COFACTOR ROLE FOR 10-FORMYLDIHYDROFOLIC ACID

被引:33
作者
BAGGOTT, JE [1 ]
JOHANNING, GL [1 ]
BRANHAM, KE [1 ]
PRINCE, CW [1 ]
MORGAN, SL [1 ]
ETO, I [1 ]
VAUGHN, WH [1 ]
机构
[1] UNIV ALABAMA, DEPT CHEM, BIRMINGHAM, AL 35294 USA
关键词
D O I
10.1042/bj3081031
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
10-Formyl-7,8-dihydrofolic acid (10-HCO-H(2)folate) was prepared by controlled air oxidation of 10-formyl-5,6,7,8-tetrahydrofolic acid (10-HCO-H(4)folate). The UV spectra of the 10-HCO-H(2)folate preparation has lambda(max.) 234, 333 nm and lambda(min.) 301 nm at pH 7.4, and lambda(max.) 257, 328 nm and lambda(min.) 229, 307 nm at pH 1. H-1-NMR spectroscopy of 10-HCO-H(2)folate (in (H2O)-H-2; 300 MHz) suggested a pure compound and gave resonances for one formyl group proton, two protons on C-7 and C-9, and no evidence for a C-6 proton, which is consistent with the structure proposed. The spectral properties indicated that the 10-HCO-H,folate preparation is not appreciably contaminated with 10-HCO-H(4)folate, 5,10-methenyltetrahydrofolic acid (5,10-CH=H(4)folate) or 10-formylfolic acid (10-HCO-folate). The above data establish that the 10-HCO-H(2)folate prepared here is authentic. In contrast, a folate with a UV spectrum having lambda(max.) 272 nm and lambda(min.) 256 nm at pH 7, which was prepared by 2,6-dichloro-indophenol oxidation of 10-HCO-H(4)folate and reported to be 97% pure [Baram, Chabner, Drake, Fitzhugh, Sholar and Allegra (1988) J. Biol. Chem. 263, 7105-7111], is apparently not 10-HCO-H(2)folate. 10-HCO-H-2 folate is utilized by Jurkat-cell (human T-cell leukaemia) and chicken liver aminoimidazolecarboxamide ribonucleotide transformylase (AICAR T'ase; EC 2.1.2.3) in the presence of excess 5-aminoimidazole-4-carboxamide ribotide (AICAR) resulting in the appearance of approximately 1 mol of H(2)folate product for each mol of AICAR formylated. The present 10-HCO-H(2)folate preparation had a kinetic advantage over 10-HCO-H(4)folate resulting from a difference of approx. 5-fold in K-m values when both folates were used as cofactors for Jurkat-cell and rat bone marrow AICAR T'ase. No substantial kinetic advantage was observed using chicken liver AICAR T'ase. 10-HCO-H(2)folate had little or no activity with Jurkat-cell or chicken liver glycinamide ribonucleotide transformylase (GAR T'ase, EC 2.1.2.2). The existence in vivo of 10-HCO-H(2)folate is suggested in mammals by several reports of detectable amounts of radiolabelled 10-HCO-folate in bile and urine after administration of radiolabelled folic acid.
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页码:1031 / 1036
页数:6
相关论文
共 24 条
[1]   DIFFERENCES IN METHOTREXATE AND 7-HYDROXYMETHOTREXATE INHIBITION OF FOLATE-DEPENDENT ENZYMES OF PURINE NUCLEOTIDE BIOSYNTHESIS [J].
BAGGOTT, JE ;
MORGAN, SL ;
VAUGHN, WH .
BIOCHEMICAL JOURNAL, 1994, 300 :627-629
[2]   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
[3]  
BARAM J, 1988, J BIOL CHEM, V263, P7105
[4]   EFFECT OF AN IMPLANTED WALKER TUMOR ON METABOLISM OF FOLIC-ACID IN RAT [J].
BARFORD, PA ;
BLAIR, JA .
BRITISH JOURNAL OF CANCER, 1978, 38 (01) :122-129
[5]  
BLADDEY RL, 1984, FOLATES PTERINS, V1, P191
[6]  
BLADDEY RL, 1955, BIOCHEM J, V72, P707
[7]   DISMUTATION OF DIHYDROFOLATE BY DIHYDROFOLATE-REDUCTASE [J].
BLAKLEY, RL ;
COCCO, L .
BIOCHEMISTRY, 1984, 23 (11) :2377-2383
[8]  
ELO I, 1980, ANAL BIOCHEM, V189, P167
[9]   THE ENZYMES OF PURINE NUCLEOTIDE SYNTHESIS DENOVO [J].
FLAKS, JG ;
LUKENS, LN .
METHODS IN ENZYMOLOGY, 1963, 6 :52-95
[10]   DETECTION OF INHIBITION OF 5-AMINOIMIDAZOLE-4-CARBOXAMIDE RIBOTIDE TRANSFORMYLASE BY THIOINOSINIC ACID AND AZATHIOPRINE BY A NEW COLORIMETRIC ASSAY [J].
HA, TS ;
MORGAN, SL ;
VAUGHN, WH ;
ETO, I ;
BAGGOTT, JE .
BIOCHEMICAL JOURNAL, 1990, 272 (02) :339-342