biosynthesis in plants. The Journal of Biological Chemistry 2001, 276:22901-22909.
56. Faith C.B., Thomas L., Boyang C., Alan L.K. Evidence for the thiamine biosynthetic pathway in higher-plant plastids and its developmental regulation. Plant Molecular Biology 1995, 29:809-821.
57. 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. Annals of Botany 2006, 98:361-377.
58. Flechner A., Dressen U., Westhoff P., Henze K., Schnarrenberger C., Martin W. Molecular characterization of transketolase (EC 2.2.1.1) active in the Calvin cycle of spinach chloroplasts. Plant Molecular Biology 1996, 32:475-484.
59. Fleming J.C., Tartaglini E., Steinkami M.P., Schorderet D.F., Cohen N., Neufeldt E.J. The gene mutated in thiamine-responsive anaemia with diabetes and deafness (TRMA) encodes a functional thiamine transporter. Nature Genetics 1999, 22:305-308.
60. Forlani G., Mantelli M., Nielsen E. Biochemical evidence for multiple acetoin-forming enzymes in cultured plant cells. Phytochemistry 1999, 50:255-262.
61. Frank R.A., Leeper F.J., Luisi B.F. Structure, mechanism and catalytic duality of thiamine-dependent enzymes. Cellular and Molecular Life Science 2007, 64:892-905.
62. Frédérich M., Delvaux D., Gigliobianco T., Gangolf M., Dive G., Mazzucchelli G., Elias B., De Pauw E., Angenot L., Wins P., Bettendorff L. Thiaminylated adenine nucleotides. Chemical synthesis, structural characterization and natural occurrence. The FEBS Journal 2009, 276:3256-3268.
63. Fujiki Y., Sato T., Ito M., Watanabe A. Isolation and characterization of cDNA clones for the e1beta and E2 subunits of the branched-chain alpha-ketoacid dehydrogenase complex in Arabidopsis. The Journal of Biological Chemistry 2000, 275:6007-6013.
64. Fujiwara M. Allithiamine and itsproperties. Journal of Nutritional Science and Vitaminology (Tokyo) 1976, 22:57-62.
65. Funk C. The etiology of the deficiency diseases. Beri-beri, polyneuritis in birds, epidemic dropsy, scurvy, experimental scurvy in animals, infantile scurvy, ship beri-beri, pellagra. Journal of State Medicine 1912, 20:341-368.
66. Gangolf M., Czerniecki J., Radermecker M., Detry O., Nisolle M., Jouan C., Martin D., Chantraine F., Lakaye B., Wins P., Grisar T., Bettendorff L. Thiamine status in humans and content of phosphorylated thiamine derivatives in biopsies and cultured cells. PloS ONE 2010, 5:13616-13629.
67. Gangolf M., Wins P., Thiry M., El Moualij B., Bettendorff L. Thiamine triphosphate synthesis in rat brain occurs in mitochondria and is coupled to the respiratory chain. The Journal of Biological Chemistry 2010, 285:583-594.
68. Gass N., Glagotskaia T., Mellema S., Stuurman J., Barone M., Mandel T., Roessner-Tunali U., Kuhlemeier C. Pyruvate decarboxylase provides growing pollen tubes with a competitive advantage in petunia. The Plant Cell 2005, 17:2355-2368.
69. Geddes W.F., Levine M.N. The distribution of thiamin in the wheat plant at successive stage of kernel development. Cereal Chemistry 1942, 19:547-552.
70. Gibson G.E., Blass J.P. Thiamine-dependent processes and treatment strategies in neurodegeneration. Antioxidants & Redox Signaling 2007, 9:1605-1619.
71. Gibson G.E., Zhang H. Interactions of oxidative stress with thiamine homeostasis promote neurodegeneration. Neurochemistry International 2002, 40:493-504.
72. Gigliobianco T., Lakaye B., Wins P., El Moualij B., Zorzi W., Bettendorff L. Adenosine thiamine triphosphate accumulates in Escherichia coli cells in response to specific conditions of metabolic stress. BMC Microbiology 2010, 10:148-152.
73. Godoi P.H., Galhardo R.S., Luche D.D., Van Sluys M.A., Menck C.F., Oliva G. Structure of the thiazole biosynthetic enzyme THI1 from Arabidopsis thaliana. The Journal of Biological Chemistry 2006, 281:30957-30966.
74. Golda A., Szyniarowski P., Ostrowska K., Kozik A., Rapala-Kozik M. Thiamine binding and metabolism in germinating seeds of selected cereals and legumes. Plant Physiology and Biochemistry 2004, 42:187-195.
75. Goyer A. Thiamine in plants: Aspects of its metabolism and functions. Phytochemistry 2010, 71:1615-1624.
76. Hakim A.M. The induction and reversibility of cerebral acidosis in thiamine deficiency. Annals of Neurology 1984, 16:673-679.
77. Hanes J.W., Ealick S.E., Begley T.P. Thiamin phosphate synthase: The rate of pyrimidine carbocation formation. Journal of the American Chemical Society 2007, 129:4860-4861.
78. Hazell A.S. Astrocytes are a major target in thiamine deficiency and Wernicke's encephalopathy. Neurochemistry International 2009, 55:129-135.
79. Hazell A.S., Butterworth R.F. Update of cell damage mechanisms in thiamine deficiency: Focus on oxidative stress, excitotoxicity and inflammation. Alcohol and Alcoholism 2009, 44:141-147.
80. Hazell A.S., Todd K.G., Butterworth R.F. Mechanisms of neuronal cell death in Wernicke's encephalopathy. Metabolic Brain Disease 1998, 13:97-122.
81. Henkes S., Sonnewald U., Badur R., Flachmann R., Stitt M. A small decrease of plastid transketolase activity in antisense tobacco transformants has dramatic effects on photosynthesis and phenylpropanoid metabolism. The Plant Cell 2001, 13:535-551.
82. Héroux M., Butterworth R.F. Regional alterations of thiamine phosphate esters and of thiamine diphosphate-dependent enzymes in relation to function in experimental Wernicke's encephalopathy. Neurochemical Research 1995, 20:87-93.
83. Hilker D.M., Somogyi J.C. Antithiamins of plant origin: Their chemical nature and mode of action. Annals of the New York Academy of Sciences 1982, 378:137-145.
84. Hill R.E., Himmeldirk K., Kennedy I.A., Pauloski R.M., Sayer B.G., Wolf E., Spenser I.D. The biogenetic anatomy of vitamin B6. A 13C NMR investigation of the biosynthesis of pyridoxol in Escherichia coli. The Journal of Biological Chemistry 1996, 271:30426-30435.
85. Hix L.M., Lockwood S.F., Bertram J.S. Bioactive carotenoids: Potent antioxidants and regulators of gene expression. Redox Report 2004, 9:181-191.
86. Hohmann S., Meacock P.A. Thiamin metabolism and thiamin diphosphate-dependent enzymes in the yeast Saccharomyces cerevisiae: Genetic regulation. Biochimica et Biophysica Acta 1998, 1385:201-219.
87. Hong Z.Q., Copeland L. Pentose phosphate pathway enzymes in nitrogen-fxing leguminous root nodules. Phytochemistry 1990, 29:2437-2440.
88. Hossain M.A., Hug E., Hodges T.K. Sequence of a cDNA from Oryza sativa (L.) encoding the pyruvate decarboxylase 1 gene. Plant Physiology 1994, 106:799-800.
89. Huang H.M., Chen H.L., Gibson G.E. Thiamine and oxidants interact to modify cellular calcium stores. Neurochemical Research 2010, 35:2107-2116.
90. Iacopetta D., Carrisi C., De Filippis G., Calcagnile V.M., Cappello A.R., Chimento A., Curcio R., Santoro A., Vozza A., Dolce V., Palmieri F., Capobianco L. The biochemical properties of the mitochondrial thiamine pyrophosphate carrier from Drosophila melanogaster. The FEBS Journal 2010, 277:1172-1181.
91. Ismail A.M., Ella E.S., Vergara G.V., Mackill D.J. Mechanisms associated with tolerance for flooding during germination and early seedling growth in rice (Oryza sativa). Annals of Botany 2009, 103:197-209.
92. Ismond K.P., Dolferus R., de Pauw M., Dennis E.S., Good A.G. Enhanced low oxygen survival in Arabidopsis through increased metabolic flux in the fermentative pathway. Plant Physiology 2003, 132:1292-1302.
93. Jacob-Wilk D., Goldschmidt E.E., Riov J., Sadka A., Holland D. Induction of a Citrus gene highly homologous to plant and yeast thi genes involved in thiamine biosynthesis during natural and ethylene-induced fruit maturation. Plant Molecular Biology 1997, 35:661-666.
94. Jenkins A.H., Schyns G., Potot S., Sun G., Begley T.P. A new thiamin salvage pathway. Nature Chemical Biology 2007, 3:492-497.
95. Jordan F. Adenosine triphosphate and thiamine cross paths. Nature Chemical Biology 2007, 3:202-203.
96. Jordan F., Nemeria N.S., Zhang S., Yan Y., Arjunan P., Furey W. Dual catalytic apparatus of the thiamin diphosphate coenzyme: Acid-base via the 1',4'-iminopyrimidine tautomer along with its electrophilic role. Journal of the American Chemical Society 2003, 125:12732-12738.
97. Journet E.P., Douce R. Enzymic capacities of purified cauliflower bud plastids for lipid synthesis and carbohydrate metabolism. Plant Physiology 1985, 79:458-467.
98. Julliard J.H., Douce R. Biosynthesis of the thiazole moiety of thiamin (vitamin B1) in higher plant chloroplasts. Proceedings of the National Academy of Sciences of the United States of America 1991, 88:2042-2045.
99. Jung S.M., Le D.T., Yoon S.S., Yoon M.Y., Kim Y.T., Choi J.D. Amino acid residues conferring herbicide resistance in tobacco acetohydroxy acid synthase. The Biochemical Journal 2004, 383:53-61.
100. Jurgenson C.T., Begley T.P., Ealick S.E. The structural and biochemical foundations of thiamin biosynthesis. Annual Review of Biochemistry 2009, 78:569-603.
101. Kato-Noguchi H., Yasuda Y. Effect of low temperature on ethanolic fermentation in rice seedlings. Journal of Plant Physiology 2007, 164:1013-1018.
102. Kawai K., Kaku K., Izawa N., Shimizu T., Fukuda A., Tanaka Y. A novel mutant acetolactate synthase gene from rice cells, which confers resistance to ALS-inhibiting herbicides. Journal of Pesticide Science 2007, 32:89-98.
103. Kawasaki Y. Copurification of hydroxyethylthiazole kinase and thiamine-phosphate pyrophosphorylase of Saccharomyces cerevisiae: Characterization of hydroxyethylthiazole kinase as a bifunctional enzyme in the thiamine biosynthetic pathway. Journal of Bacteriology 1993, 175:5153-5158.
104. Kawasaki Y., Onozuka M., Mizote T., Nosaka K. Biosynthesis of hydroxymethylpyrimidine pyrophosphate in Saccharomyces cerevisiae. Current Genetics 2005, 47:156-162.
105. Ke J., Behal R.H., Back S.L., Nikolau B.J., Wurtele E.S., Oliver D.J. The role of pyruvate dehydrogenase and acetyl-coenzyme A synthetase in fatty acid synthesis in developing Arabidopsis seeds. Plant Physiology 2000, 123:497-508.
106. Kim Y.S., Nosaka K., Downs D.M., Kwak J.M., Park D., Chung I.K., Nam H.G. A Brassica cDNA clone encoding a bifunctional hydroxymethylpyrimidine kinase/thiamin-phosphate pyrophosphorylase involved in thiamin biosynthesis. Plant Molecular Biology 1998, 37:955-966.
107. Kim B.R., Kim S.U., Chang Y.J. Differential expression of three 1-deoxy-D-xylulose-5-phosphate synthase genes in rice. Biotechnology Letters 2005, 27:997-1001.
108. Kochibe N., Yusa T., Hyashi K. Occurrence of thiamine triphosphate in higher plants. Plant & Cell Physiology 1963, 4:239-244.
109. Kolkman J.M., Slabaugh M.B., Bruniard J.M., Berry S., Bushman B.S., Olungu C., Maes N., Abratti G., Zambelli A., Miller J.F., Leon A., Knapp S.J. Acetohydroxyacid synthase mutations conferring resistance to imidazolinone or sulfonylurea herbicides in sunflower. Theoretical and Applied Genetics 2004, 109:1147-1159.
110. Kondo K., Mitsuda H., Iwai K. Thiamine synthesis in leaves of cereal crops. Journal of Agricultural Chemical Society of Japan 1951, 24:128-132.
111. Kong D., Zhu Y., Wu H., Cheng X., Liang H., Ling H.Q. AtTHIC, a gene involved in thiamine biosynthesis in Arabidopsis thaliana. Cell Research 2008, 18:566-576.
112. Koornneef M., Hanhart C. A new thiamine locus in Arabidopsis. Arabidopsis Information Service 1981, 18:52-58.
113. Kowalska E., Kozik A. The genes and enzymes involved in the biosynthesis of thiamin and thiamin diphosphate in yeasts. Cellular & Molecular Biology Letters 2008, 13:271-282.
114. Kozik A., Rapala-Kozik M. Protein-attributable thiamine-binding activity in gymnosperm seeds. Journal of Plant Physiology 1995, 146:760-762.
115. Kozik A., Rapala-Kozik M. Comparative study on binding of thiamine-related compounds by extracts of seeds of Zea mays, Spinacia oleracea, Picea abies and Cycas revolute. Plant Physiology and Biochemistry 1996, 34:779-786.
116. Kriek M., Martins F., Leonardi R., Fairhurst S.A., Lowe D.J., Roach P.L. Thiazole synthase from Escherichia coli: An investigation of the substrates and purified proteins required for activity in vitro. The Journal of Biological Chemistry 2007, 282:17413-17423.
117. Krook J., Vreugdenhil D., Dijkema C., van der Plas L.H.W. Sucrose and starch metabolism in carrot (Daucuscarota L.) cell suspensions analysed by C-labelling: Indications for a cytosol and a plastid-localized oxidative pentose phosphate pathway. Journal of Experimental Botany 1998, 49:1917-1924.
118. Kruger N.J., von Schaewen A. The oxidative pentose phosphate pathway: Structure and organisation. Current Opinion in Plant Biology 2003, 6:236-246.
119. Kruszewski S.P., Jakobs W.P. Polarity of thiamine movement through tomato petioles. Plant Physiology 1974, 54:310-311.
120. Kürsteiner O., Dupuis I., Kuhlemeier C. The pyruvate decaroboxylase1 gene of Arabidopsis is required during anoxia but not other environmental stresses. Plant Physiology 2003, 132:968-978.
121. Kylen A., McCready R.M. Nutrients in seeds and sprouts of alfalfa, lentils, mung beans, and soybeans. Journal of Food Science 1975, 40:1008-1009.
122. Lakaye B., Wirtzfeld B., Wins P., Grisar T., Bettendorff L. Thiamine triphosphate, a new signal required for optimal growth of Escherichia coli during amino acid starvation. The Journal of Biological Chemistry 2004, 279:17142-17147.
123. Lange B.M., Wildung M.R., McCaskill D., Croteau R. A family of transketolases that directs isoprenoid biosynthesis via a mevalonate-independent pathway. Proceedings of the National Academy of Sciences of the United States of America 1998, 95:2100-2104.
124. Lee Y.T., Duggleby R.G. Identification of the regulatory subunit of Arabidopsis thaliana acetohydroxyacid synthase and reconstitution with its catalytic subunit. Biochemistry 2001, 40:6836-6844.
125. Lehmann M., Schwarzländer M., Obata T., Sirikantaramas S., Burow M., Olsen C.E., Tohge T., Fricker M.D., Møller B.L., Fernie A.R., Sweetlove L.J., Laxa M. The metabolic response of Arabidopsis roots to oxidative stress is distinct from that of heterotrophic cells in culture and highlights a complex relationship between the levels of transcripts, metabolites, and flux. Molecular Plant 2009, 2:390-406.
126. Lemaire S.D., Guillon B., Le Marechal P., Keryer E., Miginiac-Maslow M., Decottignies P. New thioredoxin targets in the unicellular photosynthetic eukaryote Chlamydomonas reinhardtii. Proceedings of the National Academy of Sciences of the United States of America 2004, 101:7475-7480.
127. Lichtenthaler H.K. The 1-deoxy-D-phosphate pathway of isoprenoid biosynthesis in plants. Annual Review of Plant Physiology and Plant Molecular Biology 1999, 50:47-65.
128. Lichtenthaler H.K., Schwender J., Disch A., Rohmer M. Biosynthesis of isoprenoids in higher plant chloroplasts proceeds via a mevalonate-independent pathway. FEBS Letters 1997, 400:271-274.
129. Lindhurst M.J., Fiermonte G., Song S., Struys E., De Leonardis F., Schwartzberg P.L., Chen A., Castegna A., Verhoeven N., Mathews C.K., Palmieri F., Biesecker L.G. Knockout of Slc25a19 causes mitochondrial thiamine pyrophosphate depletion, embryonic lethality, CNS malformations, and anemia. Proceedings of the National Academy of Sciences of the United States of America 2006, 103:15927-15932.
130. Lindqvist Y., Schneider G., Ermler U., Sundström M. Three-dimensional structure of transketolase, a thiamine diphosphate dependent enzyme, at 2.5 A resolution. The EMBO Journal 1992, 11:2373-2379.
131. Lois L.M., Rodriguez-Concepcion M., Gallego F., Campos N., Boronat A. Carotenoid biosynthesis during tomato fruit development: Regulatory role of 1-deoxy-D-xylulose5-phosphate synthase. The Plant Journal 2000, 22:503-513.
132. Lonsdale D. A review of the biochemistry, metabolism and clinical benefits of thiamin(e) and its derivatives. Evidence Based Complementary and Alternative Medicine 2006, 3:49-59.
133. Luethy M.H., Gemel J., Johnston M.L., Mooney B.P., Miernyk J.A., Randall D.D. Developmental expression of the mitochondrial pyruvate dehydrogenase complex in pea (Pisum sativum) seedlings. Physiologia Plantarum 2001, 112:559-566.
134. Lukienko P.I., Mel'nichenko N.G., Zverinskii I.V., Zabrodskaya S.V. Antioxidant properties of thiamine. Bulletin of Experimental Biology and Medicine 2000, 130:874-876.
135. Machado C.R., de Oliveira R.L., Boiteux S., Praekelt U.M., Meacock P.A., Menck C.F. Thi1, a thiamine biosynthetic gene in Arabidopsis thaliana, complements bacterial defects in DNA repair. Plant Molecular Biology 1996, 31:585-593.
136. Machado C.R., Praekelt U.M., de Oliveira R.C., Barbosa A.C., Byrne K.L., Meacock P.A., Menck C.F. Dual role for the yeast THI4 gene in thiamine biosynthesis and DNA damage tolerance. Journal of Molecular Biology 1997, 273:114-121.
137. Makarchikov A.F., Lakaye B., Gulyai I.E., Czerniecki J., Coumans B., Wins P., Grisar T., Bettendorff L. Thiamine triphosphate and thiamine triphosphatase activities: From bacteria to mammals. Cellular and Molecular Life Science 2003, 60:1477-1488.
138. Malamy J., SanchezCasas P., Hennig J., Guo A.L., Klessig D.F. Dissection of the salicylic acid signaling pathway in tobacco. Molecular Plant-Microbe Interaction 1996, 9:474-482.
139. Marobbio C.M., Vozza A., Harding M., Bisaccia F., Palmieri F., Walker J.E. Identification and reconstitution of the yeast mitochondrial transporter for thiamine pyrophosphate. The EMBO Journal 2002, 21:5653-5661.
140. Martin P.R., Singleton C.K., Hiller-Sturmhöfel S. The role of thiamine deficiency in alcoholic brain disease. Alcohol Research and Health 2003, 27:134-142.
141. Martinez-Gomez N.C., Poyner R.R., Mansoorabadi S.O., Reed G.H., Downs D.M. Reaction of AdoMet with ThiC generates a backbone free radical. Biochemistry 2009, 48:217-219.
142. McCourt J.A., Duggleby R.G. Acetohydroxyacid synthase and its role in the biosynthetic pathway for branched-chain amino acids. Amino Acids 2006, 31:173-210.
143. McCourt J.A., Nixon P.F., Duggleby R.G. Thiamin nutrition and catalysis-induced instability of thiamin diphosphate. The British Journal of Nutrition 2006, 96:636-638.
144. McCulloch K.M., Kinsland C., Begley T.P., Ealick S.E. Structural studies of thiamin monophosphate kinase in complex with substrates and products. Biochemistry 2008, 47:3810-3821.
145. Miernyk J.A., Camp P.J., Randall D.D. Regulation of plant pyruvate dehydrogenase complexes. Current Topics in Plant Biochemistry and Physiology 1985, 4:175-190.
146. Miernyk J.A., Thelen J.J., Randall D.D. Reversible phosphorylation as a mechanism for regulating activity of the mitochondrial PDC. Plant Mitochondria: from Gene to Function 1998, 321-327. Leiden, The Netherlands, Backhuys Publishers. P. Gardestrom, I.M. Muller, K. Glimelius, E. Glaser (Eds.).
147. Millar A.H., Heazlewood J.L. Genomic and proteomic analysis of mitochondrial carrier proteins in Arabidopsis. Plant Physiology 2003, 131:443-453.
148. Millar A.H., Hill S.A., Leaver C.J. Plant mitochondrial 2-oxoglutarate dehydrogenase complex: Purification and characterization in potato. The Biochemical Journal 1999, 43:327-334.
149. Miranda-Ríos J. The THI-box riboswitch, or how RNA binds thiamin pyrophosphate. Structure 2007, 15:259-265.
150. Mironov A.S., Gusarov I., Rafikov R., Lopez L.E., Shatalin K., Kreneva R.A., Perumov D.A., Nudler E. Sensing small molecules by nascent RNA: A mechanism to control transcription in bacteria. Cell 2002, 111:747-756.
151. Mitsuda H., Takii Y., Iwami K., Yasumoto K., Nakajima K. Enzymatic formation of thiamine pyrophosphate in plants. Methods in Enzymology 1979, 62:107-111.
152. Mitsunaga T., Matsuda M., Shimizu M., Iwashima A. Isolation and properties of a thiamine-binding protein from buckwheat seed. Cereal Chemistry 1986, 63:332-335.
153. Mitsunaga T., Shimizu M., Iwashima A. Occurrence of thiamine-binding proteins in plant seeds. Journal of Plant Physiology 1986, 124:177-180.
154. Mitsunaga T., Shimizu M., Iwashima A. A possible role for thiamin-binding protein in the germination of rice seed. Journal of Plant Physiology 1987, 130:279-284.
155. Mizote T., Nakayama H. The thiM locus and its relation to phosphorylation of hydroxyethylthiazole in Escherichia coli. Journal of Bacteriology 1989, 171:3228-3232.
156. Mizote T., Truda M., Smith D.D., Nakayama H., Nakazawa T. Cloning and characterization of the thiD/J gene of Escherichia coli encoding a thiamin-synthesizing bifunctional enzyme, hydroxymethylpyrimidine kinase/phosphomethylpyrimidine kinase. Microbiology 1999, 145:495-501.
157. Molin W.T., Fites R.C. Isolation and characterization of thiamin hosphotransferase from Glycine max seedlings. Plant Physiology 1980, 66:308-312.
158. Molin W.T., Wilkerson C.G., Fites R.C. Thiamin phosphorylation by thiamin pyrophosphotransferase during seed germination. Plant Physiology 1980, 66:313-315.
159. Money B.P., Miernyk J.A., Randall D.D. The complex fate of alpha-ketoacids. Annual Review of Plant Biology 2002, 53:357-375.
160. Mozafar A., Oertli J.J. Uptake and transport of thiamin (vitamin-B1) by barley and soybean. Journal of Plant Physiology 1992, 139:436-442.
161. Mozafar A., Oertli J.J. Thiamin (vitamin-B(1))-Translocation and metabolism by soybean seedling. Journal of Plant Physiology 1993, 142:438-445.
162. Mücke U., König S., Hübner G. Purification and characterisation of pyruvate decarboxylase from pea seeds (Pisum sativum cv. Miko). Biological Chemistry Hoppe-Seyler 1995, 376:111-117.
163. Muhitch M.J., Shaner D.L., Stidham M.A. Imidazolinones and acetohydroxyacid synthase from higher plants: Properties of the enzyme from maize suspension culture cells and evidence for the binding of imazapyr to acetohydroxyacid synthase in vivo. Plant Physiology 1987, 83:451-456.
164. Müller C., Schwender J., Zeidler J., Lichtenthaler H.K. Properties and inhibition of the first two enzymes of the non-mevalonate pathway of isoprenoid biosynthesis. Biochemical Society Transactions 2000, 28:792-793.
165. Navarro D., Zwingmann C., Hazell A.S., Butterworth R.F. Brain lactate synthesis in thiamine deficiency: A re-evaluation using 1H-13C nuclear magnetic resonance spectroscopy. Journal of Neuroscience Research 2005, 79:33-41.
166. Nemeria N., Korotchkina L., McLeish M.J., Kenyon G.L., Patel M.S., Jordan F. Elucidation of the chemistry of enzyme-bound thiamin diphosphate prior to substrate binding: Defining internal equilibria among tautomeric and ionization states. Biochemistry 2007, 46:10739-10744.
167. Nghiêm H.O., Bettendorff L., Changeux J.P. Specific phosphorylation of Torpedo 43K rapsyn by endogenous kinase(s) with thiamine triphosphate as the phosphate donor. The FASEB Journal 2000, 14:543-554.
168. Nishimura M., Beevers H. Subcellular distribution of gluconeogenetic enzymes in germinating castor bean endosperm. Plant Physiology 1979, 64:31-37.
169. Nishimura H., Uehara Y., Sempuku K., Iwashima A. Purification and properties of thiamin-binding protein from rice bran. Journal of Nutritional Science and Vitaminology 1984, 30:1-10.
170. Nishino Y., Itokawa N., Nishino K., Piros J.R., Cooper J. Enzyme system involved in the synthesis of thiamin triphosphate. I. Purification and characterization of protein-bound thiamin diphosphate: ATP phosphoryltransferase. Journal of Biological Chemistry 1983, 258:11871-11878.
171. Nosaka K. Recent progress in understanding thiamin biosynthesis and its genetic regulation in Saccharomyces cerevisiae. Applied Microbiology and Biotechnology 2006, 72:30-40.
172. Nosaka K., Kaneko Y., Nishimura H., Iwashima A. Isolation and characterization of a thiamin pyrophosphokinase gene, THI80, from Saccharomyces cerevisiae. The Journal of Biological Chemistry 1993, 268:17440-17447.
173. Nosaka K., Nishimura H., Kawasaki Y., Tsujihara T., Iwashima A. Isolation and characterization of the THI6 gene encoding a bifunctional thiamin-phosphate pyrophosphorylase/hydroxyethylthiazole kinase from Saccharomyces cerevisiae. The Journal of Biological Chemistry 1994, 269:30510-30516.
174. Okuzaki A., Shimizu T., Kaku K., Kawai K., Toriyama K. A novel mutated acetolactate synthase gene conferring specific resistance to pyrimidinyl carboxy herbicides in rice. Plant Molecular Biology 2007, 64:219-224.
175. Ontiveros-Palacios N., Smith A.M., Grundy F.J., Soberon M., Henkin T.M., Miranda-Ríos J. Molecular basis of gene regulation by the THI-box riboswitch. Molecular Microbiology 2008, 67:793-803.
176. Ott K.H., Kwagh J.G., Stockton G.W., Sidorov V., Kakefuda G. Rational molecular design and genetic engineering of herbicide resistant crops by structure modeling and site-directed mutagenesis of acetohydroxyacid synthase. Journal of Molecular Biology 1996, 263:359-368.
177. Papini-Terzi F.S., Galhardo R.S., Farias L.P., Menck C.F., Van Sluys M.A. Point mutation is responsible for Arabidopsis tz-201 mutant phenotype affecting thiamin biosynthesis. Plant & Cell Physiology 2003, 44:856-860.
178. Paterami I., Kanellis A.K. Stress and developmental responses of terpenoid osynthetic genes in Cistus creticus subsp. creticus. Plant Cell Reports 2010, 29:629-641.
179. Paxton R., Scislowski P.W., Davis E.J., Harris R.A. Role of branched-chain 2-oxo acid dehydrogenase and pyruvate dehydrogenase in 2-oxobutyrate metabolism. The Biochemical Journal 1986, 234:295-303.
180. Peapus D.H., Chiu H.J., Campobasso N., Reddick J.J., Begley T.P., Ealick S.E. Structural characterization of the enzyme-substrate, enzyme-intermediate, and enzyme-product complexes of thiamin phosphate synthase. Biochemistry 2001, 40:10103-10114.
181. Peñuelas J., Munné-Bosch S. Isoprenoids: An evolutionary pool for photoprotection. Trends in Plant Science 2005, 10:166-169.
182. Phillips M.A., Walter M.H., Ralph S.G. Functional identification and differential expression of 1-deoxy-D-xylulose5-phosphate synthase in induced terpenoid resin formation of Norway Spruce (Picea abies). Plant Molecular Biology 2007, 65:243-257.
183. Raines C.A. The Calvin cycle revisited. Photosynthesis Research 2003, 75:1-10.
184. Integrative Medicine 2007, Saunders Elsevier, Philadelphia, PA. 2nd edn. D. Rakel (Ed.).
185. Ralser M., Wamelink M.M., Kowald A., Gerisch B., Heeren G., Struys E.A., Klipp E., Jakobs C., Breitenbach M., Lehrach H., Krobitsch S. Dynamic rerouting of the carbohydrate flux is key to counteracting oxidative stress. Journal of Biology 2007, 6:10.
186. Randall D.D., Miernyk J.A., David N.R., Gemel J., Luethy M.H. Regulation of leaf mitochondrial pyruvate dehydrogenase complex activity by reversible phosphorylation. Protein Phosphorylation in Plants 1996, 87-103. Oxford Press, Clarendon, UK. P.R. Shewry, N.G. Halford, R. Hooley (Eds.).
187. Rapala-Kozik M., Kozik A. Mechanism of ligand-protein interaction in plant seed thiamin-binding proteins. Probing the binding site of protein isolated from buckwheat seeds with a series of thiamin-related compounds. Biochimica et Biophysica Acta 1992, 1159:209-214.
188. Rapala-Kozik M., Kozik A. Mechanism of ligand-protein interaction in plant seed thiamine-binding proteins. Preliminary chemical identification of amino acid residues essential for thiamine binding to the buckwheat-seed protein. Biochimie 1996, 78:77-84.
189. Rapala-Kozik M., Kozik A. Purification and preliminary characterisation of a thiamine-binding protein from spruce seeds. Plant Physiology and Biochemistry 1998, 37:539-544.
190. Rapala-Kozik M., Chernikevich I.P., Kozik A. Ligand-protein interaction in plant seed thiamine-binding proteins. Binding of various thiamine analogues to the sepharose-immobilized buckwheat-seed protein. Journal of Protein Chemistry 1999, 18:721-728.
191. Rapala-Kozik M., Ostrowska K., Bednarczyk K., Duliński R., Kozik A. Polypeptide components of oligomeric legumin-like thiamin-binding protein from buckwheat seeds characterized by partial amino acid sequencing and photoaffinity labeling. Journal of Protein Chemistry 2003, 22:167-175.
192. Rapala-Kozik M., Olczak M., Ostrowska K., Starosta A., Kozik A. Molecular characterization of the thi3 gene involved in thiamine biosynthesis in Zea mays: cDNA sequence and enzymatic and structural properties of the recombinant bifunctional protein with 4-amino-5-hydroxymethyl-2-methylpyrimidine (phosphate) kinase and thiamine monophosphate synthase activities. The Biochemical Journal 2007, 408:149-159.
193. Rapala-Kozik M., Kowalska E., Ostrowska K. Modulation of thiamine metabolism in Zea mays seedlings under conditions of abiotic stress. Journal of Experimental Botany 2008, 59:4133-4143.
194. Rapala-Kozik M., Golda A., Kujda M. Enzymes that control the thiamine diphosphate pool in plant tissues. Properties of thiamine pyrophosphokinase and thiamine-(di)phosphate phosphatase purified from Zea mays seedlings. Plant Physiology and Biochemistry 2009, 47:237-242.
195. Raschke M., Burkle L., Muller N., Nunes-Nesi A., Fernie A.R., Arigoni D., Amrhein N., Fitzpatrick T.B. Vitamin B1 biosynthesis in plants requires the essential iron sulfur cluster protein, THIC. Proceedings of the National Academy of Sciences of the United States of America 2007, 104:19637-19642.
196. Reddick J.J., Nicewonger R., Begley T.P. Mechanistic studies on thiamin phosphate synthase: Evidence for a dissociative mechanism. Biochemistry 2001, 40:10095-10102.
197. Ribeiro A., Praekelt U., Akkermans A.D., Meacock P.A., van Kammen A., Bisseling T., Pawlowski K. Identification of agthi1, whose product is involved in biosynthesis of the thiamine precursor thiazole, in actinorhizal nodules of Alnus glutinosa. The Plant Journal 1996, 10:361-368.
198. Ribeiro D.T., Farias L.P., de Almeida J.D., Kashiwabara P.M., Ribeiro A.F., Silva-Filho M.C., Menck C.F., Van Sluys M.A. Functional characterization of the thi1 promoter region from Arabidopsis thaliana. Journal of Experimental Botany 2005, 56:1797-1804.
199. Ricci V., Rindi G. Thiamin uptake by rat isolated enterocytes: Relationship between transport and phosphorylation. Archives Internationales de Physiologie, de Biochimie et de Biophysique 1992, 100:275-279.
200. Rindi G., Laforenza U. Thiamine intestinal transport and related issues: Recent aspects. Proceedings of the Society for Experimental Biology and Medicine 2000, 224:246-255.
201. Rivoal J., Ricard B., Pradet A. Purification and partial characterization of pyruvate decarboxylase from Oryza sativa L. European Journal of Biochemistry 1990, 194:791-797.
202. Roche T.E., Baker J.C., Yan X., Hiromasa Y., Gong X., Peng T., Dong J., Turkan A., Kasten S.A. Distinct regulatory properties of pyruvate dehydrogenase kinase and phosphatase isoforms. Progress in Nucleic Acid Research and Molecular Biology 2001, 70:33-75.
203. Rodionov D.A., Vitreschak A.G., Mironov A.A., Gelfand M.S. Comparative genomics of thiamin biosynthesis in procaryotes. New genes and regulatory mechanisms. Journal of Biological Chemistry 2002, 277:48949-48959.
204. Rontein D., Dieuaide-Noubhani M., Dufourc E.J., Raymond P., Rolin D. The metabolic architecture of plant cells. Stability of central metabolism and flexibility of anabolic pathways during the growth cycle of tomato cells. Journal of Biological Chemistry 2002, 277:43948-43960.
205. Said H.M., Balamurug K., Subramanian V.S., Marchant J.S. Expression and functional contribution of hTHTR-2 in thiamin absorption in human intestine. American Journal of Physiology. Gastrointestinal and Liver Physiology 2004, 286:G491-G498.
206. Schenk G., Duggleby R.G., Nixon P.F. Properties and functions of the thiamin diphosphate dependent enzyme transketolase. The International Journal of Biochemistry & Cell Biology 1998, 30:1297-1318.
207. Schnarrenberger C., Flechner A., Martin W. Enzymatic evidence for a complete oxidative pentose phosphate pathway in chloroplasts and an incomplete pathway in the cytosol of spinach leaves. Plant Physiology 1995, 108:609-614.
208. Schroeder J.I., Nambara E. A quick release mechanism for abscisic acid. Cell 2006, 126:1023-1025.
209. Serganov A. Determination of riboswitch structures: Light at the end of the tunnel?. RNA Biology 2010, 7:98-103.
210. Serganov A., Polonskaia A., Phan A.T., Breaker R.R., Patel D.J. Structural basis for gene regulation by a thiamine pyrophosphate-sensing riboswitch. Nature 2006, 441:1167-1171.
211. Shaanan B., Chipman D.M. Reaction mechanisms of thiamin diphosphate enzymes: New insights into the role of a conserved glutamate residue. The FEBS Journal 2009, 276:2447-2453.
212. Shimamoto K., Nelson O.E. Movement of 14C-compounds from maternal tissue into maize seeds grown in vitro. Plant Physiology 1981, 67:429-432.
213. Shimizu M., Mitsunaga T., Inaba K., Yoshida T., Iwashima A. Accumulation of thiamine and thiamine-binding protein during development of rice seed. Journal of Plant Physiology 1990, 137:123-124.
214. Shimizu M., Inaba K., Yoshida T., Toda T., Iwashima A., Mitsunaga T. Purification and properties of thiamine-binding proteins from sesame seed. Physiologia Plantarum 1995, 93:93-98.
215. Shimizu T., Nakayama I., Nagayama K., Miyazawa T., Nezu Y. ALS inhibitors. Herbicide Classes in Development 2002, 1-41. Springer-Verlag, Berlin. P. Boeger, K. Wakabayashi, K. Hirai (Eds.).
216. Smith A.M., Fuchs R.T., Grundy F.J., Henkin T.M. Riboswitch RNAs: Regulation of gene expression by direct monitoring of a physiological signal. RNA Biology 2010, 7:104-110.
217. Song Q., Singleton C.K. Mitochondria from cultured cells derived from normal and thiamine-responsive megaloblastic anemia individuals efficiently import thiamine diphosphate. BMC Biochemistry 2002, 3:8.
218. Southan M.D., Copeland L. Physical and kinetic properties of acetohydroxyacid synthase from wheat leaves. Physiologia Plantarum 1996, 98:824-832.
219. Sprenger G.A., Schorken U., Wiegert T., Grolle S., De Graaf A.A., Taylor S.V., Begley T.P., Bringer-Meyer S., Sahm H. Identifcation of a thiamine-dependent synthase in Escherichia coli required for the formation of the 1-deoxy-D-xylulose 5-phosphate precursor to isoprenoids, thiamine and pyridoxol. Proceedings of the National Academy of Sciences of the United States of America 1997, 94:12857-12862.
220. Stepuro A.I., Piletskaya T.P., Stepuro I.I. Role of thiamine thiol form in nitric oxide metabolism. Biochemistry 2005, 70:339-349.
221. Sudarsan N., Barrick J.E., Breaker R.R. Metabolite-binding RNA domains are present in the genes of eukaryotes. RNA 2003, 9:644-647.
222. Sweetlove L.J., Heazlewood J.L., Herald V., Holtzapffel R., Day D.A., Leaver C.J., Millar A.H. The impact of oxidative stress on Arabidopsis mitochondria. The Plant Journal 2002, 32:891-904.
223. Tadege M., Dupuis I.I., Kuhlemeier C. Ethanolic fermentation: New functions for an old pathway. Trends in Plant Science 1999, 4:320-325.
224. Tallaksen C.M., Sande A., Bøhmer T., Bell H., Karlsen J. Kinetics of thiamin and thiamin phosphate esters in human blood, plasma and urine after 50mg intravenously or orally. European Journal of Clinical Pharmacology 1993, 44:73-78.
225. Tan S., Evans R.R., Dahmer M.L., Singh B.K., Shaner D.L. Imidazolinone-tolerant crops: History, current status and future. Pest Management Science 2005, 61:246-257.
226. Taylor N.L., Day D.A., Millar A.H. Targets of stress-induced oxidative damage in plant mitochondria and their impact on cell carbon/nitrogen metabolism. Journal of Experimental Botany 2004, 55:1-10.
227. Taylor N.L., Heazlewood J.L., Day D.A., Millar A.H. Lipoic acid-dependent oxidative catabolism of alpha-keto acids in mitochondria provides evidence for branched-chain amino acid catabolism in Arabidopsis. Plant Physiology 2004, 134:838-848.
228. Teige M., Kopriva S., Bauwe H., Süss K.H. Chloroplast pentose-5-phosphate 3-epimerase from potato: Cloning, cDNA sequence, and tissue-specific enzyme accumulation. FEBS Letter 1995, 377:349-352.
229. Teige M., Melzer M., Süss K.H. Purification, properties and in situ localization of the amphibolic enzymes D-ribulose 5-phosphate 3-epimerase and transketolase from spinach chloroplasts. European Journal of Biochemistry 1998, 252:237-244.
230. Thelen J.J., Miernyk J.A., Randall D.D. Partial purification and characterization of the maize mitochondrial pyruvate dehydrogenase complex. Plant Physiology 1998, 116:1443-1450.
231. Thompson P., Bowsher C.G., Tobin A.K. Heterogeneity of mitochondrial protein biogenesis during primary leaf development in barley. Plant Physiology 1998, 118:1089-1099.
232. Thore S., Leibundgut M., Ban N. Structure of the eukaryotic thiamine pyrophosphate riboswitch with its regulatory ligand. Science 2006, 312:1208-1211.
233. Thornalley P.J. The potential role of thiamine (vitamin B1) in diabetic complications. Current Diabetes Reviews 2005, 1:287-298.
234. Tittmann K., Golbik R., Uhlemann K., Khailova L., Schneider G., Patel M., Jordan F., Chipman D.M., Duggleby R.G., Hübner G. NMR analysis of covalent intermediates in thiamin diphosphate enzymes. Biochemistry 2003, 42:7885-7891.
235. Tovar-Méndez A., Miernyk J.A., Randall D.D. Regulation of pyruvate dehydrogenase complex activity in plant cells. European Journal of Biochemistry 2003, 270:1043-1049.
236. Trucco F., Hager A.G., Tranel P.J. Acetolactate synthase mutation conferring imidazolinone-specific herbicide resistance in Amaranthus hybridus. Journal of Plant Physiology 2006, 163:475-479.
237. Tunc-Ozdemir M., Miller G., Song L., Kim J., Sodek A., Koussevitzky S., Misra A.N., Mittler R., Shintani D. Thiamin confers enhanced tolerance to oxidativestress in Arabidopsis. Plant Physiology 2009, 151:421-432.
238. Valderrama R., Corpas F.J., Carreras A., Gómez-Rodríguez M.V., Chaki M., Pedrajas J.R., Fernández-Ocaña A., Del Río L.A., Barroso J.B. A dehydrogenase-mediated recycling of NADPH is a key antioxidant system against salt-induced oxidative stress in olive plants. Plant, Cell & Environment 2006, 29:1449-1459.
239. Vallabhaneni R., Wurtzel E.T. From epoxycarotenoids to ABA: The role of ABA 8'-hydroxylases in drought-stressed maize roots. Archives of Biochemistry and Biophysics 2010, 504:112-117.
240. Voskoboyev A.I., Ostrovsky Y.M. Thiamin pyrophosphokinase: Structure, properties, and role in thiamin metabolism. Annals of the New York Academy of Sciences 1982, 378:161-176.
241. Wachter A. Riboswitch-mediated control of gene expression in eukaryotes. RNA Biology 2010, 7:67-76.
242. Wachter A., Tunc-Ozdemir M., Grove B.C., Green P.J., Shintani D.K., Breaker R.R. Riboswitch control of gene expression in plants by splicing and alternative 3' end processing of mRNAs. The Plant Cell 2007, 19:3437-3450.
243. Wang D., Hazell A.S. Microglial activation is a major contributor to neurologic dysfunction in thiamine deficiency. Biochemical and Biophysical Research Communications 2010, 402:123-128.
244. Wang G., Ding X., Yuan M., Qiu D., Li X., Xu C., Wang S. Dual function of rice OsDR8 gene in disease resistance and thiamine accumulation. Plant Molecular Biology 2006, 60:437-449.
245. Webb E., Downs D. Characterization of thiL, encoding thiamin-monophosphate kinase, in Salmonella typhimurium. The Journal of Biological Chemistry 1997, 272:15702-15707.
246. WHO Thiamine deficiency and its prevention and control in major emergencies. Geneva, World Health Organization (WHO/NDH/99.13) 1999.
247. Widmann M., Radloff R., Pleiss J. The thiamine diphosphate dependent enzyme engineering database: A tool for the systematic analysis of sequence and structure relations. BMC Biochemistry 2010, 11:9.
248. Williams R.R., Cline J.K. Synthesis of vitamin B1. Journal of the American Chemical Society 1936, 58:1504-1505.
249. Williams M., Randall D.D. Pyruvate dehydrogenase complex from chloroplasts of Pisum sativum L. Plant Physiology 1979, 64:1099-1103.
250. Winkler W., Nahvi A., Breaker R.R. Thiamine derivatives bind messenger RNAs directly to regulate bacterial gene expression. Nature 2002, 419:952-956.
251. Wolak N., Kujda M., Banas A., Kozik A., Rapala-Kozik M. Involvement of thiamine (vitamin B1) in the response of Arabidopsis thaliana seedlings to the environmental stress. Acta Biochimica Polonica 2010, 57:112.
252. Wong C.E., Li Y., Labbe A., Guevara D., Nuin P., Whitty B., Diaz C., Golding G.B., Gray G.R., Weretilnyk E.A., Griffith M., Moffatt B.A. Transcriptional profiling implicates novel interactions between abiotic stress and hormonal responses in Thellungiella, a close relative of Arabidopsis. Plant Physiology 2006, 140:1437-1450.
253. Woodward J.B., Abeydeera N.D., Paul D., Phillips K., Rapala-Kozik M., Freeling M., Begley T.P., Ealick S.E., McSteen P., Scanlon M.J. A maize thiamine auxotroph is defective in shoot meristem maintenance. The Plant Cell 2010, 22:3305-3317.
254. Wynn R.M., Davie J.R., Meng M., Chuang D.T. In alpha -Ketoacid Dehydrogenase Complexes 1996, 101-117. Birkhauser Verlag, Basel. M.S. Patel, T.E. Roche, R.A. Harris (Eds.).
255. Yeaman S.J. The 2-oxo acid dehydrogenase complexes: Recent advances. The Biochemical Journal 1989, 257:625-632.
256. Yusa T. Thiamine triphosphate in yeasts and some plant materials. Plant & Cell Physiology 1961, 2:471-474.
257. Zabalza A., González E.M., Arrese-Igor C., Royuela M. Fermentative metabolism is induced by inhibiting different enzymes of the branched-chain amino acid biosynthesis pathway in pea plants. Journal of Agricultural and Food Chemistry 2005, 53:7486-9743.
258. Zeidler J., Sayer B.G., Spenser I.D. Biosynthesis of vitamin B1 in yeast. Derivation of the pyrimidine unit from pyridoxine and histidine. Intermediacy of urocanic acid. Journal of the American Chemical Society 2003, 125:13094-13105.
259. Zhang S.X., Weilersbacher G.S., Henderson S.W., Corso T., Olney J.W., Langlais P.J. Excitotoxic cytopathology, progression, and reversibility of thiamine deficiency-induced diencephalic lesions. Journal of Neuropathology and Experimental Neurology 1995, 54:255-267.
260. Zhang Y., Taylor S.V., Chiu H.J., Begley T.P. Characterization of the Bacillus subtilis thiC operon involved in thiamine biosynthesis. Journal of Bacteriology 1997, 179:3030-3035.
261. Zhang S., Zhou L., Nemeria N., Yan Y., Zhang Z., Zou Y., Jordan F. Evidence for dramatic acceleration of a C-H bond ionization rate in thiamin diphosphate enzymes by the protein environment. Biochemistry 2005, 44:2237-2243.
262. Zhang M., Li K., Zhang C., Gai J., Yu D. Identification and characterization of class 1 DXS gene encoding 1-deoxy-D-xylulose-5-phosphate synthase, the first committed enzyme of the MEP pathway from soybean. Molecular Biology Reports 2009, 36:879-887.
263. Zhao R., Gao F., Wang Y., Diaz G.A., Gelb B.D., Goldman I.D. Impact of the reduced folate carrier on the accumulation of active thiamin metabolites in murine leukemia cells. The Journal of Biological Chemistry 2001, 276:1114-11148.
264. Zhao R., Gao F., Goldman I.D. Reduced folate carrier transports thiamine monophosphate: An alternative route for thiamine delivery into mammalian cells. American Journal of Physiology. Cell Physiology 2002, 282:C1512-C1517.
265. Zhu J.K. Salt and drought stress signal transduction in plants. Annual Review of Plant Biology 2002, 53:247-273.