The role of a 2-on-2 haemoglobin in oxidative and nitrosative stress resistance of Antarctic Pseudoalteromonas haloplanktis TAC125

Biochimie

Volumn 92, Issue 8, 2010, Pages 1003-1009

  Parrilli, Ermenegilda ^a   Giuliani, Maria ^a   Giordano, Daniela ^b   Russo, Roberta ^b   Marino, Gennaro ^a   Verde, Cinzia ^b   Tutino, Maria Luisa ^a  

^a UNIVERSITY OF NAPLES FEDERICO II   (Italy)

^b INSTITUTE OF PROTEIN BIOCHEMISTRY   (Italy)

Author keywords

Cold adapted bacteria; Oxygen scavenger; Pseudoalteromonas haloplanktis TAC125; Truncated haemoglobin

Indexed keywords

DISSOLVED OXYGEN; HYDROGEN PEROXIDE; TRUNCATED HEMOGLOBIN;

ARTICLE; BACTERIAL GROWTH; BACTERIAL PHENOMENA AND FUNCTIONS; BACTERIAL STRAIN; CONTROLLED STUDY; GENE INACTIVATION; MUTANT; NITROSATIVE STRESS; NONHUMAN; OXIDATIVE STRESS; OXYGEN TENSION; PROTEIN FUNCTION; PSEUDOALTEROMONAS; PSEUDOALTEROMONAS HALOPLANKTIS; TEMPERATURE; WILD TYPE;

AMINO ACID SEQUENCE; ANTARCTIC REGIONS; BASE SEQUENCE; DNA PRIMERS; GENES, BACTERIAL; HEMOGLOBINS; MODELS, MOLECULAR; MOLECULAR SEQUENCE DATA; MUTAGENESIS, INSERTIONAL; NITROSATION; OXIDATIVE STRESS; PSEUDOALTEROMONAS; REVERSE TRANSCRIPTASE POLYMERASE CHAIN REACTION; SEQUENCE HOMOLOGY, AMINO ACID;

BACTERIA (MICROORGANISMS); PSEUDOALTEROMONAS HALOPLANKTIS; VERTEBRATA;

EID: 77954660667     PISSN: 03009084     EISSN: 61831638     Source Type: Journal    
DOI: 10.1016/j.biochi.2010.04.018     Document Type: Article

References (30)

1. Methe B.A., Nelson K.E., Deming J.W., Momen B., Melamud E., Zhang X., Moult J., Madupu R., Nelson W.C., Dodson R.J., Brinkac L.M., Daugherty S.C., Durkin A.S., DeBoy R.T., Kolonay J.F., Sullivan S.A., Zhou L., Davidsen T.M., Wu M., Huston A.L., Lewis M., Weaver B., Weidman J.F., Khouri H., Utterback T.R., Feldblyum T.V., Fraser C.M. The psychrophilic lifestyle as revealed by the genome sequence of Colwellia psychrerythraea 34H through genomic and proteomic analyses. Proc. Natl. Acad. Sci. U. S. A. 2005, 102:10913-10918.
2. Rabus R., Ruepp A., Frickey T., Rattei T., Fartmann B., Stark M., Bauer M., Zibat A., Lombardot T., Becker I., Amann J., Gellner K., Teeling H., Leuschner W.D., Glockner F.O., Lupas A.N., Amann R., Klenk H.P. The genome of Desulfotalea psychrophila, a sulfate-reducing bacterium from permanently cold Arctic sediments. Environ. Microbiol. 2004, 6:887-902.
3. Médigue C., Krin E., Pascal G., Barbe V., Bernsel A., Bertin P.N., Cheung F., Cruveiller S., D'Amico S., Duilio A., Fang G., Feller G., Ho C., Mangenot S., Marino G., Nilsson J., Parrilli E., Rocha E.P.C., Rouy Z., Sekowska A., Tutino M.L., Vallenet D., von Heijne G., Danchin A. Coping with cold: the genome of the versatile marine Antarctica bacterium Pseudoalteromonas haloplanktis TAC125. Genome Res. 2005, 15:1325-1335.
4. Wittenberg J.B., Bolognesi M., Wittenberg B.A., Guertin M. Truncated haemoglobins: a new family of haemoglobins widely distributed in bacteria, unicellular eukaryotes and plants. J. Biol. Chem. 2002, 277:871-874.
5. Vinogradov S.N., Hoogewijs D., Bailly X., Arredondo-Peter R., Gough J., Dewilde S., Moens L., Vanfleteren J.R. A phylogenomic profile of globins. BMC Evol. Biol. 2006, 6:31-67.
6. Vuletich D.A., Lecomte J.T.J. A phylogenetic and structural analysis of truncated haemoglobins. J. Mol. Evol. 2006, 62:196-210.
7. Milani M., Pesce A., Nardini M., Ouellet H., Ouellet Y., Dewilde S., Bocedi A., Ascenzi P., Guertin M., Moens L., Friedman J.M., Wittenberg J.B., Bolognesi M. Structural bases for heme binding and diatomic ligand recognition in truncated haemoglobins. J. Inorg. Biochem. 2005, 99:97-109.
8. Ouellet H., Juszczak L., Dantsker D., Samuni U., Ouellet Y.H., Savard P.Y., Wittenberg J.B., Wittenberg B.A., Friedman J.M., Guertin M. Reactions of Mycobacterium tuberculosis truncated haemoglobin O with ligands reveal a novel ligand-inclusive hydrogen bond network. Biochemistry 2003, 42:5764-5774.
9. 2-binding haemoglobin from Mycobacterium tuberculosis. Proc. Natl. Acad. Sci. U. S. A. 1999, 96:11223-11228.
10. Frey A.D., Kallio P.T. Nitric oxide detoxification - a new era for bacterial globins in biotechnology?. Trends Biotechnol. 2005, 23:69-73.
11. Giordano D., Parrilli E., Dettaï A., Russo R., Barbiero G., Marino G., Lecointre G., di Prisco G., Tutino L., Verde C. The truncated haemoglobins in the Antarctic psychrophilic bacterium Pseudoalteromonas haloplanktis TAC125. Gene 2007, 398:69-77.
12. Parrilli E., Duilio A., Tutino M.L. Heterologous protein expression in psychrophilic hosts. Psychrophiles: from Biodiversity to Biotechnology 2008, 365-379. Springer-Verlag, Berlin Heidelberg. R. Margesin, F. Schinner, J.C. Marx, C. Gerday (Eds.).
13. Poole R.K. Nitric oxide and nitrosative stress tolerance in bacteria. Biochem. Soc. Trans. 2005, 33:176-180.
14. Molecular Cloning in a Laboratory Manual 2001, Cold Spring Harbor Laboratory, Cold Spring Harbor, NY. third ed. J. Sambrook, D.W. Russell (Eds.).
15. Papa R., Rippa V., Sannia G., Marino G., Duilio A. An effective cold inducible expression system developed in Pseudoalteromonas haloplanktis TAC125. J. Biotechnol. 2007, 127:199-210.
16. Ausubel F.M., Brent R., Kingston R.E., Moore D.D., Seidman J.G., Smith J.A., Struhl K. Current Protocols in Molecular Biology 1994, John Wiley & Sons, New York.
17. Parrilli E., De Vizio D., Cirulli C., Tutino M.L. Development of an improved Pseudoalteromonas haloplanktis TAC125 strain for recombinant protein secretion at low temperature. Microb. Cell Factories 2008, 7:2.
18. Tutino M.L., Parrilli E., Giaquinto L., Duilio A., Sannia G., Feller G., Marino G. Secretion of α-amylase from Pseudoalteromonas haloplanktis TAB23: two different pathways in different hosts. J. Bacteriol. 2002, 184:5814-5817.
19. Baillon M.L., van Vliet A.H., Ketley J.M., Constantinidou C., Penn C.W. An iron-regulated alkyl hydroperoxide reductase (AhpC) confers aerotolerance and oxidative stress resistance to the microaerophilic pathogen Campylobacter jejuni. J. Bacteriol. 1999, 181:4798-4804.
20. Hausladen A., Gow A.J., Stamler J.S. Nitrosative stress: metabolic pathway involving the flavohaemoglobin. Proc. Natl. Acad. Sci. U. S. A. 1998, 95:14100-14105.
21. Liu L., Zeng M., Hausladen A., Heitman J., Stamler J.S. Protection from nitrosative stress by yeast flavohaemoglobin. Proc. Natl. Acad. Sci. U. S. A. 2000, 97:4672-4676.
22. Spiro S. Regulators of bacterial responses to nitric oxide. FEMS Microbiol. Rev. 2007, 31:193-211.
23. Corker H., Poole R.K. Nitric oxide formation by Escherichia coli. Dependence on nitrite reductase, the NO-sensing regulator Fnr, and flavohaemoglobin Hmp. J. Biol. Chem. 2003, 278:31584-31592.
24. Ji X.B., Hollocher T.C. Reduction of nitrite to nitric oxide by enteric bacteria. Biochem. Biophys. Res. Commun. 1988, 157:106-108.
25. Lama A., Pawaria S., Bidon-Chanal A., Anand A., Gelpí J.L., Arya S., Martí M., Estrin D.A., Luque F.J., Dikshit K.L. Role of Pre-A motif in nitric oxide scavenging by truncated haemoglobin, HbN, of Mycobacterium tuberculosis. J. Biol. Chem. 2009, 284:14457-14468.
26. Giulivi C., Davies K.J. A novel antioxidant role for haemoglobin. The comproportionation of ferrylhaemoglobin with oxyhaemoglobin. J. Biol. Chem. 1990, 265:19453-19460.
27. Kvist M., Ryabova E.S., Nordlander E., Bülow L. An investigation of the peroxidase activity of Vitreoscilla haemoglobin. J. Biol. Inorg. Chem. 2007, 12:324-334.
28. Ouellet H., Ranguelova K., La Barre M., Wittenberg J.B., Wittenberg B.A., Magliozzo R.S., Guertin M. Reaction of Mycobacterium tuberculosis truncated haemoglobin O with hydrogen peroxide: evidence for peroxidatic activity and formation of protein-based radicals. J. Biol. Chem. 2007, 282:7491-7503.
29. 2 and NO scavenging by Mycobacterium leprae truncated haemoglobin O. Biochem. Biophys. Res. Commun. 2008, 373:197-201.
30. Feis A., Lapini A., Catacchio B., Brogioni S., Foggi P., Chiancone E., Boffi A., Smulevich G. Unusually strong H-bonding to the heme ligand and fast geminate recombination dynamics of the carbon monoxide complex of Bacillus subtilis truncated haemoglobin. Biochemistry 2008, 47:902-910.