The antioxidative function of eicosapentaenoic acid in a marine bacterium, Shewanella marinintestina IK-1

FEBS Letters

Volumn 581, Issue 22, 2007, Pages 4212-4216

  Nishida, Takanori ^a   Morita, Naoki ^b   Yano, Yutaka ^c   Orikasa, Yoshitake ^a   Okuyama, Hidetoshi ^a  

^a HOKKAIDO UNIVERSITY   (Japan)

^b NATIONAL INSTITUTE OF ADVANCED INDUSTRIAL SCIENCE AND TECHNOLOGY AIST   (Japan)

^c FISHERIES RESEARCH AGENCY   (Japan)

Author keywords

Eicosapentaenoic acid; Hydrogen peroxide; Oxidative stress; Protein carbonyl; Shewanella

Indexed keywords

HYDROGEN PEROXIDE; ICOSAPENTAENOIC ACID;

ANALYTIC METHOD; ANTIOXIDANT ACTIVITY; ARTICLE; BACTERIOSTASIS; CELL CULTURE; COLONY FORMING UNIT; CONTROLLED STUDY; MARINE BACTERIUM; NONHUMAN; OXIDATIVE STRESS; PRIORITY JOURNAL; PROTEIN CARBONYLATION; SHEWANELLA; SHEWANELLA MARININTESTINA; WILD TYPE;

ANTIOXIDANTS; CATALASE; COLONY COUNT, MICROBIAL; EICOSAPENTAENOIC ACID; FATTY ACIDS; HYDROGEN PEROXIDE; MUTATION; PROTEIN CARBONYLATION; SHEWANELLA;

BACTERIA (MICROORGANISMS); SHEWANELLA; SHEWANELLA MARININTESTINA;

EID: 34548127891     PISSN: 00145793     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.febslet.2007.07.065     Document Type: Article

References (22)

1. Nishida T., Orikasa Y., Ito Y., Yu R., Yamada A., Watanabe K., and Okuyama H. Escherichia coli engineered to produce eicosapentaenoic acid becomes resistant against oxidative damages. FEBS Lett. 580 (2006) 2731-2735
2. Nishida T., Orikasa Y., Watanabe K., and Okuyama H. The cell membrane-shielding function of eicosapentaenoic acid for Escherichia coli against exogenously added hydrogen peroxide. FEBS Lett. 580 (2006) 6690-6694
3. Okuyama H., Orikasa Y., Nishida T., Watanabe K., and Morita N. Bacterial genes responsible for the biosynthesis of eicosapentaenoic and docosahexaenoic acids and their heterologous expression. Appl. Environ. Microbiol. 73 (2007) 665-670
4. Hirota K., Nodasaka Y., Orikasa Y., Okuyama H., and Yumoto I. Shewanella pneumatophori sp. nov., an eicosapentaenoic acid-producing marine bacterium isolated from the intestines of pacific mackerel (Pneumatophorus japonicus). Int. J. Syst. Evol. Microbiol. 55 (2005) 2355-2359
5. Satomi M., Oikawa H., and Yano Y. Shewanella marinintestina sp. nov., Shewanella schlegeliana sp. nov. and Shewanella sairae sp. nov., novel eicosapentaenoic-acid-producing marine bacteria isolated from sea-animal intestines. Int. J. Syst. Evol. Microbiol. 53 (2003) 491-499
6. Alexeyev M.F. The pKNOCK series of broad-host-range mobilizable suicide vectors for gene knockout and targeted DNA insertion into the chromosome of Gram-negative bacteria. BioTechniques 26 (1999) 824-828
7. Fukuchi J., Sato T., Kato C., Ito M., and Horikoshi K. The host-vector system for deep-sea piezophilic bacteria, Shewanella violacea DSS12 and Moritella japonica DSK-1. JAMSTECR 46 (2002) 157-161 (in Japanese)
8. Levine R., Garland D., Oliver C.N., Amichi A., Climent I., Lenz A.-G., Ahn B.-W., Shaltiel S., and Estadtman R. Determination of carbonyl content in oxidatively modified proteins. Method Enzymol. 186 (1990) 464-478
9. Bradford M.M. A rapid and sensitive method for quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. Anal. Biochem. 14 (1976) 248-254
10. González-Flecha B., and Demple B. Intracellular generation of superoxide as a by-product of Vibrio harveyi luciferase expressed in Escherichia coli. J. Bacteriol. 176 (1994) 2293-2299
11. González-Flecha B., and Demple B. Homeostatic regulation of intracellular hydrogen peroxide concentration in aerobically growing Escherichia coli. J. Bacteriol. 179 (1997) 382-388
12. Pobiner H. Determination of hydrocarbon by conversion to hydrogen peroxide and measurement by titanium complexing. Anal. Chem. 33 (1961) 1423-1426
13. Orikasa Y., Nishida T., Hase A., Watanabe K., Morita N., and Okuyama H. A phosphopantetheinyl transferase gene essential for biosynthesis of n-3 polyunsaturated fatty acids from Moritella marina strain MP-1. FEBS Lett. 580 (2006) 4423-4429
14. Bligh E.G., and Dyer W.J. A rapid method of total lipid extraction and purification. Can. J. Biochem. Physiol. 37 (1959) 911-917
15. Okuyama H., Itoh H., Fukunaga N., and Sasaki S. Separation and properties of the inner and outer membranes of a psychrophilic bacterium, Vibrio sp. strain ABE-1. Plant Cell Physiol. 25 (1984) 1255-1264
16. Yumoto I., Yamazaki K., Kawasaki K., Ichise N., Morita N., Hoshino T., and Okuyama H. Isolation of Vibrio sp. S-1 exhibiting extraordinarily high catalase activity. J. Ferment. Bioeng. 85 (1999) 113-116
17. Allen E.E., Facciotti D., and Bartlett D.H. Monounsaturated but not polyunsaturated fatty acids are required for growth of the deep-sea bacterium Photobacterium profundum SS9 at high pressure and low temperature. Appl. Environ. Microbiol. 65 (1999) 1710-1720
18. Tamarit J., Cabiscol E., and Ros J. Identification of the major oxidatively damaged proteins in Escherichia coli cells exposed to oxidative stress. J. Biol. Chem. 273 (1998) 3027-3032
19. Weber H., Engelmann S., Becher D., and Hecker M. Oxidative stress triggers thiol oxidation in the glyceraldehyde-3-phosphate dehydrogenase of Staphylococcus aureus. Mol. Microbiol. 52 (2004) 133-140
20. Rajamoorthi K., Petrache H.I., McIntosh T.J., and Brown M.F. Packing and viscoelasticity of polyunsaturated omega-3 and omega-6 lipid bilayers as seen by (2)H NMR and X-ray diffraction. J. Am. Chem. Soc. 127 (2005) 1576-1588
21. Halliwell B., and Gutteridge J.M.C. Free Radicals in Biology and Medicine. third ed. (1998), Oxford University Press, Oxford
22. Ichise N., Morita N., Hoshino T., Kawasaki K., Yumoto I., and Okuyama H. A mechanism of resistance to hydrogen peroxide in Vibrio rumoiensis S-1. Appl. Environ. Microbiol. 65 (1999) 73-79