Erratum: 5-Hydroxy-5,6-dihydro-apo-4,4′-lycopene and methyl 5-hydroxy-5,6-dihydro-apo-4,4′-lycopenoate, novel C 30-carotenoids produced by a mutant of marine bacterium Halobacillus halophilus (Journal of Antibiotics (2010) 63 (291-295) DOI: 10.1038/ja.2010.33);Hydroxy-3,4-dehydro-apo-8′-lycopene and methyl hydroxy-3,4-dehydro- apo-8′-lycopenoate, novel C 30 carotenoids produced by a mutant of marine bacterium Halobacillus halophilus

Journal of Antibiotics

Volumn 63, Issue 6, 2010, Pages 291-295

  Osawa, Ayako ^a   Ishii, Yoko ^a   Sasamura, Nao ^a   Morita, Marie ^a   Köcher, Saskia ^b   Müller, Volker ^b   Sandmann, Gerhard ^b   Shindo, Kazutoshi ^a  

^a JAPAN WOMEN'S UNIVERSITY   (Japan)

^b GOETHE UNIVERSITY   (Germany)

Author keywords

antioxidative activity; chemical mutagenesis; Halobacillus halophilus; hydroxy 3,4 dehydro apo 8 lycopene; methyl hydroxy 3,4 dehydro apo 8 lycopenoate

Indexed keywords

CAROTENOID; HYDROXY 3,4 DEHYDROAPO 8' LYCOPENE; METHYL GLUCOSYL 3,4 DEHYDROAPO 8' LYCOPENOATE; UNCLASSIFIED DRUG; ANTIOXIDANT; HYDROXY 3,4 DEHYDRO APO 8' LYCOPENE; HYDROXY-3,4-DEHYDRO-APO-8'-LYCOPENE; METHYL HYDROXY 3,4 DEHYDRO APO 8' LYCOPENOATE; METHYL HYDROXY-3,4-DEHYDRO-APO-8'-LYCOPENOATE;

ANTIOXIDANT ACTIVITY; ARTICLE; BACTERIUM MUTANT; CARBON NUCLEAR MAGNETIC RESONANCE; CHEMICAL MUTAGENESIS; DRUG ISOLATION; HALOBACILLUS HALOPHILUS; MARINE BACTERIUM; NONHUMAN; PHYSICAL CHEMISTRY; PRIORITY JOURNAL; PROTON NUCLEAR MAGNETIC RESONANCE; TAXONOMY; BACILLACEAE; DOSE RESPONSE; DRUG EFFECT; ISOLATION AND PURIFICATION; METABOLISM; MUTAGENESIS; NUCLEAR MAGNETIC RESONANCE; OXIDATION REDUCTION REACTION;

BACTERIA (MICROORGANISMS); HALOBACILLUS HALOPHILUS;

ANTIOXIDANTS; BACILLACEAE; CAROTENOIDS; DOSE-RESPONSE RELATIONSHIP, DRUG; MUTAGENESIS; NUCLEAR MAGNETIC RESONANCE, BIOMOLECULAR; OXIDATION-REDUCTION;

EID: 77954151611     PISSN: 00218820     EISSN: 18811469     Source Type: Journal    
DOI: 10.1038/ja.2014.53     Document Type: Erratum

References (15)

1. Goodwin, T. W. The Biochemistry of the carotenoids in Plant 2nd edn, Vol.1, 291-319 (Chapman and Hall: London, 1980).
2. Britton, G., Liaan-Jensen, S. & Pfander, H. Carotenoid Handbook (Birkhauser Verlag, Basel, 2004).
3. Nishino, H. et al. Cancer prevention by natural carotenoids. Biofactors 13, 89-94 (2000).
4. Iwamoto, T. et al. Inhibition of low-density lipoprotein oxidation by astaxanthin. J. Atherosclero. Throm. 7, 216-222 (2000).
5. Naito, Y. et al. Prevention of diabetic nephropathy by treatment with astaxanthin in diabetic db/db mice. Biofactors 20, 49-59 (2004).
6. Hosokawa, M. et al. Fucoxanthin induces apoptosis and enhances the antiproliferative effect of the PPAR gamma ligand, troglitazone, on colon cancer cells. Biochim. Biophys. Acta 1675, 113-119 (2004).
7. Shindo, K. et al. Rare carotenoid, (3R)-saproxanthin and (3R,2¢S)-myxol, isolated from novel marine bacteria (Flavobacteriaceae) and their antioxidative activities. Appl. Microbiol. Biotechnol. 74, 1350-1357 (2007).
8. Shindo, K. et al. Diapolycopenedioic acid xylosyl esters A, B, and C, novel glycol-C30- carotenoic acids produced by a new marine bacterium Rubritalea squalenifaciens. J. Antibiot. 61, 185-191 (2008).
9. Shindo, K. et al. Methyl glucosyl-3,4-dehydro-apo-8¢-lycopenoate, a novel antioxidative glyco-C30-carotenoic acid produced by a marine bacterium Planococcus maritimus. J. Antibiot. 61, 729-735 (2008).
10. Köcher, S., Breitenbach, J., Müller, V. & Sandmann, G. Structure, function and biosynthesis of carotenoids in the moderately halophilic bacterium Halobacillus halophilus. Arch. Microbiol. 191, 95-104 (2009).
11. Tao, L., Schenzle, A., Odom, J. M. & Cheng, Q. Novel carotenoid oxidase involved in biosynthesis of 4,4¢-diapolycopene dialdehyde. Appl. Environ. Microbiol. 71, 3294-3301 (2005).
12. Shimidzu, N., Goto, M. & Miki, W. Carotenoids as singlet oxygen quenchers in marine organisms. Fish. Sci. 62, 134-137 (1996).
13. Claus, D., Fahmy, F., Rolf, H. F. & Tosunoglu, N. Sporosarcina halophila sp. nov., an obligate slightly halophilic bacterium from salt marsh soils. Syst. Appl. Microbiol. 4, 496-506 (1983).
14. Kobayashi, M. & Sakamoto, Y. Singlet oxygen quenching ability of astaxanthin esters from the green alga Haematococcus pluvialis. Biotechol. Left. 21, 265-269 (1999).
15. Hirayama, O., Nakamura, K., Hamada, S. & Kobayashi, Y. Singlet oxygen quenching ability of naturally occurring carotenoids. Lipids 29, 149-150 (1994).