Native corrinoids from Clostridium cochlearium are adeninylcobamides:: Spectroscopic analysis and identification of pseudovitamin B12 and factor A

被引:35
作者
Hoffmann, B
Oberhuber, M
Stupperich, E
Bothe, H
Buckel, W
Konrat, R
Kräutler, B
机构
[1] Univ Innsbruck, Inst Organ Chem, A-6020 Innsbruck, Austria
[2] Univ Ulm, Inst Angew Mikrobiol, D-89069 Ulm, Germany
[3] Univ Marburg, Fachbereich Biol, Mikrobiol Lab, D-35032 Marburg, Germany
关键词
D O I
10.1128/JB.182.17.4773-4782.2000
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The corrinoids from the obligate anaerobe Clostridium cochlearium were extracted as a mixture of Cop-cyano derivatives. From 50 g of frozen cells, approximately 2 mg (1.5 mu mol) of B-12 derivatives was obtained as a crystalline sample. Analysis of the corrinoid sample of C. cochlearium by a combination of high-pressure liquid chromatography and W-Vis absorbance spectroscopy revealed the presence of three cyano corrinoids in a ratio of about 3:1:1. The spectroscopic data acquired for the sample indicated the main components to be pseudovitamin B-12(Co-beta-cyano-7 "-adeninylcobamide) (60%) and factor A (Co-beta-cyano-7 "- [2-methyl]adeninyl-cobamide) (20%). Authentic pseudovitamin B-12 was prepared by guided biosynthesis from cobinamide and adenine. Both pseudovitamin B-12 and its homologue, factor A, were subjected to complete spectroscopic analysis by W-Vis, circular dichroism, mass spectrometry, and by one- and two-dimensional H-1, C-13-, and N-15 nuclear magnetic resonance (NMR) spectroscopy. The third component was indicated by the mass spectra to be an isomer of factor A and is likely (according to NMR) to be 7 "- [N-6-methyl]-adeninylcobamide, a previously unknown corrinoid. C. cochlearium thus biosynthesizes as its native "complete" B-12 cofactors the 7 "-adeninyl-cobamides and two homologous corrinoids, in which the nucleotide base is a methylated adenine.
引用
收藏
页码:4773 / 4782
页数:10
相关论文
共 74 条
[1]  
Abend A, 1998, ANGEW CHEM INT EDIT, V37, P625, DOI 10.1002/(SICI)1521-3773(19980316)37:5<625::AID-ANIE625>3.0.CO
[2]  
2-4
[3]   A COENZYME CONTAINING PSEUDOVITAMIN B12 [J].
BARKER, HA ;
WEISSBACH, H ;
SMYTH, RD .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1958, 44 (11) :1093-1097
[4]   MLEV-17-BASED TWO-DIMENSIONAL HOMONUCLEAR MAGNETIZATION TRANSFER SPECTROSCOPY [J].
BAX, A ;
DAVIS, DG .
JOURNAL OF MAGNETIC RESONANCE, 1985, 65 (02) :355-360
[5]   H-1 AND C-13 ASSIGNMENTS FROM SENSITIVITY-ENHANCED DETECTION OF HETERONUCLEAR MULTIPLE-BOND CONNECTIVITY BY 2D MULTIPLE QUANTUM NMR [J].
BAX, A ;
SUMMERS, MF .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1986, 108 (08) :2093-2094
[6]   PRACTICAL ASPECTS OF TWO-DIMENSIONAL TRANSVERSE NOE SPECTROSCOPY [J].
BAX, A ;
DAVIS, DG .
JOURNAL OF MAGNETIC RESONANCE, 1985, 63 (01) :207-213
[7]   EVIDENCE FOR A MECHANISM INVOLVING TRANSIENT FRAGMENTATION IN CARBON SKELETON REARRANGEMENTS DEPENDENT ON COENZYME B-12 [J].
BEATRIX, B ;
ZELDER, O ;
KROLL, FK ;
ORLYGSSON, G ;
GOLDING, BT ;
BUCKEL, W .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 1995, 34 (21) :2398-2401
[8]   ESTIMATED RUMINAL PRODUCTION OF PSEUDO-VITAMIN B12 FACTOR-A AND FACTOR-B IN SHEEP [J].
BIGGER, GW ;
ELLIOT, JM ;
RICKARD, TR .
JOURNAL OF ANIMAL SCIENCE, 1976, 43 (05) :1077-1081
[9]   NATURAL ABUNDANCE N-15 NMR BY ENHANCED HETERONUCLEAR SPECTROSCOPY [J].
BODENHAUSEN, G ;
RUBEN, DJ .
CHEMICAL PHYSICS LETTERS, 1980, 69 (01) :185-189
[10]   Identification of the 4-glutamyl radical as an intermediate in the carbon skeleton rearrangement catalyzed by coenzyme B12-dependent glutamate mutase from Clostridium cochlearium [J].
Bothe, H ;
Darley, DJ ;
Albracht, SPJ ;
Gerfen, GJ ;
Golding, BT ;
Buckel, W .
BIOCHEMISTRY, 1998, 37 (12) :4105-4113