Metabolism of 10-formyldihydrofolate in humans

被引:8
作者
Baggott, JE [1 ]
Tamura, T [1 ]
机构
[1] Univ Alabama, Dept Nutr Sci, Birmingham, AL 35294 USA
关键词
10-formyldihydrofolate; 10-formyltetrahydrofolate aminoimidazolocarboxamide ribotide; transformylase; humans; oxidation;
D O I
10.1016/S0753-3322(01)00093-2
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
The metabolism of 10-formyldihydrofolate is reviewed in this article. It had been the dogma that only tetra hydrofolates participate in enzyme-catalyzed one-carbon transfer reactions, until we showed in 1986 that 10-formyldihydrofolate serves as a substrate for aminoimidazolecarboxamide ribotide (AICAR) transformylase. Our data from studies in humans, cultured cells and bacteria as well as in vitro experiments indicate that the oxidation of 10-formyltetrahydrofolate to 10-formyldihydrofolate takes place, and 10-formyldihydrofolate is subsequently converted to dihydrofolate by AICAR transformylase. Dihydrofolate is then reduced to tetrahydrofolate and further metabolized by the well-established enzyme reactions. We believe that a new folate metabolic map is needed which incorporates the oxidation of 10-formyltetrahydrofolate and the utilization of 10-formyldihydrofolate by AICAR transformylase. (C) 2001 Editions scientifiques et medicales Elsevier SAS.
引用
收藏
页码:454 / 457
页数:4
相关论文
共 13 条
[1]   Bioactivity of orally administered unnatural isomers, [6R]-5-formyltetrahydrofolate and [6S]-5,10-methenyltetrahydrofolate, in humans [J].
Baggott, JE ;
Tamura, T .
BIOCHIMICA ET BIOPHYSICA ACTA-GENERAL SUBJECTS, 1999, 1472 (1-2) :323-332
[2]   10-Formyl-dihydrofolic acid is bioactive in human leukemia cells [J].
Baggott, JE ;
Johanning, GL .
JOURNAL OF NUTRITION, 1999, 129 (07) :1315-1318
[3]   Iron compounds catalyze the oxidation of 10-formyl-5,6,7,8-tetrahydrofolic acid to 10-formyl-7,8-dihydrofolic acid [J].
Baggott, JE ;
Robinson, CB ;
Eto, I ;
Johanning, GL ;
Cornwell, PE .
JOURNAL OF INORGANIC BIOCHEMISTRY, 1998, 71 (3-4) :181-187
[4]   Hydrolysis of 5,10-methenyltetrahydrofolate to 5-formyltetrahydrofolate at pH 2.5 to 4.5 [J].
Baggott, JE .
BIOCHEMISTRY, 2000, 39 (47) :14647-14653
[5]   COFACTOR ROLE FOR 10-FORMYLDIHYDROFOLIC ACID [J].
BAGGOTT, JE ;
JOHANNING, GL ;
BRANHAM, KE ;
PRINCE, CW ;
MORGAN, SL ;
ETO, I ;
VAUGHN, WH .
BIOCHEMICAL JOURNAL, 1995, 308 :1031-1036
[6]   Bioactivity of [6R]-5-formyltetrahydrofolate, an unnatural isomer, in humans and Enterococcus hirae, and cytochrome c oxidation of 10-formyltetrahydrofolate to 10-formyldihydrofolate [J].
Baggott, JE ;
Robinson, CB ;
Johnston, KE .
BIOCHEMICAL JOURNAL, 2001, 354 :115-122
[7]   INHIBITION OF 5-AMINOIMIDAZOLE-4-CARBOXAMIDE RIBOTIDE TRANSFORMYLASE, ADENOSINE-DEAMINASE AND 5'-ADENYLATE DEAMINASE BY POLYGLUTAMATES OF METHOTREXATE AND OXIDIZED FOLATES AND BY 5-AMINOIMIDAZOLE-4-CARBOXAMIDE RIBOSIDE AND RIBOTIDE [J].
BAGGOTT, JE ;
VAUGHN, WH ;
HUDSON, BB .
BIOCHEMICAL JOURNAL, 1986, 236 (01) :193-200
[8]   Re-evaluation of the metabolism of oral doses of racemic carbon-6 isomers of formyltetrahydrofolate in human subjects [J].
Baggott, JE ;
Tamura, T ;
Baker, H .
BRITISH JOURNAL OF NUTRITION, 2001, 85 (06) :653-657
[9]  
BAKER H, 1965, AM J CLIN NUTR, V17, P88, DOI 10.1093/ajcn/17.2.88
[10]   URINARY EXCRETION OF 5-METHYL-TETRAHYDROFOLATE IN MAN [J].
MCLEAN, A ;
CHANARIN, I .
BLOOD-THE JOURNAL OF HEMATOLOGY, 1966, 27 (03) :386-&