References
- J. Appl. Phycol. v.4 Microalgae aquaculture feeds Benemann,J.R. https://doi.org/10.1007/BF02161209
- Lipids v.24 Antioxidant activity of β-carotene-related carotenoids in solution Terao,J. https://doi.org/10.1007/BF02535085
- Arch. Biochem. Biophys. v.297 Astaxanthin and cathaxanthin are potent antioxidants in a membrane model Palozza,P.;N.I.Krinsky https://doi.org/10.1016/0003-9861(92)90675-M
- Biotechnol. Lett. v.21 Singlet oxygen quenching ability of astaxanthin esters from the green alga Haematococcus pluvialis Kobayashi,M.;Y.Sakamoto https://doi.org/10.1023/A:1005445927433
- Trends Biotechnol. v.21 Haematococcus astaxanthin: Applications for human health and nutrition Guerin,M.;M.E.Huntley;M.Olaizola https://doi.org/10.1016/S0167-7799(03)00078-7
- Crit. Rev. Biotechnol. v.11 Astaxanthin from microbial sources Johnson,E.A.;G.H.An https://doi.org/10.3109/07388559109040622
- J. Ferment. Bioeng. v.71 Astaxanthin production by a green alga, Haematococcus plusialis accompanied with morphological changes in acetate media Kobayashi,M.;T.Kakizono;S.Nagai https://doi.org/10.1016/0922-338X(91)90346-I
- Adv. Biochem. Eng. Biotechnol. v.53 Microbial carotenoids Johnson,E.A.;W.A.Schroeder
- J. Appl. Phycol. v.4 Algal carotenoids 51. Secondary carotenoids 2. Haematococcus pluvialis aplanospores as a source of (3S,3'S)-astaxanthin esters Grung,M.;F.M.L.D'Souza;M.Borowitzka;S.Liaaen-Jensen https://doi.org/10.1007/BF02442465
- J. Appl. Phycol. v.3 Culture of the astaxanthin-producing green alga Hamatococcus pluvialis: 1. Effect of nutrients on growth and cell type Borowitzka,M.A.;J.M.Huisman;A.Osborn https://doi.org/10.1007/BF02392882
- Plant Cell Physiol. v.32 Astaxanthin accumulation in the green alga Haematococcus pluvialis Boussiba,S.;A.Vonshak https://doi.org/10.1093/oxfordjournals.pcp.a078171
- J. Phycol. v.30 Cell cycle and accumulation of astaxanthin in Haematococcus lacustris (Chlorophyta) Lee,Y.K.;S.Y.Ding https://doi.org/10.1111/j.0022-3646.1994.00445.x
- J. Ferment. Bioeng. v.84 Morphological changes in the life cycle of the green alga Haematococcus pluvialis Kobayashi,M.;Y.Kurimura;T.Kakizono;N.Nishio;Y.Tsuji https://doi.org/10.1016/S0922-338X(97)82794-8
- Appl. Environ. Microbiol. v.59 Enhanced carotenoid biosynthesis by oxidative stress in acetate-induced cyst cells of a green unicelluloar alga, Haematococcus pluvialis Kobayashi,M.;T.Kakizono;S.Nagai
- J. Ferment. Bioeng. v.74 Effects of light intensity, light quality, and illumination cycle on astaxanthin formation in a green alga, Haematococcus pluvialis Kobayashi,M.;T.Kakizono;N.Nishio;S.Nagai https://doi.org/10.1016/0922-338X(92)90271-U
- Plant Growth Regul. v.22 Abscisic acid-dependent algal morphogenesis in the unicellular green alga Haematococcus pluvialis Kobayashi,M.;N.Hirai;Y.Kurimura;H.Ohigashi;Y.Tsuji https://doi.org/10.1023/A:1005862809711
- Biotechnol. Lett. v.19 Light independent astaxanthin production by the green microalga Haematococcus pluvialis under salt stress Kobayashi,M.;Y.Kurimura;Y.Tsuji https://doi.org/10.1023/A:1018372900649
- Biotechnol. Lett. v.16 Hyper-accumulation of astaxanthin in a green alga Haematococcus pluvialis at elevated temperatures Tjahjono,A.E.;Y.Hayama;T.Kakizono;Y.Terada;N.Nishio;S.Nagai https://doi.org/10.1007/BF01021659
- J. Gen. Microbiol. v.139 Antioxidant role of carotenoids in Phaffia rhodozyma Schroeder,W.A.;E.A.Johnson https://doi.org/10.1099/00221287-139-5-907
- Planta v.190 Are active oxygen species involved in induction of β-carotene in Dunaliella bardawil? Shaish,A.;M.Avron;U.Pick;A.Ben-Amotz
- Appl. Microbiol. Biotechnol. v.48 Antioxidant role of astaxanthin in the green alga Haematococcus pluvialis Kobayashi,M.;T.Kakizono;N.Nishio;S.Nagai;Y.Kurimura;Y.Tsuji https://doi.org/10.1007/s002530051061
- Appl. Microbiol. Biotechnol. v.54 In vivo antioxidant role of astaxanthin under oxidative stress in the green alga Haematococus pluvialis Kobayashi,M. https://doi.org/10.1007/s002530000416
- Protein, Nucleic Acid and Enzyme v.46 Algal carotenoid biosynthesis enhanced by active oxygen uner environmental stress Kobayashi,M.
- J. Ferment. Bioeng. v.74 Growth and astaxanthin formation of Haematococcus pluvialis in heterotriphic and mixotrophic conditions Kobayashi,M.;T.Kakizono;K.Yamaguchi;N.Nishio;S.Nagai https://doi.org/10.1016/0922-338X(92)90261-R
- Plant Pigments Biosynthesis of carotenoids Britton,G.;T.W.Goodwin(ed.)
- J. Biol. Chem. v.272 In vitro characterization of astaxanthin biosynthetic enzymes Fraser,P.D.;Y.Miura;N.Misawa https://doi.org/10.1074/jbc.272.10.6128
- Annu. Rev. Plant Physiol. Plant Mol. Biol. v.49 Genes and enzymes of carotenoid biosynthesis in plants Cunningham,F.X.;E.Gantt https://doi.org/10.1146/annurev.arplant.49.1.557
- Planta v.194 Drought induces oxidative stress in pea plants Moran,J.F.;M.Becana;I.Iturbe-Ormaetxe;S.Frechilla;R.V.Klucas;P.Aparicio-Tejo
- Free Rad. Res. Comms. v.8 Plants under drought-stress generate activated oxygen Price,A.H.;N.M.Atherton;G.A.F.Hendry https://doi.org/10.3109/10715768909087973
- Annu. Rev. Plant Physiol. Plant Mol. Biol. v.39 Metabolism and physiology of abscisic acid Zeevaart,J.A.D.;R.A.Creelman https://doi.org/10.1146/annurev.pp.39.060188.002255
- Bot. Acta v.102 Abscisic acid content of algae under stress Hirsch,R.;W.Hartung;H.Gimmler https://doi.org/10.1111/j.1438-8677.1989.tb00113.x
- Plant Cell Environ. v.26 Induction of tolerance to oxidative stress in the green alga, Chlamydomonas reinhardtii, by abscisic acid Yoshida,K.;E.Igarashi;M.Mukai;K.Hirata;K.Miyamoto https://doi.org/10.1046/j.1365-3040.2003.00976.x
- Physiol. Plant. v.83 The photoprotective role of carotenoids in higher plants Young,A.J. https://doi.org/10.1111/j.1399-3054.1991.tb02490.x
- Cytologia v.49 Ultrastructural study of Haematococcus lacustris (Girod.) Rostafinski (Volvocales): I. Some aspects of carotenogenesis Santos,M.F.;J.E.Mesquita https://doi.org/10.1508/cytologia.49.215
- Biotechnol. Lett. v.22 Protective role of astaxanthin against UV-B irradiation in the green alga Haematococcus pluvialis Kobayashi,M.;T.Okada https://doi.org/10.1023/A:1005649609839
- ACS Sym. Ser. v.637 Biotechnology of astaxanthin production in Phaffia rhodozyma Johnson,E.A.;W.A.Schroeder https://doi.org/10.1021/bk-1996-0637.ch004
- Lipids v.33 Rate constants for quenching singlet oxygen and activities for inhibiting lipid peroxidation of carotenoids and α-tocopherol in liposomes Fukuzawa,K.;Y.Inokami;A.Tokumura;J.Terao;A.Suzuki https://doi.org/10.1007/s11745-998-0266-y
- Fish. Sci. v.62 Carotenoids as singlet oxygen quenchers in marine organisms Simidzu,N.;M.Goto;W.Miki https://doi.org/10.2331/suisan.62.134
- Free Radicals in Biology and Medicine(2nd ed.) Halliwell,B.;J.M.C.Gutteridge
- J. Immunol. v.130 Flow cytometric studies of oxidative product formation by neutrophils: A graded response to membrane stimulation Bass,D.A.;J.W.Parce;L.R.Dechatelet;P.Szejda;M.C.Seeds;M.Thomas
- Physiol. Plant. v.94 Oxidative stress and antioxidant content in Chlorella vulgaris after exposure to ultraviolet-B radiation Malanga,G.;S.Puntarulo https://doi.org/10.1111/j.1399-3054.1995.tb00983.x
- J. Phycol. v.33 In vivo measurement of active oxygen production in the brown alga Fucus evanescens using 2',7'-dichlorohydrofluorescein diacetate Collen,J.;I.R.Davison https://doi.org/10.1111/j.0022-3646.1997.00643.x
- Eur. J. Biochem. v.223 carotenoid biosynthesis in microorganims and plants Sandmann,G. https://doi.org/10.1111/j.1432-1033.1994.tb18961.x
- J. Biotechnol. v.59 Metabolic engineering for the production of carotenoids in non-carotenogenic bacteria and yeasts Misawa,N.;H.Shimada https://doi.org/10.1016/S0168-1656(97)00154-5
- Appl. Microbiol. Biotechnol. v.51 Production of ketocarotenoids by microalgae Margalith,P.Z. https://doi.org/10.1007/s002530051413
- Physiol. Plant. v.108 Carotenogenesis in the green alga Haematococcus pluvialis: Cellular physiology and stress response Boussiba,S. https://doi.org/10.1034/j.1399-3054.2000.108002111.x
- FEBS Lett. v.500 Astaxanthin accumulation in Haematococcus requires a cytochrome P450 hydroxylase and an active synthesis of fatty acids Schoefs,B.;N.E.Rmiki;J.Rachadi;Y.Lemoine https://doi.org/10.1016/S0014-5793(01)02596-0
- Plant Mol. Biol. v.29 Isolation and functional identification of a novel cDNA for astaxanthin biosynthesis from Haematococcus pluvialis, and astaxanthin synthesis in Escherichia coli Kajiwara,S.;T.Kakizono;T.Saito;K.Kondo;T.Ohtani;N.Nishio;S.Nagai;N.Misawa https://doi.org/10.1007/BF00043657
- FEBS Lett. v.364 Cloning and expression in Escherichia coli of the gene encoding β-C-4-oxygenase, that converts β-carotene to the ketocarotenoid canthaxanthin in Haematococcus pluvialis Lotan,T.;J.Hirschberg https://doi.org/10.1016/0014-5793(95)00368-J
- Biochim. Biophys. Acta v.1446 Carotenoid hydroxylase from Haematococcus pluvialis: cDNA sequence, regulation and functional complementation Linden,H. https://doi.org/10.1016/S0167-4781(99)00088-3
- J. Biol. Chem. v.276 Ketocarotenoid biosynthesis outside o plastids in the unicellular green alga Haematococcus pluvialis Grunewald,K.;J.Hirschberg;C.Hagen https://doi.org/10.1074/jbc.M006400200
- Plant Physiol. v.125 Regulation of two carotenoid biosynthesis genes coding for phytoene synthase and carotenoid hydroxylase during stress-induced astaxanthin formation in the green alga Haematococcus pluvialis Steinbrenner,J.;H.Linden https://doi.org/10.1104/pp.125.2.810
- J. Biol. Chem. v.273 Induction and control of chromoplast-specific carotenoid genes by oxidative stress Bouvier,F.;R.A.Backhaus;B.Camara https://doi.org/10.1074/jbc.273.46.30651
- Eur. J. Biochem. v.233 Carotene desaturation is linked to a respiratory redox pathway in Narcissus pseudonarcissus chromoplast membranes: Involvement of a 23-kDa oxygen-evolving-complex-like protein Nievelstein,V.;J.Vandekerckhove;M.H.Tadros;J.V.Lintig;W.Nitschke;P.Beyer https://doi.org/10.1111/j.1432-1033.1995.864_3.x
- J. Phycol. v.31 Cytochrome f loss in astaxanthin-accumulating red cells of Haematococcus pluvialis (Chlorophyceae): Comparison of photosynthetic activity, photosynthetic enzymes, and thylakoid membrane polypeptides in red and green cells Tan,S.;F.X.Cunningham;M.Youmans;B.Grabowski;Z.Sun;E.Gantt https://doi.org/10.1111/j.0022-3646.1995.00897.x
- Plant Mol. Biol. v.52 Light induction of carotenoid biosynthesis genes in the green alga Haematococcus pluvialis: Regulation by photosynthetic redox control Steinbrenner,J.;H.Linden https://doi.org/10.1023/A:1023948929665
- J. Ferment. Bioeng. v.77 Isolation of resistant mutants against carotenoid biosynthesis inhibitors for a green alga Haematococcus pluvialis, and their hybrid formation by protoplast fusion for breeding of higher astaxanthin producers Tjahjono,A.E.;T.Kakizono;Y.Hayama;N.Nishio;S.Nagai https://doi.org/10.1016/0922-338X(94)90003-5
- Biotechnol. Lett. v.19 Isolation and characterization of compactin resistant mutants of an astaxanthin synthesizing green alga Haematococcus pluvialis Chumpolkulwong,N.;T.Kakizono;T.Handa;N.Nishio https://doi.org/10.1023/A:1018330329357
- World J. Microbiol. Biotechnol. v.17 Studies on Haematococcus pluvialis for improved production of astaxanthin by mutagenesis Tripathi,U.;G.Venkateshwaran;R.Sarada;G.A.Ravishankar https://doi.org/10.1023/A:1016609815405
- Biotechnol. Lett. v.25 Screening and characterization of astaxanthinhyperproducing mutants of Haematococcus pluvialis Chen,Y.;D.Li;W.Lu;J.Xing;B.Hui;Y.Han https://doi.org/10.1023/A:1022877703008
- J. Ferment. Bioeng. v.75 Formation and regeneration of protoplast from a unicellular green alga Haematococcus pluvialis Tjahjono,A.E.;T.Kakizono;Y.Hayama;S.Nagai https://doi.org/10.1016/0922-338X(93)90115-O
- J. Appl. Phycol. v.14 Transient expression of lacZ in bombarded unicellular green alga Haematococcus pluvialis Teng,C.;S.Qin;J.Liu;D.Yu;C.Liang;C.Tseng
- Biocatalysis v.1 Improved phycocatlysis of carotene production by flow cytometry and cell sorting Nonomura,A.M.;D.M.Coder https://doi.org/10.3109/10242428808998173
- J. Biosci. Bioeng. v.92 Enlarged and astaxanthin-accumulating cyst cells of the green alga Haematococcus pluvialis Kobayashi;M.T.Katsuragi;Y.Tani https://doi.org/10.1263/jbb.92.565
- Bio/Technol. v.9 Isolation and characterization of carotenoid hyperproducing mutants of yeast by flow cytometry and cell sorting An,G.H.;J.Bielich;R.Auerbach;E.A.Johnson https://doi.org/10.1038/nbt0191-70
- Plant Physiol. v.116 Induced β-carotene synthesis driven by triacylglycerol deposition in the unicellular alga Dunaliella bardawil Rabbani,S.;P.Beyer;J.von Lintig;P.Hugueney;H.Kleinig https://doi.org/10.1104/pp.116.4.1239
- Trends Biotechnol. v.18 Commercial potential for Haematococcus microalgae as a natural source of astaxanthin Lorenz,R.T.;G.R.Cysewski https://doi.org/10.1016/S0167-7799(00)01433-5
- J. Med. Food v.6 Safety of an astaxanthin-rich Haematococcus pluvialis algal extract: A randomized clinical trial Spiller,G.A.;A.Dewell https://doi.org/10.1089/109662003765184741
- Seibutsu-Kogaku v.80 Astaxanthin production by Haematococcus Kobayashi,M.