Acciarri Giuliana, Gizzi Fernán O, Torres Manno Mariano A, Stülke Jörg, Espariz Martín, Blancato Víctor S, Magni Christian
Laboratorio de Fisiología y Genética de Bacterias Lácticas, Instituto de Biología Molecular y Celular de Rosario (IBR), Sede Facultad de Ciencias Bioquímicas y Farmacéuticas (FBioyF), Universidad Nacional de Rosario (UNR), Consejo Nacional de Ciencia y Tecnología (CONICET), Rosario, Argentina.
Área Bioinformática, Departamento de Matemática y Estadística, Facultad de Ciencias Bioquímicas y Farmacéuticas, Universidad Nacional de Rosario, Rosario, Santa Fe, Argentina.
Front Microbiol. 2023 Feb 8;14:1117684. doi: 10.3389/fmicb.2023.1117684. eCollection 2023.
is able to grow in media at pH from 5.0 to 9.0 and a high concentration of NaCl (8%). The ability to respond to these extreme conditions requires the rapid movement of three critical ions: proton (H), sodium (Na), and potassium (K). The activity of the proton FF ATPase and the sodium Na VV type ATPase under acidic or alkaline conditions, respectively, is well established in . The potassium uptake transporters KtrI and KtrII were described in , which were associated with growth in acidic and alkaline conditions, respectively. In , the presence of the Kdp (potassium ATPase) system was early established. However, the homeostasis of potassium in this microorganism is not completely explored. In this study, we demonstrate that Kup and KimA are high-affinity potassium transporters, and the inactivation of these genes in . JH2-2 (a Kdp laboratory natural deficient strain) had no effect on the growth parameters. However, in KtrA defective strains (Δ, ΔΔ) an impaired growth was observed under stress conditions, which was restored to wild type levels by external addition of K ions. Among the multiplicity of potassium transporters identify in the genus , Ktr channels (KtrAB and KtrAD), and Kup family symporters (Kup and KimA) are present and may contribute to the particular resistance of these microorganisms to different stress conditions. In addition, we found that the presence of the Kdp system in . is strain-dependent, and this transporter is enriched in strains of clinical origin as compared to environmental, commensal, or food isolates.
能够在pH值为5.0至9.0以及高浓度氯化钠(8%)的培养基中生长。对这些极端条件作出反应的能力需要三种关键离子的快速移动:质子(H)、钠(Na)和钾(K)。质子FF ATP酶和钠Na VV型ATP酶在酸性或碱性条件下的活性分别在……中得到了充分证实。钾摄取转运蛋白KtrI和KtrII在……中被描述,它们分别与在酸性和碱性条件下的生长相关。在……中,早期就确定了Kdp(钾ATP酶)系统的存在。然而,这种微生物中钾的稳态尚未得到充分研究。在本研究中,我们证明Kup和KimA是高亲和力钾转运蛋白,并且在……中这些基因的失活。JH2-2(一种Kdp实验室天然缺陷菌株)对生长参数没有影响。然而,在KtrA缺陷菌株(Δ,ΔΔ)中,在应激条件下观察到生长受损,通过外部添加K离子可恢复到野生型水平。在……属中鉴定出的多种钾转运蛋白中,Ktr通道(KtrAB和KtrAD)以及Kup家族同向转运体(Kup和KimA)存在,并且可能有助于这些微生物对不同应激条件的特殊抗性。此外,我们发现……中Kdp系统的存在是菌株依赖性的,并且与环境、共生或食品分离株相比,该转运蛋白在临床来源的菌株中更为丰富。