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PMID: 7651142 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

Helicobacter pylori nickel-transport gene nixA: synthesis of catalytically active urease in Escherichia coli independent of growth conditions.

Molecular microbiology ·Vol. 16 ·No. 1 ·1995-04-00 ·Pages 97-109

Mobley HL, Garner RM, Bauerfeind P

Abstract

Urease is a virulence determinant, a taxonomic and diagnostic marker, and immunogen for Helicobacter pylori, an aetiologic agent of gastritis and peptic ulceration. This enzyme requires Ni2+ ions in the active site for successful hydrolysis of urea. When expressed in Escherichia coli, recombinant urease is only weakly active unless urease structural subunits are overexpressed, exogenous NiCl2 is added, and the host strain is grown in medium that does not chelate free Ni2+. As wild-type H. pylori does not require such conditions for very high levels of urease expression, we reasoned that additional genes were required to accumulate the metal ion. To isolate such genes, E. coli SE5000 (pHP808), which carries the H. pylori urease gene cluster, was complemented with a lambda ZAP-derived plasmid library of the H. pylori chromosome. One of 1000 ampicillin-resistant clones, plated onto urea segregation agar, produced detectable urease. Urease activity of this co-transformant, grown in Luria broth containing 1 microM NiCl2, was 36 mumol NH3 min-1 mg-1 protein. Urease-enhancing activity, which is not directly linked to the urease gene cluster, was localized by subcloning and nucleotide sequencing. The largest open reading frame, designated nixA, predicted a polypeptide of 34,317 Da that displayed characteristics of an integral membrane protein. In vitro transcription-translation of nixA sequences yielded a polypeptide estimated to be 32 kDa in size. An in-frame Bal31 deletion within nixA abolished urease-enhancing activity. At 50 nM NiCl2, E. coli containing the nixA clone transported 1250 +/- 460 pmol Ni2+ min-1 10(-8) cells, whereas the vector control transported only 140 +/- 85 pmol Ni2+ min-1 10(8) cells, i.e. significantly less (P = 0.01). We conclude that NixA confers upon E. coli a high-affinity nickel-transport system (KT = 11.3 +/- 2.4 nM; Vmax = 1750 +/- 220 pmol Ni2+ min-1 10(-8) cells) and is necessary for expression of catalytically active urease, regardless of growth conditions.

Related Genes
MeSH Terms
Amino Acid Sequence Bacterial Proteins/genetics,metabolism Base Sequence Biological Transport Carrier Proteins/chemistry,genetics,metabolism Cation Transport Proteins Cloning, Molecular Culture Media Escherichia coli/genetics,growth & development,metabolism Genes, Bacterial Helicobacter pylori/genetics Kinetics Membrane Proteins/chemistry,genetics,metabolism Models, Biological Molecular Sequence Data Nickel/metabolism Restriction Mapping Sequence Alignment Sequence Deletion Urease/metabolism
Chemicals
Bacterial Proteins Carrier Proteins Cation Transport Proteins Culture Media Membrane Proteins NixA protein, Helicobacter pylori Nickel Urease
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Mobley H L
Department of Medicine, University of Maryland School of Medicine, Baltimore 21201, USA.
Garner R M
Bauerfeind P
Article Info
Journal
Molecular microbiology
Abbr.
Mol Microbiol
ISSN
0950-382X
Published
1995-04-00
Pages
97-109
Language
English
Region
England
NLM ID
8712028
Subset
IM
Grants
NIAID NIH HHS · AI23328 · United States
Databases
GENBANK
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