The DOI matches its Crossref record; 163 of the 163 references it cites were found in a registry or an index.
Nickel uptake and utilization by microorganisms
Open accessAbstract
Nickel is an essential nutrient for selected microorganisms where it participates in a variety of cellular processes. Many microbes are capable of sensing cellular nickel ion concentrations and taking up this nutrient via nickel-specific permeases or ATP-binding cassette-type transport systems. The metal ion is specifically incorporated into nickel-dependent enzymes, often via complex assembly processes requiring accessory proteins and additional non-protein components, in some cases accompanied by nucleotide triphosphate hydrolysis. To date, nine nickel-containing enzymes are known: urease, NiFe-hydrogenase, carbon monoxide dehydrogenase, acetyl-CoA decarbonylase/synthase, methyl coenzyme M reductase, certain superoxide dismutases, some glyoxylases, aci-reductone dioxygenase, and methylenediurease. Seven of these enzymes have been structurally characterized, revealing distinct metallocenter environments in each case.
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Cites
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Crystal structure of the nickel–iron hydrogenase from Desulfovibrio gigas
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Microbial ureases: significance, regulation, and molecular characterization.
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Self-citationMolecular biology of microbial ureases
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Self-citationClassification and phylogeny of hydrogenases
Vignais, P. (2001) · FEMS Microbiology Reviews · doi:10.1016/s0168-6445(01)00063-8 · Cited by 1,189
The protein–protein interaction map of Helicobacter pylori
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Self-citationStructure of the [NiFe] Hydrogenase Active Site: Evidence for Biologically Uncommon Fe Ligands
Volbeda, A., Garcin, E., Piras, C., de Lacey, A. L., Fernandez, V. M., Hatchikian, E. C., Frey, M., & Fontecilla-Camps, J. C. (1996) · Journal of the American Chemical Society · doi:10.1021/ja962270g · Cited by 673
Cited by
Rolfe, M. D., Rice, C. J., Lucchini, S., Pin, C., Thompson, A., Cameron, A. D. S., Alston, M., Stringer, M. F., Betts, R. P., Baranyi, J., et al. (2012) · Journal of Bacteriology · doi:10.1128/jb.06112-11 · Cited by 711
Lovley, D. R., Ueki, T., Zhang, T., Malvankar, N. S., Shrestha, P. M., Flanagan, K. A., Aklujkar, M., Butler, J. E., Giloteaux, L., Rotaru, A.-E., et al. (2011) · Advances in Microbial Physiology · doi:10.1016/b978-0-12-387661-4.00004-5 · Cited by 705
Coordination Chemistry of Bacterial Metal Transport and Sensing
Ma, Z., Jacobsen, F. E., & Giedroc, D. P. (2009) · Chemical Reviews · doi:10.1021/cr900077w · Cited by 621
New roles for bacterial siderophores in metal transport and tolerance
Schalk, I. J., Hannauer, M., & Braud, A. (2011) · Environmental Microbiology · doi:10.1111/j.1462-2920.2011.02556.x · Cited by 580
Nickel; whether toxic or essential for plants and environment - A review
Shahzad, B., Tanveer, M., Rehman, A., Cheema, S. A., Fahad, S., Rehman, S., & Sharma, A. (2018) · Plant Physiology and Biochemistry · doi:10.1016/j.plaphy.2018.10.014 · Cited by 403
Metadata
- Authors
- Mulrooney, S. B., & Hausinger, R. P.
- Venue
- FEMS Microbiology Reviews
- Publisher
- Oxford University Press (OUP)
- Published
- 2003-06
- Volume
- 27
- Issue
- 2-3
- Pages
- 239-261
- ISSN
- 0168-6445 (ISSN-L)
- 1574-6976
- OpenAlex
- W2099033590
- Cited by
- 516
- References
- 163
- FWCI
- 20.25
- Type
- journal article
- Language
- en
- Open access
- bronze
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Bibliographic data: Semantic Scholar, OpenAlex, Crossref.
Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
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