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在嗜热自养甲烷杆菌中用维生素B12替代辅酶α-(5-羟基苯并咪唑基)钴胺素(因子III)。

Substitution of Co alpha-(5-hydroxybenzimidazolyl)cobamide (factor III) by vitamin B12 in Methanobacterium thermoautotrophicum.

作者信息

Stupperich E, Steiner I, Eisinger H J

出版信息

J Bacteriol. 1987 Jul;169(7):3076-81. doi: 10.1128/jb.169.7.3076-3081.1987.

Abstract

Methanobacterium thermoautotrophicum grown on mineral medium contains 120 nmol of Co alpha-(5-hydroxybenzimidazolyl)cobamides (derivatives of factor III) per g of dry cell mass as the sole cobamide. The bacterium assimilated several corrinoids and benzimidazole bases during autotrophic growth. The corrinoids were converted into factor III; however, after three transfers in 5,6-dimethylbenzimidazole (200 microM)-supplemented mineral medium, derivatives of factor III were completely replaced by derivatives of vitamin B12, which is atypical for methanogens. The total cobamide content of these cells and their growth rate were not affected compared with factor III-containing cells. Therefore, the high cobamide content rather than a particular type of cobamide is required for metabolism of methanogens. Derivatives of factor III are not essential cofactors of cobamide-containing enzymes from methanogenic bacteria, but they are the result of a unique biosynthetic ability of these archaebacteria. The cobamide biosynthesis include unspecific enzymes, which made it possible either to convert non-species-derived corrinoids into derivatives of factor III or to synthesize other types of cobamides than factor III. The cobamide biosynthesis is regulated by its end product. In addition, the uptake of extracellular cobamides is controlled, and the assimilated corrinoids regulate cellular cobamide biosynthesis.

摘要

在矿物培养基上生长的嗜热自养甲烷杆菌每克干细胞质量含有120 nmol的Coα-(5-羟基苯并咪唑基)钴胺素(因子III的衍生物),作为唯一的钴胺素。该细菌在自养生长过程中同化了几种类咕啉和苯并咪唑碱基。类咕啉被转化为因子III;然而,在补充了5,6-二甲基苯并咪唑(200 μM)的矿物培养基中传代三次后,因子III的衍生物完全被维生素B12的衍生物取代,这对于产甲烷菌来说是不典型的。与含有因子III的细胞相比,这些细胞的总钴胺素含量及其生长速率没有受到影响。因此,产甲烷菌的代谢需要高含量的钴胺素,而不是特定类型的钴胺素。因子III的衍生物不是产甲烷细菌含钴胺素酶的必需辅因子,但它们是这些古细菌独特生物合成能力的结果。钴胺素生物合成包括非特异性酶,这使得将非物种来源的类咕啉转化为因子III的衍生物或合成除因子III之外的其他类型的钴胺素成为可能。钴胺素生物合成受其终产物调节。此外,细胞对细胞外钴胺素的摄取受到控制,同化的类咕啉调节细胞内钴胺素的生物合成。

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Microbial synthesis of cobamides.
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