Cation/proton antiporter complements of bacteria: why so large and diverse?
Cation/proton antiporter complements of bacteria: why so large and diverse?
复制标题
DOI:
10.1111/j.1365-2958.2009.06842.x
复制
发表时间:
2009-10
影响因子:
3.6
通讯作者:
Ito M
中科院分区:
文献类型:
--
作者:
Krulwich TA;Hicks DB;Ito M
Most bacterial genomes have 5–9 distinct genes predicted to encode transporters that exchange cytoplasmic Na+ and/or K+ for H+ from outside the cell, i.e. monovalent cation/proton antiporters. By contrast, pathogens that live primarily inside host cells usually possess 0–1 such antiporters while other stress-exposed bacteria exhibit even higher numbers. The monovalent cation/proton antiporters encoded by these diverse genes fall into at least eight different transporter protein families based on sequence similarity. They enable bacteria to meet challenges of high or fluctuating pH, salt, temperature or osmolarity, but we lack explanations for why so many antiporters are needed and for the value-added by specific antiporter types in specific settings. In this issue of Molecular Microbiology, analyses of the pH-dependence of cytoplasmic [Na+], [K+], pH and transmembrane electrical potential in the “poly-extremophile” Natranaerobius thermophilus are the context for assessment of the catalytic properties of 12 predicted monovalent cation/proton antiporters in the genome of this thermophilic haloalkaliphile. The results provide a profile of adaptations of the poly-extremophilic anaerobe, including a proposed role of cytoplasmic buffering capacity. They also provide new perspectives on two large monovalent cation/proton antiporter families, the NhaC and the Cation/Proton antiporter-3 (CPA3) antiporter families.
登录
查看更多内容
影响因子:
14.9
作者:
Ren Q;Chen K;Paulsen IT
通讯作者:
Paulsen IT
影响因子:
3.6
作者:
HAMAMOTO, T;HASHIMOTO, M;HORIKOSHI, K
通讯作者:
HORIKOSHI, K
影响因子:
14.9
作者:
Saier MH Jr;Tran CV;Barabote RD
通讯作者:
Barabote RD
影响因子:
3.6
作者:
Mesbah NM;Cook GM;Wiegel J
通讯作者:
Wiegel J
影响因子:
3.5
作者:
Mathiesen, C;Hägerhäll, C
通讯作者:
Hägerhäll, C