9.A.2.1.2 DabB2/DabA2 putative CO2 concentrating transporter, where DabB2 is a possible inorganic ion (H+ or Na+) transporter, homologous to integral membrane NADH dehydrogenase subunits, while DabA2 is homologous to carbonic anhydrases. Bacterial autotrophs often rely on CO2 concentrating
mechanisms (CCMs) to assimilate carbon. Desmarais et al. 2019 performed a genome-wide barcoded transposon screen to
identify essential and CCM-related genes in the γ-proteobacterium
Halothiobacillus neapolitanus. Screening revealed that the CCM comprises
at least 17 and probably no more than 25 genes, most of which are
encoded in 3 operons. Two of these operons (DAB1 and DAB2) contain a
two-gene locus that encodes a domain of unknown function (Pfam: PF10070)
and a putative cation transporter (Pfam: PF00361). Physiological and
biochemical assays demonstrated that these proteins (named DabA
and DabB for "DABs accumulate bicarbonate") - assemble into a heterodimeric
complex that contains a putative β-carbonic anhydrase-like active site
and functions as an energy-coupled inorganic carbon (Ci)
pump. DAB operons are found in a diverse range of
bacteria and archaea. Desmarais et al. 2019 demonstrated that functional DABs are present in
the human pathogens, Bacillus anthracis and Vibrio cholerae. They proposed that DABs constitute a class of
energized Ci pumps and play a critical role in the metabolism of Ci throughout prokaryotic phyla. Since the uptake of Ci is inhibited by the ionophore CCCP, DAB2 activity may be energetically coupled to a cation gradient, and as DabA2–DabB2 shows pH-independent rescue of carbonic anhydrase-free E. coli, CO2 is probably the transported substrate. Holthuijzen et al 1987 (DOI 10.1007/BF00463489) reported similar findings for Halothiobacillus neapolitanus, and (Menning et al. 2016) got similar results for Hydrogenovibrio crunogenus (Thiomicrospira crunogena). Both DAB operons in Halothiobacillus are required; each having an HCR phenotype when knocked out. A double deletion, which might be expected to have a more severe phenotype, was not constructed.
|
Accession Number: | D0KWS8 |
Protein Name: | NADH dehydrogenase (Quinone) |
Length: | 551 |
Molecular Weight: | 59136.00 |
Species: | Halothiobacillus neapolitanus (strain ATCC 23641 / c2) [555778] |
Number of TMSs: | 13 |
Location1 / Topology2 / Orientation3: |
Membrane1 / Multi-pass membrane protein2 |
Substrate |
hydrogencarbonate, carbon dioxide |
---|
1: MTIEFSHTTG LLLLAMPALL LMAAVIKPKQ GAAYARAYRQ RVQWTSFAAF GLALLAVVSF
61: LFARQQNLML GAGSLPAGLG LLALSIQVNG LTLVLASLVS FVLSVIARYS VQYLDGDPQQ
121: ARFFRLLAVT GGFFLLVVIS GNLGLFTLAI IATGFGLHRL LSFYADRPRA IMATHKKSIF
181: SRTADALLLA ATVLIGHQIG SLEFSQISAY VHAQDHLSIA LHVAAWLIVL AAILKSAQFP
241: FHGWLIQVME APTPVSALMH AGVVYSGAII VLRTSELLAA DGTALLLLAL IGLMTLAIGS
301: LVMLTQSAIK SSLAWSTAAQ LGFMMLELGL GLFGLALLHL VGHSLYKAHA FLSSGSMTDH
361: LRQAKVLKNR PISVVAWFTT VIVSGLFTLG IAAAMGLSID QEPMLPAVLT IIALATAQLM
421: LKALSHGTWR EILVAAGAAI AMTGVYVFLH EVFITGFADT LAATPQRAPL LDLLLMAITI
481: ITFLFVAWLQ GPGKTLMSPE RQFALFVHLN NGLYLDRWVE RLAFRFWPEK VGRAPKKSCA
541: VIPPNPSGIE P