Noens Elke E E, Kaczmarek Michał B, Żygo Monika, Lolkema Juke S
Molecular Microbiology, Groningen Biomolecular Sciences and Biotechnology Institute, University of Groningen, Groningen, The Netherlands.
Molecular Microbiology, Groningen Biomolecular Sciences and Biotechnology Institute, University of Groningen, Groningen, The Netherlands
J Bacteriol. 2015 Nov;197(22):3545-53. doi: 10.1128/JB.00526-15. Epub 2015 Aug 31.
The arginine deiminase (ADI) pathway gene cluster in Lactococcus lactis contains two copies of a gene encoding an l-arginine/l-ornithine exchanger, the arcD1 and arcD2 genes. The physiological function of ArcD1 and ArcD2 was studied by deleting the two genes. Deletion of arcD1 resulted in loss of the growth advantage observed in the presence of high l-arginine in different growth media. Uptake of l-arginine and l-ornithine by resting cells was reduced to the low level observed for an ArcD1/ArcD2 double deletion mutant. Deletion of the arcD2 gene did not affect the growth enhancement, and uptake activities were slightly reduced. Nevertheless, recombinant expression of ArcD2 in the ArcD1/ArcD2 double mutant did recover the growth advantage. Kinetic characterization of ArcD1 and ArcD2 showed high affinities for both l-arginine and l-ornithine (Km in the micromolar range). A difference between the two transporters was the significantly lower affinity of ArcD2 for the cationic amino acids l-ornithine, l-lysine, and l-histidine. In contrast, the affinity of ArcD2 was higher for the neutral amino acid l-alanine. Moreover, ArcD2 efficiently translocated l-alanine, while ArcD1 did not. Both transporters revealed affinities in the mM range for agmatine, cadaverine, histamine, and putrescine. These amines bind but are not translocated. It is concluded that ArcD1 is the main l-arginine/l-ornithine exchanger in the ADI pathway and that ArcD2 is not functionally expressed in the media used. ArcD2 is proposed to function together with the arcT gene that encodes a putative transaminase and is found adjacent to the arcD2 gene.
The arginine deiminase (ADI) pathway gene cluster in Lactococcus lactis contains two copies of a gene encoding an l-arginine/l-ornithine exchanger, the arcD1 and arcD2 genes. The physiological function of ArcD1 and ArcD2 was studied by deleting the two genes. It is concluded that ArcD1 is the main l-arginine/l-ornithine exchanger in the ADI pathway. ArcD2 is proposed to function as a l-arginine/l-alanine exchanger in a pathway together with the arcT gene, which is found adjacent to the arcD2 gene in the ADI gene cluster.
乳酸乳球菌中的精氨酸脱亚氨酶(ADI)途径基因簇包含两个编码L-精氨酸/L-鸟氨酸交换蛋白的基因拷贝,即arcD1和arcD2基因。通过缺失这两个基因研究了ArcD1和ArcD2的生理功能。缺失arcD1导致在不同生长培养基中存在高浓度L-精氨酸时观察到的生长优势丧失。静息细胞对L-精氨酸和L-鸟氨酸的摄取降低到了ArcD1/ArcD2双缺失突变体所观察到的低水平。缺失arcD2基因不影响生长增强,摄取活性略有降低。然而,在ArcD1/ArcD2双突变体中重组表达ArcD2确实恢复了生长优势。ArcD1和ArcD2的动力学特征显示对L-精氨酸和L-鸟氨酸都具有高亲和力(Km在微摩尔范围内)。这两种转运蛋白之间的一个差异是ArcD2对阳离子氨基酸L-鸟氨酸、L-赖氨酸和L-组氨酸的亲和力显著较低。相反,ArcD2对中性氨基酸L-丙氨酸的亲和力较高。此外,ArcD2能有效地转运L-丙氨酸,而ArcD1则不能。两种转运蛋白对胍丁胺、尸胺、组胺和腐胺的亲和力都在毫摩尔范围内。这些胺类能结合但不能转运。得出的结论是,ArcD1是ADI途径中主要的L-精氨酸/L-鸟氨酸交换蛋白,并且ArcD2在所使用的培养基中没有功能表达。有人提出ArcD2与编码一种假定转氨酶的arcT基因一起发挥作用,arcT基因位于arcD2基因附近。
乳酸乳球菌中的精氨酸脱亚氨酶(ADI)途径基因簇包含两个编码L-精氨酸/L-鸟氨酸交换蛋白的基因拷贝,即arcD1和arcD2基因。通过缺失这两个基因研究了ArcD1和ArcD2的生理功能。得出的结论是,ArcD1是ADI途径中主要的L-精氨酸/L-鸟氨酸交换蛋白。有人提出ArcD2在一条途径中作为L-精氨酸/L-丙氨酸交换蛋白发挥作用,该途径与arcT基因一起,arcT基因在ADI基因簇中位于arcD2基因附近。