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2014 | 63 | 1 |

Tytuł artykułu

Zeaxanthin biosynthesis by members of the genus Muricauda

Warianty tytułu

Języki publikacji

EN

Abstrakty

EN
Zeaxanthin, a C₄₀ xanthophyll carotenoid, has potential biological applications in nutrition and human health. In this study we characterized carotenoid composition in 5 taxonomically related marine bacterial isolates from the genus Muricauda. The pigment was characterized using high performance liquid chromatography (HPLC) and mass spectrometry, which confirmed the presence of all-trans-zeaxanthin. Muricauda strains produced zeaxanthin as a predominant carotenoid. M. flavescens JCM 11812T produced highest yield (4.4 ± 0.2 mg L⁻¹) when cultured on marine broth at 32°C for 72 h. This is the first report on the presence of zeaxanthin among the majority of species from the genus Muricauda.

Wydawca

-

Rocznik

Tom

63

Numer

1

Opis fizyczny

p.115-119,fig.,ref.

Twórcy

autor
  • Yenepoya Research Centre, Yenepoya University, Deralakatte, Mangalore-575018, Karnataka State, India
autor
  • Yenepoya Research Centre, Yenepoya University, Deralakatte, Mangalore-575018, Karnataka State, India
autor
  • Yenepoya Research Centre, Yenepoya University, Deralakatte, Mangalore-575018, Karnataka State, India

Bibliografia

  • Arun A.B., W.M. Chen, W.A. Lai, J.H. Chao, P.D. Rekha, F.T. Shen, S. Singh and C.C. Young. 2009. Muricauda lutaonensis sp. nov., a moderate thermophile isolated from a coastal hot spring. Int. J. Syst. Evol. Microbiol. 59: 2738–2742.
  • Asker D., T.S. Awad, T. Beppu and K. Ueda. 2012. Novel zeaxanthin-producing bacteria isolated from radioactive hot spring water. Methods Mol. Biol. 892: 99–131.
  • Asker D., T. Beppu and K. Ueda. 2007(a). Mesoflavibacter zeaxanthinifaciens gen. nov., sp. nov., a novel zeaxanthin-producing marine bacterium of the family Flavobacteriaceae. Syst. Appl. Microbiol. 30: 291–296.
  • Asker D., T. Beppu and K. Ueda. 2007(b). Zeaxanthinibacter enoshimensis gen. nov., sp. nov., a novel zeaxanthin-producing marine bacterium of the family Flavobacteriaceae, isolated from seawater off Enoshima Island, Japan. Int. J. Syst. Evol. Microbiol. 57: 837–843.
  • Asker D., T. Beppu and K. Ueda. 2007(c). Sphingomonas jaspsi sp. nov., a novel carotenoid-producing bacterium isolated from Misasa, Tottori, Japan. Int. J. Syst. Evol. Microbiol. 57: 1435–1441.
  • Bhosale P. and P.S. Bernstein. 2004. Beta-carotene production by Flavobacterium multivorum in the presence of inorganic salts and urea. J. Ind. Microbiol. Biotechnol. 31: 565–571.
  • Bruns A., M. Rohde and L. Berthe-Corti. 2001. Muricauda ruestringensis gen. nov., sp. nov., a facultatively anaerobic, appendaged bacterium from German north sea intertidal sediment. Int. J. Syst. Evol. Microbiol. 51: 1997–2006.
  • Hameed A., A.B. Arun, H.P. Ho, C.M. Chang, P.D. Rekha, M.R. Lee, S. Singh and C.C. Young. 2011. Supercritical carbon dioxide micronization of zeaxanthin from moderately thermophilic bacteria Muricauda lutaonensis CC-HSB-11T. J. Agric. Food. Chem. 59: 4119–4124.
  • Hameed A., M. Shahina, S.Y. Lin, K.R. Sridhar, L.S. Young, M.R. Lee, W.M. Chen, J.H. Chou and C.C. Young. 2012. Siansivirga zeaxanthinifaciens gen. nov., sp. nov., a novel zeaxanthin-producing member of the family Flavobacteriaceae isolated from coastal seawater of Taiwan. FEMS Microbiol. Lett. 333: 37–45.
  • Huntemann M., H. Teshima, A. Lapidus, M. Nolan, S. Lucas, N. Hammon, S. Deshpande, J.F. Cheng, R. Tapia, L.A. Goodwin and others. 2012. Complete genome sequence of the facultatively anaerobic, appendaged bacterium Muricauda ruestringensis type strain B1T. Stand. Genomic. Sci. 6: 185–193.
  • Hwang C.Y., M.H. Kim, G.D. Bae, G.I. Zhang, Y.H. Kim and B.C. Cho. 2009. Muricauda olearia sp. nov., isolated from crude-oil-contaminated seawater, and emended description of the genus Muricauda. Int. J. Syst. Evol. Microbiol. 59: 1856–1861.
  • Kämpfer P., U. Dreyer, A. Neef, W. Dott and H.J. Busse. 2003. Chryseobacterium defluvii sp. nov., isolated from wastewater. Int. J. Syst. Evol. Microbiol. 53: 93–97.
  • Klassen J.L. 2009 Pathway evolution by horizontal transfer and positive selection is accommodated by relaxed negative selection upon upstream pathway genes in purple bacterial carotenoid biosynthesis. J. Bacteriol. 191: 7500–7508.
  • Klassen J.L. 2010. Phylogenetic and evolutionary patterns in microbial carotenoid biosynthesis are revealed by comparative genomics. PLoS ONE 5: 11257.
  • Krinsky N.I., J.T. Landrum and R.A. Bone. 2003. Biological mechanisms of the protective role of lutein and zeaxanthin in the eye. Annu. Rev. Nutr. 23: 171–201.
  • Lee S.Y., S. Park, T.K. Oh and J.H. Yoon. 2012. Muricauda beolgyonensis sp. nov., isolated from a tidal flat. Int. J. Syst. Evol. Microbiol. 62: 1134–1139.
  • Misawa N. 2011. Carotenoid β-ring hydroxylase and ketolase from marine bacteria promiscuous enzymes for synthesizing functional xanthophylls. Mar. Drugs 9: 757–771.
  • Sanusi R.A. and A.E. Adebiyi. 2009. Beta carotene content of commonly consumed foods and soups in Nigeria. Pak. J. Nutr. 8: 1512–1516.

Typ dokumentu

Bibliografia

Identyfikatory

Identyfikator YADDA

bwmeta1.element.agro-856e25e3-e734-4c00-a41e-f97ca1095aa2
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