Sampson Edith M, Johnson Celeste L V, Bobik Thomas A
Department of Pediatrics, University of Florida, Gainesville, FL 32611, USA.
Department of Biochemistry, Biophysics and Molecular Biology, Iowa State University, Ames, IA 50011, USA.
Microbiology (Reading). 2005 Apr;151(Pt 4):1169-1177. doi: 10.1099/mic.0.27755-0.
Salmonella enterica degrades 1,2-propanediol (1,2-PD) by a pathway that requires coenzyme B(12) (adenosylcobalamin; AdoCbl). The genes specifically involved in 1,2-PD utilization (pdu) are found in a large contiguous cluster, the pdu locus. Earlier studies have indicated that this locus includes genes for the conversion of vitamin B(12) (cyanocobalamin; CNCbl) to AdoCbl and that the pduO gene encodes an ATP : cob(I)alamin adenosyltransferase which catalyses the terminal step of this process. Here, in vitro evidence is presented that the pduS gene encodes a bifunctional cobalamin reductase that catalyses two reductive steps needed for the conversion of CNCbl into AdoCbl. The PduS enzyme was produced in high levels in Escherichia coli. Enzyme assays showed that cell extracts from the PduS expression strain reduced cob(III)alamin (hydroxycobalamin) to cob(II)alamin at a rate of 91 nmol min(-1) mg(-1) and cob(II)alamin to cob(I)alamin at a rate of 7.8 nmol min(-1) mg(-1). In contrast, control extracts had only 9.9 nmol min(-1) mg(-1) cob(III)alamin reductase activity and no detectable cob(II)alamin reductase activity. Thus, these results indicated that the PduS enzyme is a bifunctional cobalamin reductase. Enzyme assays also showed that the PduS enzyme reduced cob(II)alamin to cob(I)alamin for conversion into AdoCbl by purified PduO adenosyltransferase. Moreover, studies in which iodoacetate was used as a chemical trap for cob(I)alamin indicated that the PduS and PduO enzymes physically interact and that cob(I)alamin is sequestered during the conversion of cob(II)alamin to AdoCbl by these two enzymes. This is likely to be important physiologically, since cob(I)alamin is extremely reactive and would need to be protected from unproductive by-reactions. Lastly, bioinformatic analyses showed that the PduS enzyme is unrelated in amino acid sequence to enzymes of known function currently present in GenBank. Hence, results indicate that the PduS enzyme represents a new class of cobalamin reductase.
肠炎沙门氏菌通过一条需要辅酶B12(腺苷钴胺素;AdoCbl)的途径降解1,2 - 丙二醇(1,2 - PD)。专门参与1,2 - PD利用的基因(pdu)位于一个大的连续基因簇即pdu位点中。早期研究表明,该位点包含将维生素B12(氰钴胺素;CNCbl)转化为AdoCbl的基因,并且pduO基因编码一种ATP:钴胺素(I)腺苷转移酶,该酶催化这一过程的最后一步。在此,提供了体外证据表明pduS基因编码一种双功能钴胺素还原酶,该酶催化将CNCbl转化为AdoCbl所需的两个还原步骤。PduS酶在大肠杆菌中大量产生。酶活性测定表明,来自PduS表达菌株的细胞提取物以91 nmol min⁻¹ mg⁻¹的速率将钴胺素(III)(羟基钴胺素)还原为钴胺素(II),并以7.8 nmol min⁻¹ mg⁻¹的速率将钴胺素(II)还原为钴胺素(I)。相比之下,对照提取物的钴胺素(III)还原酶活性仅为9.9 nmol min⁻¹ mg⁻¹,且未检测到钴胺素(II)还原酶活性。因此,这些结果表明PduS酶是一种双功能钴胺素还原酶。酶活性测定还表明,PduS酶将钴胺素(II)还原为钴胺素(I),以便由纯化的PduO腺苷转移酶转化为AdoCbl。此外,使用碘乙酸作为钴胺素(I)的化学捕获剂的研究表明,PduS和PduO酶在物理上相互作用,并且在这两种酶将钴胺素(II)转化为AdoCbl的过程中,钴胺素(I)被隔离。这在生理上可能很重要,因为钴胺素(I)具有极高的反应性,需要防止发生非生产性副反应。最后,生物信息学分析表明,PduS酶的氨基酸序列与GenBank中目前已知功能的酶无关。因此,结果表明PduS酶代表了一类新的钴胺素还原酶。