Evaluation of the antioxidant effects of carotenoids from Deinococcus radiodurans through targeted mutagenesis, chemiluminescence, and DNA damage analyses

Biochimica et Biophysica Acta - General Subjects

Volumn 1770, Issue 6, 2007, Pages 902-911

  Tian, Bing ^a   Xu, Zhenjian ^a   Sun, Zongtao ^a   Lin, Jun ^a   Hua, Yuejin ^a  

^a ZHEJIANG UNIVERSITY   (China)

Author keywords

Antioxidant effect; Carotenoids; Deinococcus radiodurans; Deinoxanthin; Phytoene synthase (CrtB); Reactive oxygen species

Indexed keywords

BETA CAROTENE; CAROTENOID; DEINOXANTHINE; HYDROGEN PEROXIDE; LYCOPENE; PHYTOENE SYNTHASE; REACTIVE OXYGEN METABOLITE; UNCLASSIFIED DRUG; XANTHOPHYLL; ZEAXANTHIN;

ANTIOXIDANT ACTIVITY; ARTICLE; CELL PROTECTION; CELL SURVIVAL; CHEMOLUMINESCENCE; CONTROLLED STUDY; DEINOCOCCUS RADIODURANS; DNA DAMAGE; DNA DETERMINATION; ENVIRONMENTAL STRESS; GENE MUTATION; MUTAGENESIS; NONHUMAN; PRIORITY JOURNAL;

BACTERIAL PROTEINS; CAROTENOIDS; CHEMILUMINESCENT MEASUREMENTS; DEHYDRATION; DEINOCOCCUS; DESICCATION; FREE RADICAL SCAVENGERS; GAMMA RAYS; GENE DELETION; GERANYLGERANYL-DIPHOSPHATE GERANYLGERANYLTRANSFERASE; HYDROGEN PEROXIDE; OXIDATIVE STRESS; SINGLET OXYGEN;

DEINOCOCCUS RADIODURANS;

EID: 34247226527     PISSN: 03044165     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.bbagen.2007.01.016     Document Type: Article

References (49)

1. Anderson A., Nordan H., Cain R., Parrish G., and Duggan D. Study on a radioresistant micrococcus: 1. Isolation, morphology, cultural characteristics, and resistant to γ-radiation. Food Technol. 10 (1956) 575-578
2. Wang P., and Schellhorn H.E. Induction of resistance to hydrogen peroxide and radiation in Deinococcus radiodurans. Can. J. Microbiol. 41 (1995) 170-176
3. Cox M.M., and Battista J.R. Deinococcus radiodurans-the consummate survivor. Nat. Rev. Microbiol. 3 (2005) 882-892
4. Venkateswaran A., Mcfarlan S.C., Ghosal D., Minton K.W., Vasilenko A., Makarova K., Wackett L.P., and Daly M.J. Physiologic determinants of radiation resistance in Deinococcus radiodurans. Appl. Environ. Microbiol. 66 (2000) 2620-2626
5. Daly M.J., Ouyang L., Fuchs P., and Minton K.W. In vivo damage and recA-dependent repair of plasmid and chromosomal DNA in the radiation-resistant bacterium Deinococcus radiodurans. J. Bacteriol. 176 (1994) 3508-3517
6. Battista J.R., Park M.J., and McLemore A.E. Inactivation of two homologous proteins presumed to be involved in the desiccation tolerance of plants sensitizes Deinococcus radiodurans R1 to desiccation. Cryobiology 43 (2001) 133-139
7. Kim J., Sharma A.K., Abbott S.N., Wood E.A., Dwyer D.W., Jambura A., Minton K.W., Inman R.B., Daly M.J., and Cox M.M. RecA protein from the extremely radioresistant bacterium Deinococcus radiodurans: expression, purification, and characterization. J. Bacteriol. 184 (2002) 1649-1660
8. Narumi I., Satoh K., Cui S., Funayama T., Kitayama S., and Watanabe H. PprA: a novel protein from Deinococcus radiodurans that stimulates DNA ligation. Mol. Microbiol. 54 (2004) 278-285
9. Narumi I. Unlocking radiation resistance mechanisms: still a long way to go. Trends Microbiol. 11 (2003) 422-425
10. Friedberg E.C., Walker G.C., and Siede W. DNA Repair and Mutagenesis (1995), ASM Press, Washington, DC 14-31
11. Ghosal D., Omelchenko M.V., Gaidamakova E.K., Matrosova V.Y., Vasilenko A., Venkateswaran A., Zhai M., Kostandarithes H.M., Brim H., Makarova K.S., Wackett L.P., Fredrickson J.K., and Daly M.J. How radiation kills cells: survival of Deinococcus radiodurans and Shewanella oneidensis under oxidative stress. FEMS Microbiol. Rev. 29 (2005) 361-375
12. Tian B., Wu Y., Sheng D., Zheng Z., Gao G., and Hua Y. Chemiluminescence assay for reactive oxygen species scavenging activities and inhibition on oxidative damage of DNA in Deinococcus radiodurans. Luminescence 19 (2004) 78-84
13. Markillie L.M., Varnum S.M., Hradecky P., and Wong K. Targeted mutagenesis by duplication insertion in the radioresistant bacterium Deinococcus radiodurans: radiation sensitivities of catalase (katA) and superoxide dismutase (sodA) mutants. J. Bacteriol. 181 (1999) 666-669
14. Daly M.J., Gaidamakova E.K., Matrosova V.Y., Vasilenko A., Zhai M., Venkateswaran A., Hess M., Omelchenko M.V., Kostandarithes H.M., Makarova K.S., Wackett L.P., Fredrickson J.K., and Ghosal D. Accumulation of Mn (II) in Deinococcus radiodurans facilitates gamma-radiation resistance. Science 306 (2004) 1025-1028
15. Fraser P.D., and Bramley P.M. The biosynthesis and nutritional uses of carotenoids. Prog. Lipid Res. 43 (2004) 228-265
16. Carbonneau M.A., Melin A.M., Perromat A., and Clerc M. The action of free radicals on Deinococcus radiodurans carotenoids. Arch. Biochem. Biophys. 275 (1989) 244-251
17. Hua Y., Narumi I., Gao G., Tian B., Satoh K., Kitayama S., and Shen B. PprI: a general switch responsible for extreme radioresistance of Deinociccus radiodurans. Biochem. Biophys. Res. Commun. 306 (2003) 354-360
18. Sheng D., Gao G., Tian B., Xu Z., Zheng Z., and Hua Y. RecX is involved in antioxidant mechanisms of the radioresistant bacterium Deinococcus radiodurans. FEMS Microbiol. Lett. 244 (2005) 251-257
19. Lemee L., Peuchant E., Clerc M., Brunner M., and Pfander H. Deinoxanthin: a new carotenoid isolated from Deinococcus radiodurans. Tetrahedron 53 (1997) 919-926
20. Gao G., Lu H., Huang L., and Hua Y. Construction of DNA damage response gene pprI function deficient and function complementary mutants in Deinococcus radiodurans. Chin. Sci. Bull. 50 (2005) 311-316
21. Giraud E., Hannibal L., Fardoux J., Jaubert M., Jourand P., Dreyfus B., Sturgis J.N., and Verméglio A. Two distinct crt gene clusters for two different functional classes of carotenoid in Bradyrhizobium. J. Biol. Chem. 279 (2004) 15076-15083
22. Misra H.S., Khairnar N.P., Kota S., Shrivastava S., Joshi V.P., and Apte S.K. An exonuclease I-sensitive DNA repair pathway in Deinococcus radiodurans: a major determinant of radiation resistance. Mol. Microbiol. 59 (2006) 1308-1316
23. Mattimore V., and Battista J.R. Radioresistance of Deinococcus radiodurans: functions necessary to survive ionizing radiation are also necessary to survive prolonged desiccation. J. Bacteriol. 178 (1996) 633-637
24. Lee G.Y., He D., Yu L., and Yu C. Identification of the ubiquinone-binding domain in QPs1 of succinate-ubiquinone reductase. J. Biol. Chem. 270 (1995) 6193-6198
25. Bradford M.M. A rapid and sensitive method for the quantification of microgram quantities of protein utilizing the principle of protein-dye binding. Anal. Biochem. 72 (1976) 248-254
26. Marklund S., and Marklund G. Assay of SOD by pyrogallol autooxidation. Eur. J. Biochem. 47 (1974) 469-474
27. Beers R.F., and Sizer I.W. A spectrophotometric method for measuring the breakdown of hydrogen peroxide by catalase. J. Biol. Chem. 195 (1952) 133-140
28. Deby-Dupont G., Deby C., Mouithys-Mickalad A., Hoebeke M., Mathy-Hartert M., Jadoul L., Vandenberghe A., and Lamy M. The antibiotic ceftazidime is a singlet oxygen quencher as demonstrated by ultra-weak chemiluminescence and by inhibition of AAP consumption. Biochim. Biophys. Acta 1379 (1998) 61-68
29. Yu W., and Zhao Y. Chemiluminescence evaluation of oxidative damage to biomolecules induced by singlet oxygen and the protective effects of antioxidants. Biochim. Biophys. Acta 1725 (2005) 30-34
30. Tian B., and Hua Y. Concentration dependence of prooxidant and antioxidant effects of aloin and aloe-emodin on DNA. Food Chem. 91 (2005) 413-418
31. Wang G., Hong Y., Johnson M.K., and Maier R.J. Lipid peroxidation as a source of oxidative damage in Helicobacter pylori: protective roles of peroxiredoxins. Biochim. Biophys. Acta 1760 (2006) 1596-1603
32. Bartley G.E., Viitanen P.V., Bacot K.O., and Scolnik P.A. A tomato gene expressed during fruit ripening encodes an enzyme of the carotenoid biosynthesis pathway. J. Biol. Chem. 267 (1992) 5036-5039
33. Akamine S., Nakamori K., Chechetka S.A., Banba M., Umehara Y., Kouchi H., Lzui K., and Hata S. cDNA cloning, mRNA expression, and mutational analysis of the squalene synthase gene of Lotus japonicus. Biochim. Biophys. Acta 1626 (2003) 97-101
34. Imlay J.A. Pathways of oxidative damage. Annu. Rev. Microbiol. 57 (2003) 395-418
35. Armstrong G.A., Alberti M., and Hearst J.E. Conserved enzymes mediate the early reactions of carotenoid biosynthesis in nonphotosynthetic and photosynthetic prokaryotes. Proc. Natl. Acad. Sci. U. S. A. 87 (1990) 9975-9979
36. Tao L., Picataggio S., Rouvière P.E., and Cheng Q. Asymmetrically acting lycopene β-cyclases (CrtLm) from non-photosynthetic bacteria. Mol. Genet. Genomics 271 (2004) 180-188
37. Hoshino T., Fujii R., and Nakahara T. Molecular cloning and sequence analysis of the crtB gene of Thermus thermophilus HB27, an extreme thermophile producing carotenoid pigments. Appl. Environ. Microbiol. 59 (1993) 3150-3153
38. Young A.J., and Lowe G.M. Antioxidant and prooxidant properties of carotenoids. Arch. Biochem. Biophys. 385 (2001) 20-27
39. Foote C.S., and Denny R.W. Chemistry of singlet oxygen: VIII. Quenching by β-Carotene. J. Am. Chem. Soc. 90 (1968) 6233-6235
40. Albrecht M., Takaichi S., Steiger S., Wang Z., and Sandmann G. Novel hydroxycarotenoids with improved antioxidative properties produced by gene combination in Escherichia coli. Nat. Biotechnol. 18 (2000) 843-846
41. Miller N.J., Sampson J., Candeias L.P., Bramley P.M., and Rice-Evans C.A. Antioxidant activities of carotenes and xanthophylls. FEBS Lett. 384 (1996) 240-242
42. Krinsky N.I., and Johnson E.J. Carotenoid actions and their relation to health and disease. Mol. Aspects Med. 26 (2005) 459-516
43. Krinsky N.I., Landrum J.T., and Bone R.A. Biologic mechanisms of the protective role of lutein and zeaxanthin in the eye. Annu. Rev. Nutr. 23 (2003) 171-201
44. Woodall A.A., Britton G., and Jackson M.J. Carotenoids and protection of phospholipids in solution or in liposomes against oxidation by peroxyl radicals: relationship between carotenoid structure and protective ability. Biochim. Biophys. Acta 1336 (1997) 575-586
45. Cantrell A., McGarvey D.J., Truscott T.G., Rancan F., and Böhm F. Singlet oxygen quenching by dietary carotenoids in a model membrane environment. Arch. Biochem. Biophys. 412 (2003) 47-54
46. Stahl W., Junghans A., Boer B., Driomina E.S., Briviba K., and Sies H. Carotenoid mixtures protect multilamellar liposomes against oxidative damage: synergistic effects of lycopene and lutein. FEBS Lett. 427 (1998) 305-308
47. Halliwell B. Oxygen and nitrogen are pro-carcinogens. Damage to DNA by reactive oxygen, chlorine and nitrogen species: measurement, mechanism and the effects of nutrition. Mutat. Res. 443 (1999) 37-52
48. Lavy A., Neeman Y., and Fuhrman B. The antioxidative effect of the bacteria Deinococcus radiophilus against LDL lipid peroxidation. Eur. J. Nutr. 44 (2005) 281-284
49. John Cram I.W., Zorn M., Wornik S., Yoshimura I., Stabentheiner E., and Pfeifhofer H.W. Antioxidants and photoprotection in a lichen as compared with its isolated symbiotic partners. Proc. Natl. Acad. Sci. U. S. A. 102 (2005) 3141-3146