蓝藻与绿藻类胡萝卜素合成酶基因的比较基因组学及代谢调控研究
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摘要
类胡萝卜素在生物体内具有重要的生理功能,其中虾青素是一类高附加值值的类胡萝卜素。本文通过比较基因组学和实验手段,探索了类胡萝卜素相关基因的转录调控,为类胡萝卜素的代谢工程奠定的了基础。
     1、对已测序的18种蓝藻的类胡萝卜素合成基因进行了比较基因组学研究,发现除了Gloeobacter violaceus PCC 7421的类胡萝卜素合成途径是细菌型外,其余的蓝藻类胡萝卜合成途径均属于植物型。序列比对发现蓝藻中参与合成途径上游的酶基因在进化中保守性较高。研究还发现,一些类胡萝卜素合成酶在结构和功能上存在趋同或趋异进化,揭示它们进化上的多样性。
     2、通过比较基因组学分析,发现在集胞藻Synechocystis sp.PCC6803等几种蓝藻中,没有典型的番茄红素环化酶基因的同源基因,而存在着与绿硫细菌中的γ-carotene环化酶基因相似的基因,例如集胞藻中的sll0147和sll0659。但是研究结果显示sll0147和sll0659的突变对番茄红素环化过程影响不明显,提示在这些蓝藻中可能有其他基因参与环化过程,而sll0659基因可能参与了细胞的分裂过程。
     3、从经济绿藻雨生红球藻中克隆了参与类胡萝卜素合成途径的八氢番茄红素合成酶基因(psy)和八氢番茄红素脱氢酶基因(pds)的cDNA和基因组序列。通过基因组步移的方法克隆了这两个基因的5’侧翼序列,以本实验室建立的lacZ为报告基因的瞬间表达体系研究了这两个基因上游区域的启动子活性。
     4、通过ABA、N饥饿和高光诱导雨生红球藻积累虾青素,利用半定量RT-PCR方法分析了在相同环境因子诱导下雨生红球藻中类胡萝卜素合成基因的表达调控模式,结果显示在虾青素积累过程中,除了番茄红素环化酶基因变化不明显,其他一些基因均存在明显的转录上调。
     本研究首次利用比较基因组学的方法分析了类胡萝卜素基因的进化,发现大部分蓝藻的类胡萝卜合成途径属于植物型,一些类胡萝卜合成酶存在结构和功能的多样性。同时分离了雨生红球藻中类胡萝卜素相关基因八氢番茄红素合成酶基因(psy)和八氢番茄红素脱氢酶基因(pds)的5’上游侧翼序列,验证了它们的启动子功能,研究了雨生红球藻虾青素合成酶基因在相同环境因子诱导下的表达调控模式。本文将基础研究与实验验证相结合,为下一步研究类胡萝卜素合成的代谢工程提供了线索。
Caroteniods have many important physiological functions in organisms. Especially, astaxanthin has a high antioxidant activity, an anti-cancer activity, and other biological activities. This paper aims at the comparative genomics of the cyanobacterial carotenoid biosynthetic pathway. In addition, psy and pds were cloned and regulatory sequences were isolated and characterized in Haematococcus pluvialis. And also, expression patterns of crt gene were studied from Haematococcus pluvialis.
     Genome-wide screening of crt genes based on the genome-sequencing project provided us a new and comprehensive insight into the cyanobacterial carotenoid biosynthetic pathway. It is interesting to find that nearly all the cyanobacteria share quite similar pathway to synthesizeβ-carotene except for Gloeobacter violaceus PCC 7421 which is bacterial-type. The enzymes involved in the upstream pathway are more conserved than the subsequent ones. In addition, many carotenoid synthesis enzymes exhibit diversity in structure and function.
     Results of comparative genomics show there was not only no detectable crtL-e- but also no crtL-b-like lycopene cyclase gene in the genomes of Synechocystis sp. PCC6803 et al. However, there are homologous genes (sll0147 and sll0659,et al.) to a new type lycopene cyclase cruA from C. tepidum in these species. By genetical transformation system of Synechocystis sp.PCC6803, sll0147 and sll0659 which are similar to cruA were characterized. Full segregants of the sll0147 deletion in Synechocystis were not obtained, implying that this gene is essential for survival. The results of HPLC reveal these two enzymes have no lycopene cyclase activtity. However, the transmission electron micrographs showed that one major effect of the deletion is the abnormal phenotype, which suggests that sll0659 affects the cell division directly or indirectly.
     Phytoene synthease gene (psy) and phytoene desaturase gene (pds) were cloned from H. pluvialis. In addition, their 5'-flanking upstream sequences are obtained using adaptor-primer PCR method. The transient expressions of lacZ driven by psy 297bp and pds 210bp 5'-flanking sequence show that these sequences contain transcription regulatory sequences.
     In order to study the expression regulation, H.pluvialis was reduced by ABA, N starvation and high light. The expression patterns of crt genes were analysis by semi RT-PCR. The results showed all of genes were up-regulated except for lcy.
     This is the first report on the comparative genomics of carotenoid synthetic pathway of cyanobacteria and isolation of genomic genes and 5'flanking regions of psy and pds from H. pluvialis. This research provides a foundation for further study to finding new crt gene and the metabolic regulation of carotnoids.
引文
1. Abeles FB, Morgan PW and Saltveit ME Jr. Ethylene in Plant Biology. 1992, 2nd San Diego, CA, Academic Press.
    2. Alam BS, Alam SQ. The effect of different levels of dietary beta-carotene on DMBA-induced salivary gland tumors. Nutr Cancer. 1987, 9: 93-101.
    3. Albrecht M and Sandmann G. Light-stimulated carotenoid biosynthesis during transformation of maize etioplasts is regulated by increasedActivity of isopentenyl pyrophosphate isomerase. Plant Physiol. 1994, 105(2): 529-534.
    4. Altermann W, Kazmierczak J. Archean microfossils: a reappraisal of early life on Earth. Res Microbiol. 2003, 154:611-617.
    5. Altschul SF, Gish W, Miller W, Myers EW, Lipman DJ. Basic local alignment search tool. J Mol Biol. 1990, 215: 403-410.
    6. Anthony TD. Fat-soluble vitamins, their biochemistry and application. Trowbridge: Redwood Burn Ltd. 1985, 1-61.
    7. Armstrong GA, Alberti M, Hearst JE. Conserved enzymes mediate the early reactions of carotenoid biosynthesis in nonphotosynthetic and photosynthetic prokaryotes. Proc Natl Acad Sci, USA. 1990, 87: 9975-9979.
    8. Armstrong GA, Hearst JE. Carotenoids 2: genetics and molecular biology of carotenoid pigment biosynthesis.FASEB J. 1996, 10:228-237.
    9. Armstrong GA. Eubacteria showed their true colors: genetics of carotenoid pigment biosynthesis from microbes to plants. J Bacteriol. 1994, 176:4795-4802.
    10. Armstrong GA. Genetics of eubacterial carotenoid biosynthesis: a colorful tale. Annu Rev Microbiol. 1997, 51: 629- 659.
    11. Artus NN, Uemura M, Steponkus PL, et al. Constitutive expression of the cold-regulated Arabidopsis thaliana COR15a gene affects both chloroplast and protoplast freezing tolerance. Proc Natl Acad Sci, USA. 1996, 93:13404-13409.
    12. Bachmann A and Knust E. Dissection of cis-regulatory elements of the Drosophila gene Serrate. Dev Genes Evol. 1998, 208:346-351.
    13. Baker SS, Wilhelm KS, and Thomashow MF. The 5'-region of Arabidopsis thaliana cor15a has cis-acting elements that confer cold-, drought- and ABA-regulated gene expression. Plant Mol Biol.1994, 24:701-713.
    14. Barkley SJ, Desai SB, Poulter CD. Type II Isopentenyl Diphosphate Isomerase from Synechocystis sp. Strain PCC 6803. J Bacteriol. 2004, 186:8156-8158.
    15. Barros MD, Czarnecka E, Gurley WB. Mutational analysis of a plant heat shock element. Plant Mol Biol. 1992, 19: 665-675.
    16. Bartley GE, Scolnik PA, Beyer P. Two Arabidopsis thaliana carotene desaturases, phytoene desaturase and ζ-carotene desaturase, expressed in Escherichia coli, catalyze a poly-cis pathway to yield pro-lycopene. Eur J Biochem. 1999, 259:396-403.
    17. Bartley GE, Scolnik PA. cDNA cloning, expression during development, and genome mapping of PSY2, a second tomato gene encoding phytoene synthase. J Biol Chem. 1993, 268:25718-25721.
    18. Bartley GE, Scolnik PA. Plant carotenoids: Pigments for photoprotection, visual attractionand human health. Plant Cell. 1995, 7:1027-1038.
    19. Beems RB. The effect of beta-carotene on BP-induced respiratory tract tumors in hamsters.Nutr Cancer. 1987, 10(4):197-204.
    20. Bertram JS, Pung A, Churley M, Kappock TJ, Wilkins LR, Cooney RV. Diverse carotenoids protect against chemically induced neoplastic transformation. Carcinogenesis. 1991, 12:671-678.
    21. Bhaya D and Grossman AR. Characterization of gene clusters encoding the fucoxanthin chlorophylI proteins of the diatom Phaeodactylum tricorrutum.Nucleic Acid Res. 1993, 21(19): 4458-4466.
    22. Bidichandani SI, Ashizawa T, Patel PI. The GAA triplet-repeat expansion in Friedreich ataxia interferes with transcription and may be associated with an unusual DNA structure. Am J Hum Genet. 1998, 62(1):111-121.
    23. Bjerkeng B and Johnson G. Frozen storage quality of rainbow trout (Oncorkynchus mykiss) as affected by oxygen, illumination and fillet pigment. J Food Sci. 1995, 60(2):284-293.
    24. Bohne F, Linden H. Regulation of carotenoid biosynthesis genes in response to light inChlamydomonas reinhardtii. Biochim Biophys Acta. 2002, 1579(1):26-34.
    25. Bourdon V, Harvey A, Lonsdale DM. Introns and their positions affect the translational activity of mRNA in plant cells. EMBO Rep. 2001, 2:394-398.
    26. Boussiba S. Carotenogenesis in the green alga Haematococcus pluvialis: cellular physiology and stress response. Physiol Plant. 2000, 108(2):111-117.
    27. Bouvier F, d’Harlingue A, Hugueney P, Marin E, Marion-poll A, Camara B. Xanthophyll biosynthesis-cloning, expression, functional reconstitution, and regulation of beta-cyclohexenyl carotenoid epoxidase from pepper (Capsicum annuum). J Biol Chem. 1996, 271:28861-28867.
    28. Bowen WR. Ultrastructural aspects of the cell boundary of Haematococcus pluvialis. Trans Amer Microsc Soc. 1967, 86:36-43.
    29. Breitenbach J, Fernández-González B, Vioque A, Sandmann G. A higher-plant type ζ-carotene desaturase in the cyanobacterium Synechocystis PCC 6803. Plant Mol Biol. 1998, 36:725-732.
    30. Britton G, et a1.Carotenoids Handbook, Basel: Birkhauser Verlag,2004:VII
    31. Bryant DA.The molecular biology of cyanobacteria. Kluwer Academic publishers, 1996:559-579.
    32. Bub A, Watzl B, Abrahamse L, Delincee H, Adam S, Wever J, Muller H, Rechkemmer G. Moderate intervention with carotenoids-Rich vegetable products reduces lipid peroxidation in men. Nutr. 2000, 130:2000-2006.
    33. Buchman AR and Berg P. Comparison of intron-dependent and intron- independent gene expression. Mol Cell Biol. 1988, 8:4395-4405.
    34. Bujnicki JM. Understanding the evolution of restriction-modification systems: Clues from sequence and structure comparisons. Acta Biochim Pol. 2001, 48:935-967.
    35. Burja AM, Abou-Mansour E, Banaigs B, Payri C, Burgess JG and Wright PC. Culture of the marine cyanobacterium, Lyngbya majuscula (Oscillatoriaceae), for bioprocess intensified production of cyclic and linear lipopeptides. J Microbiol Methods. 2002, 48 (2-3):207-219.
    36. Callis J, Fromm M and Walbot V. Introns increase gene expression in cultured maize cells. Genes Dev. 1987, 1:1183-1200.
    37. Casey Es and Grossman A. In Vivo and In Vitro Characterization of theLight-Regulated cpcB2A2 Promoter of Fremyella diplosiphon.J Bacteriol.1994, 176(20): 6362-6374.
    38. Chamovitz D, Pecker I, Sandmann G, Boeger P, Hirschberg J. Cloning a gene for norflurazon resistance in cyanobacteria. Z Naturforsch. 1990, 45:482-486.
    39. Chenna R, Sugawara H, Koike T, Lopez R, Gibson TJ, Higgins DG, Thompson JD. Multiple sequences alignment with the clustal series of programs. Nucleic Acids Res. 2003, 31:3497-3500.
    40. Chew BP. Role of carotenoids in the immune response. J Dary Sci. 1993, 76:2804-2811.
    41. Chiou HC, Dabrowski C and Alwine JC. Simian virus 40 late mRNA leader sequences involved in augmenting mRNA accumulation via multiple mechanisms, including increased polyadenylation efficiency. J Virol. 1991, 65:6677-6685.
    42. Cornejo J, Willows RD and Beale SI. Phytobilin biosynthesis: cloning and expression of a gene encoding soluble ferredoxindependent heme oxygenase from Synechocystis sp. PCC 6803. Plant J. 1998, 15:99-107.
    43. Cowan AK, Rose PD. Abscisic acid metabolism in salt-stressed cells of Dunaliella salina. Plant Physiol. 1991, 97(2):798-803.
    44. Cunningham FX and Gantt E. Genes and enzymes of carotenoid biosynthesis in plants. Annu. Rev. Plant Physiol. Plant Mol Biol. 1998, 49:557-583.
    45. Cunningham FX and Gantt E. Identification of multi-gene families encoding isopentenyl diphosphate isomerase in plants by heterologous complementation in Escherichia coli. Plant and Cell Physiol. 2000, 41:119-123.
    46. Cunningham FX and Gantt E. One ring or two? Determination of ring number in caroteniods by lycopene epsilon-cylases. Proc Natl Acad Sci, USA. 2001, 98:2905-2910.
    47. Cunningham FX, Pogson B, Sun Z, McDonald KA, DellaPenna D, Gantt E. Functional analysisi of the beta and epsilon lycopene cylase enzyme of Arabidopsis reveals a mechanism for control of cyclic carotenoid formation. Plant Cell. 1996, 8:1613-1626.
    48. Cunningham FX, Sun Z, Chamovitz D, Hirschberg J, Gantt E. Molecular structure and enzymatic function of lycopene cylase from the cyanobacterium Synechococcus sp.strain PCC7942. Plant Cell. 1994, 6:1107-1121.
    49. Davoli P, Mierau V, Weber RWS. Carotenoids and fatty. acids in red yeasts Sporobolomyces roseus and Rhodotorula glutinis. Appl Biochem Microbiol. 2004, 40:392-397.
    50. Dawson HN, Burlingame R and Cannons A. Stable transformation of Chlorella: rescue of nitrate reductase deficient mutants with the nitrate reductase gene. Curr. Microbiol. 1997, 35:356-362.
    51. Demming-Adama B. Carotenoids and photoprotection in plants. A role for xanthophylls zeaxanthin. Biochim Biophys Acta. 1990, 1020:1-24.
    52. D?ring P, Treuter E, Kistner C, et al. Role of AHA motifs for the activator function of tomato heat stress transcription factors HsfA1 and HsfA2. Plant Cell. 2000, 12:265-278.
    53. Droop MR. Haematococcus pluvialis and its allies. Rev Alg N S. 1956, 2:53-71.
    54. Dufresne A, Salanoubat M, Partensky F, et al. Genome sequence of the cyanobacterium Prochlorococcus marinus SS120, a nearly minimal oxyphototrophic genome. Proc Natl Acad Sci, USA. 2003, 100(17):10020-10025.
    55. Duncker BP, Davies PL and Walker VK, Introns boost transgene expression in Drosophila melanogaster. Mol Gen Genet. 1997, 254:291-296.
    56. Elliott AM. Morphology and life history of Haematococcus pluvialis. Arch Protistenk. 1934, 82:250-272.
    57. Ershov Y, Gantt RR, Cunningham FX, Gantt E. Isopentenyl diphosphate isomerase dificiency in Synechocystis sp. Strain PCC6803. FEBS Lett. 2000, 473:337-34.
    58. Fernández-Gonzalez B, Sandmann G, Vioque A. A new type of asymmetrically acting β-carotene ketolase is required for the synthesis of echinenone in the cyanobacterium Synechocystis sp. PCC 6803. J Biol Chem. 1997, 272:9728-9733.
    59. Foyer CH and Harbinson J. Relationships between antioxidant metabolism and carotenoids in the regulation of photosynthesis. In: Frank HA, Yong AJ, Britton G, et al. The photochemistry of carotenoids. The Netherlands: Kluwer Academic pulisher, Dordrecht, 1999, 305-325.
    60. Fraser PD, Kiano JW, Truesdale M R, Schuch W, Bramley P M. Phytoene synthase-2 enzymes activity in tomato does not contribute to carotenoid synthesis in ripening fruit.Plant Mol Biol. 1999, 40:687-698.
    61. Fraser PD, Misawa N, Linden H, Shigeyuki Y, Kobayashi K, Sandmann G. Expression in E.coli, purification and reactivation of a recombinant Erwinia uredovora phytoene desaturase. J Biol Chem. 1992, 267:19891-19895.
    62. Fraser PD, Shimada H and Misawa N. Enzymic confirmation of reactions involved in routes to astaxathin formation, elucidated using a direct substrate in vitro assay. Eur J Biochem. 1998, 252:229-236.
    63. Frengova G, Simova E, Beshkova D. Use of whey ultrafiltrate as a substrate for production of carotenoids by the yeast Rhodotorula rubra. Appl Biochem Biotechnol. 2004, 12: 133-141.
    64. Frengova G, Simova E, Pavlova K, Beshkova D, Grigorova D. Formation of carotenoids by Rhodotorula glutinis in whey ultrafitrate. Biotechnol Bioeng. 1994, 44:888-894.
    65. Frigaard NU and Bryant DA. Seeing green bacteria in a new light: genomics-enabled studies of the photosynthetic apparatus in green sulfur bacteria and filamentous anoxygenic phototrophic bacteria. Archives of Microbiology. 2004, 182: 265-276.
    66. Fukuzawa K, Inokami Y, et al. Rate constants for quenching singlet oxygen and activities for inhibiting lipid peroxidation of carotenoids and α-tocopherol in liposomes. Lipids. 1998, 3: 751-756.
    67. Ganesh K, et al. An AU-box motif upstream of the SD sequence of light-dependent psbA transcripts confers mRNA instability in darkness in cyanobacteria. Nucleic Acids Res. 200, 29(9): 1835-1843.
    68. Grünewald K, Eckert M, Hirschberg J, Hagen C. Phytoene desaturase is localized exclusively in the chloroplast and up-regulated at the mRNA level during accumulation of secondary carotenoids in Haematococcus pluvialis (Volvocales, Chlorophyceae). Plant Physiol. 2000, 122:1261-1268.
    69. Gruss P, Lai CJ, et al., Splicing as a requirement for biogenesis of functional 16S mRNA of simian virus 40. Proc Natl Acad Sci. 1979, 76:4317-4321.
    70. Gruszecki WI, Strzajki K. Does the xanthophylls cycle take part in the regulation of fluidity of the thylakoid membranes? Biochem Biophysiol Acta. 1991, 1060:310-314.
    71. Hajela RK, Horvath DP, Gilmour SJ, et al. Molecular cloning and expression of cor(cold-regulated) genes in Arabidopsis thaliana. Plant Physiol. 1990, 93:1246-1252.
    72. Hao D, Ohme-Takagi M, Sarai A. Unique mode of GCC box recognition by the DNA-bindingdomain of ethylene-responsive element-binding factor (ERF domain) in plants. J Biol Chem. 1998, 273:26857-26861.
    73. Harker M and Young AJ. Inhibition of astaxanthin synthesis in the green alga, Haematococcus pluvialis. Eur J Phycol. 1995, 30(2):179-187.
    74. Harmer DH, Smith KD, et al. SV40 recombinants carrying rabbit -globin gene coding sequences. Cell. 1979, 17:725-735.
    75. Heerklotz D, D?ring P, Bonzelius F. The balance of nuclear import and export determines the intracellular distribution of tomato heat stress transcription factor HsfA2. Mol Cell Biol. 2001, 21:1759-1768.
    76. Heiser W. Optimization of biolistic transformation using the helium-driven PDS-1000/He system. US/EG Bull, 1688. Bio Rad, Hercules, CA, USA, 1992. pp (8).
    77. Hemmi H, Ikejiri S, Nakayama T, Nishino T. Fusion-type lycopene β-cylase from a thermoacidophilic archaeon Sulfolobus solfataricus. Biochem Biophys Res Comm. 2003, 305:586-591.
    78. Hess WR, Partensky F, Van der Staay GWM., Garcia-Fernandez JM, B?rner T, Vaulot D. Coexistence of phycoerythrin and a chlorophyll a/b antenna in a marine prokaryote. Proc Nat Acad Sci, USA. 1996, 93:11126-11130.
    79. Hieber AD, Bugos RC, Yamamoto HY. Plant lipocalins: violaxanthin de-epoxidase and zeaxanthin epoxidase. Biochim Biophys Acta. 2000, 1482:84-91.
    80. Higo K, Ugawa Y, Iwamoto M, et al. PLACE: a database of plant cis-acting regulatory DNA elements. Nucl Acid Res. 1998, 26:358-359.
    81. Hirsch R, Hartung W, Gimmler H, Abscisic acid content of algae under stress. Bot. Acta, 1989, 41:21-53.
    82. Hirschberg J. Carotenoid biosynthesis in flowering plants. Current Opinion in Plant Biology. 2001, 4:210-218.
    83. Hirschberg J. Molecular biology of carotenoid biosynthesis. In Carotenoids, vol 3.Edited by Britton G, Liaaen-Jensen S, Pfander H. Basel: Birkhauser verlag, 1998, pp: 149-194.
    84. Hischberg J,Cohen M,Harker M, Lotan T, Mann V, Pecker I. Molecular genetics of carotenoid biosynthesis pathway in plants and algae. Pure and Appl Chem. 1997, 69:2152-2158.
    85. Honda D, Yokota D, Sugiyama J. Detection of seven major evolutionary lineages in cyanobacteria based on the 16S rRNA gene sequence analysis with new sequences of five marine Synechococcus strains. J Mol Evol. 1999, 48:723-739.
    86. Huang JC, Chen F, Sandmann G. Stress-related differential expression of multiple beta-carotene ketolase genes in the unicellular green alga Haematococcus pluvialis. Journal of Biotechnology. 2006, 122(2):176-185.
    87. Hussein G, Sankawa U, Goto H, Matsumoto K and Watanabe H. Astaxanthin, a Carotenoid with Potential in Human Health and Nutrition. J Nat Prod. 2006, 69:443-449.
    88. Itoh T, Takemoto K, Mori H, Gojobori T. Evolutionary instability of operon structures disclosed by sequence comparisons of complete microbial genomes. Mol Biol Evol. 1999, 16:332-346.
    89. Jung HW, Lim CW, Hwang BK. Isolation and functional analysis of a pepper lipid transfer protein III (CALTPIII) gene promoter during signaling to pathogen, abiotic and environmental stresses. Plant Sci. 2006, 170(2):258-266.
    90. Kajiwara S, Fraser PD, Kondo K, Misawa N. Expression of an exogenous isopentenyl diphosphate isomerase gene enhances isoprenoid biosynthesis in Escherichia coli. Biochem J. 1997, 324:421-426.
    91. Kajiwara S, Kakizono T, Saito T, Kondo K, Ohtani T, Nishio N, Nagai S, et al. Isolation and functional identification of a novel cDNA for astaxantin biosynthesis from Haematococcus pluvialis, and astaxanthin synthesis in Escherichia coli. Plant Molecular Biology. 1995, 29(2):343-352.
    92. Kobayashi M, Kakizono T and Nagai S. Enhanced carotenoid biosynthesis by oxidative stress in acetate- induced cyst cells of a green unicellular alga, Haematococcus pluvialis. Appl Environ Microbiol.1993, 59(3):867-873.
    93. Konstantinidis KT and Tiedje JM. Trends between gene content and genome size in prokaryotic species with larger genomes. Proc Natl Acad Sci, USA. 2004,101:3160-3165.
    94. Krubasik P and Sandmann G. A carotengenic gene cluster form Brevibacterium linens with novel lycopene cyclase gene involved in the synthesis of aromatic carotenoids. Mol Gen Genet. 2000, 263:423-432.
    95. Krubasik P and Sandmann G. Molecular evolution of lycopene cyclase involved in the formation of carotenoids with ionone end groups. Biochem Soc Trans. 2000, 28:806-810.
    96. Krubasik P, Sandmann G. Molecular evolution of lycopene cyclases involved in the formation of carotenoids with ionone end groups. Biochemical Society Transactions. 2000, 28:806-810.
    97. Kumar S, Tamura K, Jakobsen IB. MEGA2: Molecular evolutionary genetics analysis software. Bioinformatics. 2001, 17:1244-1245.
    98. Kurkela S, and Franck M.Cloning and characterization of a cold- and ABA-inducible Arabidopsis gene. Plant Mol Biol. 1990, 15:137-144.
    99. Lee SH and Min DB. Effects, quenching mechanisms and kinetics of carotenoids in chlorophyll-sensitised photo-oxidation of soybean oil. J Agric Food Chem. 1990, 38(8):1630-1634.
    100. Lescot M, Déhais P, Moreau Y, et al. PlantCARE: a database of plant cis-acting regulatory elements and a portal to tools for in silico analysis of promoter sequences. Nucleic Acids Res. 2002, 30(1):325-327.
    101. Liang CW, Zhao FQ, Meng CX et al. Molecular cloning, characterization and evolutionary analysis of phytoene desaturase (PDS) gene from Haematococcus pluvialis. World Journal of Microbiology and Biotechnology. 2006, 22:59-64.
    102. Liang CW, Zhao FQ, Qin S et al. Molecular Cloning and Characterization of Phytoene Synthase Gene from a Unicellular Green Alga Haematococcus pluvialis. Progress in Biochemistry and Biophysics. 2006, 33(9):854-860.
    103. Liang CW, Zhao FQ, Wei W, Zhang XW, Qin S. Carotenoid Biosynthesis in Cyanobacteria: Structural and Evolutionary Scenarios Based on Comparative Genomics. International of Biological Science. 2006, 2:197-207.
    104. Liebler DC. Antioxidant reactions of carotenoids. Ann N Y Acad Sci. 1993, 691:20-31.
    105. Linden H, Misawa N, Saito T, Sandmann G. A novel carotenoid biosynthesis gene coding for ζ-carotene desaturase: functional expression, sequence and phylogenetic origin. Plant Mol Biol. 1994, 24:369-379.
    106. Linden H. Carotenoid hydroxylase from Haematococcus pluvialis: cDNA sequence, regulation and functional complementation. Biochim. Biophys. Acta 1999, 1446(3):203-212.
    107. Lokstein HC, Steglich WR, et al. Light-harvesting antenna function of phycoerythrin in Prochlorococcus marinus. Biochim Biophys Acta. 1999, 1410:97-98.
    108. Lotan T and Hirschberg J. Cloning and expression in Escherichia coli of the ketocarotenoid canthaxanthin in Haematococcus pluvialis. FEBS Lett. 1995, 364(2):125-128.
    109. Maresca JA, Frigaard NF, Bryant DA. Identification of a novel class of lycopene cyclases in photosynthetic bacteria. In Photosynthesis: Fundamental Aspects to Global Perspectives. Edited by van der Est A. and Bruce D, in press. Allen Press, 2005 Canada.
    110. Marquardt J, Lutz B, Wans S, et al. The gene family coding for the light-harvesting polypeptides of Photosystem I of the red alga Galdieria sulphuraria. Photosyn Res. 2001, 68:121-130.
    111. Mary I and Vaulot D. Two-component systems in Prochlorococcus MED4: Genomic analysis and differential expression under stress. FEMS Microbiol. Lett. 2003, 226:135-144.
    112. Matveyev AV, Young KT, Meng A and Elhai J. DNA methyltransferases of the cyanobacterium Anabaena PCC7120. Nucleic Acids Res. 2001, 29:1491-1506.
    113. Mayer MP, Nievelstein V, Beyer P. Purification and characterisation of a NADPH-dependent oxidoreductase from chloroplasts of Narcissus pseudonarcissus-a redox mediator possibly involved in carotene desaturation. Plant Physiol and Biochem. 1992, 30:389-398.
    114. Mazón G, Lucena J M and Campoy S. LexA-binding sequences in Gram-positive and cyanobacteria are closely related. Mol Ge. Genomics. 2004, 271(1):40-49.
    115. Mazouni K, Domain F and Chauvat F. Expression and regulation of the crucialplant-like ferredoxin of cyanobacteria. Mol Microbiol. 2003, 49(4):1019-1029.
    116. Meng CX, Liang CW, Su ZL, et al. There are two 5’flanking region of bkt encoding beta-carotene ketolase in Haematococcus pluvialias.Phycologia. 2006, 45(2):218-224.
    117. Meng CX, Wei W, Su ZL, Qin S. Characterization of carotenoid hydroxylase gene promoter in Haematococcus pluvialis. Indian J Biochem Biophys. 2006, 43(5):284-288.
    118. Miki W. Biological functions and activities of animal carotenoids. Pure Appl Chem. 1991, 63:141-146.
    119. Millar AJ, Kay SA. Integration of circadian and phototransduction pathways in the network controlling CAB gene transcription in Arabidopsis. Proc Natl Acad Sci, USA. 1996, 93:15491-15496.
    120. Misawa N, Satomi Y, Kondo K, Yam AY, Kajiwara S, Saito T, Ohtani T, Miki W. Structure and functional analysis of a marine bacterial carotenoid biosynthesis gene cluster and astaxanthin biosynthetic pathway proposed at the gene level. J Bacteriol. 1995, 177:6575-6584.
    121. Mochimaru M, Masukawa H, Takaichi S. The cyanobacterium Anabaena sp. PCC 7120 has two distinct β-carotene ketolases: CrtO for echinenone and CrtW for ketomyxol synthesis. FEBS Letters. 2005, 579:6111-6114.
    122. Muto Y, Moriwaki H. Antitumor activity of vitamin A and its derivatives. J. Natl Cancer Inst. 1984, 73(6):1389-1393.
    123. Niyogi KK. Photoprotection revisited. Annu Rev Plant Physiol. Plant Mol Biol. 1999, 50: 391-417.
    124. Nordin K, Heino P and Palva ET. Separate signal pathways regulate the expression of a low-temperature-induced gene in Arabidopsis thaliana (L.) Heynh. Plant Mol Biol. 1991, 16:1061-1072.
    125. Ohme-Takagi M, and Shinshi H. Structure and expression of a tobacco ?-1,3-glucanase gene. Plant Mol Biol. 1990, 15:941-946.
    126. Okada K, Saito T, Nakagawa T, Kawamukai M, Kamiya Y. Five Geranylgeranyl Diphosphate synthases expressed in different organs are localized into three subcellularcompartments in Arabidopsis. Plant Physiol. 2000, 122:1045-1050.
    127. Olson JA, Krinsky NI. The colorful, fascinating world of the carotenoids: important physiologic modulators. FASEB J. 1995, 9:1547-1550.
    128. Omelchenko MV, Makarova KS, Wolf YI, Rogozin IB, Koonin EV. Evolution of mosaic operons by horizontal gene transfer and gene displacement in situ. Genome Biol. 2003, 4:R55.
    129. Oscar H, et al. Photoprotective functions of carotenoids. In: Carotenoids: Chemistry and Biology. Krinsky N I, et al., Plenum Press, New York. 1990, pp: 229-236.
    130. Palmiter RD, Sandgren EP, et al. Heterologous introns can enhance expression of transgenes in mice. Proc Natl Acad Sci. 1991, 88:478-482.
    131. Palozza P and Krinsky NL. Astaxanthin and canthaxanthin are potent antioxidants in a membrane model. Arch Biochem Biophys. 1992, 297(2):291-295.
    132. Phadwal K. Carotenoid biosynthetic pathway: molecular phylogenies and evolutionary behavior of crt genes in eubacteria. Gene. 2005, 345:35-43.
    133. Qin S, Zhao F, Tseng CK. Evidence for positive selection in phycoerythrin genes of red algae and cyanobacteria Prochlorococcus and Synechococcus. Photosynthetica. 2005, 43:141-146.
    134. Richaud C and Zabulon G. The heme oxygenase gene (pbsA) in the red alga Rhodella violacea is discontinuous and transcriptionally activated during iron limitation. Proc Natl Acad Sci, USA. 1997, 94:11736-11741.
    135. Riechmann JL and Meyerowitz EM. The AP2/EREBP family of plant transcription factors. Biol Chem. 1998, 379:633-646.
    136. Rocap G, Distel DL, Waterbury JB and Chisholm SW. Resolution of Prochlorococcus and Synechococcus ecotypes by using 16S-23S ribosomal DNA internal transcribed spacer sequences. Appl Environ Microbiol. 2002, 68(3):1180-1191.
    137. Ronen G, Carmel-Goren L, Zamir D, Hirschberg J. An alternative pathway to β-carotene formation in plant chromoplast discovered by map-based cloning of beta and old-gold color mutations in tomato. Proc Nati Acad Sci USA. 2000, 97: 11102-11107.
    138. Ruban AV, Yong AJ, Pascal AA, Horton P. The effect of illumination on the蓝藻与绿藻类胡萝卜素合成基因的比较基因组学研究及代谢调控研究 梁成伟 Xanthophyll composition of the photosystem II light harvesting complexes of spinach thylakoid membranes. Plant Physiol.1994, 104:227-234.
    139. Saitou N, Nei M. The neighbor-joining method: a new method for reconstructing phylogenetic trees. J Mol Evol. 1987, 4: 406-425.
    140. Sandmann G. Genetic manipulation of carotenoid biosynthesis: strategies, problems and achievements. Trends Plant Sci. 2001, 6(1):14-17.
    141. Sandmann G. Molecular evolution of carotenoid biosynthesis from bacteria to plants. Physiol Plant. 2002, 116: 431-572.
    142. Sandmann G. Phytoene desaturases: genes, enzymes and phylogenetic aspects. J Plant Physiol .1994, 143:444-447.
    143. Schopf JW. Microfossils of the early Archean apex chert: new evidence of the antiquity of life. Science. 1993, 260:640-646.
    144. Schultz J, Milpetz F, Bork P, Ponting CP. SMART, a simple modular architecture research tool: Identification of signaling domains. Proc Natl Acad Sci, USA. 1998, 95:5857-5864.
    145. Sedkova N, Tao L, Rouvière PE, Cheng Q. Diversity of carotenoid synthesis gene clusters from environmental Enterobacteriaceae strains. Appl Environ Microb. 2005, 17:8141-8146.
    146. Shen Q, Zhang P, Ho THD. Modular nature of abscisic Acid (ABA) response complexes: composite promoter units that are necessary and sufficient for ABA induction of gene expression in barley. Plant Cell. 1996, 8:1107-1119.
    147. Shen QJ, Casaretto JA, Zhang P, et al. Functional definition of ABA-response complexes: the promoter units necessary and sufficient for ABA induction of gene expression in barley (Hordeum vulgare L.). Plant Mol Biol. 2004, 54(1):111-24.
    148. Shen QX, and Ho T-HD. Functional Dissection of an Abscisic Acid (ABA)-lnducible Gene Reveals Two lndependent ABA-Responsive Complexes Each Containing a G-Box and a Nove1 cis-Acting Element. The Plant Cell. 1995, 7:295-307.
    149. Simpson SD, Nakashima K, Narusaka Y, et al. Two different novel cis-acting elements of erd1, a clpA homologous Arabidopsis gene function in induction by dehydration stress and dark-induced senescence. Plant J. 2003, 33(2):259-270.
    150. Sonnhammer E. Eddy S, Birney E, Bateman A, Durbin R. Pfam: multiple sequence alignments and HMM-profiles of protein domains. Nucleic Acids Research.1998, 26(1):320-322.
    151. Steglich C, Mullineaux CW, Teuchner K, Hess WR, Lokstein H. Photophysical properties of Prochlorococcus marinus SS120 divinyl chlorophylls and phycoerythrin in vitro and in vivo. FEBS Lett. 2003b, 553:79-84.
    152. Steglich C, Psot AF, Hess WR. Analysis of natural populations of Prochlorococcus spp. in the northern Red Sea using phycoerythrin gene sequence. Environ Microbiol. 2003a, 5:681-690.
    153. Steiger S, Jackisch Y, Sandmann G. Carotenoid biosynthesis in Maresca Gloeobacter violaceus PCC7421 involves a single crtI-type phytoene desaturase instead of typical cyanobacterial enzymes. Arch Microbiol. 2005, 184:207-214.
    154. Steiger S, Sandmann G. Cloning of two carotenoid ketolase genes from Nostoc punctiforme for the heterologous production of canthaxanthin and astaxanthin. Biotech Lett. 2004, 26:813-817.
    155. Steinbrenner J and Linden H. Regulation of two carotenoid biosynthesis genes coding for phytoene synthase and carotenoid hydroxylase during stress-induce astaxanthin formation in the alga Haematococcus pluvialis. Plant Physiol. 2001, 125(2):810-817.
    156. Stickforth P, Steiger S, Hess WR, Sandmann G. A novel type of lycopene epsilon-cyclase in the marine cyanobacterium Prochlorococcus mainus MED4. Arch Microbiol. 2003, 179:409-415.
    157. Stock JB, Robinson VL and Goudreau PN. Two-component signal transduction. Annu Rev Biochem. 2000, 69:183-215.
    158. Stockinger EJ, Gilmour SJ and Thomashow MF. Arabidopsis thaliana CBF1 encodes an AP2 domain–containing transcriptional activator that binds to the C-repeat/DRE, a cis-acting DNA regulatory element that stimulates transcription in response to low temperature and water deficit. Proc Natl Acad Sci, USA. 1997, 94:1035-1040.
    159. Sujak A and Gruszecki WI. Organization of mixed monomolecular layers formed eith xanthyophyll pigments lutein or zeaxanthin and dipalmitoylphosphatidylcholine at the argon-water interface. Journal of Photochemistry and Photobiology B: Biology. 2000,59:42-47.
    160. Sujak A, Mazurek P and Gruszecki WI. Xanthophyll pigment lutein and zeaxanthin in lipid multibilayers formed with dimyristoylphosphatidylcholine. Journal of Photochemistry and Photobiology B: Biology. 2002, 68:39-44.
    161. Sujak A, Okulski W and Gruszecki WI. Organization of xanthyophyll pigments lutein and zeaxanthin in lipid membranes formed with dipalmitoylphosphatidylcholine. Biochemica et Biophysica Acta. 2000, 1509:255-263.
    162. Sun Z, Cunningham FX, Gantt E. Differential expression of two isopentenyl pyrophosphate isomerases and enhanced carotenoid accumulation in a unicellular chlorophyte. Proc Natl Acad Sci, USA. 1998, 95:11482-11488.
    163. Sun ZR, Gantt E, Cunningham Jr FX. Cloning and functional analysis of the β-carotene hydroxylase of Arabidopsis thaliana. J Biol Chem. 1996, 271:24349-24352.
    164. Susan Y, Fujimoto, Masaru Ohta, et al. Arabidopsis ethylene-responsive element binding factors act as transcriptional activators or repressors of GCC Box–mediated gene expression. Plant cell. 2000, 12:393-404.
    165. Takaichi S, Maoka T, Masamoto K. Myxoxanthophyll in Synechocystis sp PCC 6803 is Myxol 2’-Dimethyl-Fucoside, (3R,2’S)-Myxol 2’-(2,4-di-O-Methyl-α-L-Fucoside), not rhamnoside. Plant Cell Physiol. 2001, 42:756-762.
    166. Takaichi S, Mochimaru M, Maoka T, Katoh H. Myxol and 4-ketomyxol 2’-fucosides, not rhamnosides, from Anabaena sp. PCC 7120 and Nostoc punctiforme PCC 73102, and proposal for the biosynthetic pathway of carotenoids. Plant Cell Physiol. 2005, 46:497-504.
    167. Tanaka T, Morishita Y, et al. Chemoprevention of mouse urinary bladder by the naturally occurring carotenoid astaxanthin. Carcinogenesis. 1994, 15(1):15-19.
    168. Tao L, Picataggio S, Rouviere PE and Cheng Q. Asymmetrically acting lycopene bata-cylase (CrtLm) from non-photosynthetic bacteria. Mol Genet Genomics. 2004, 271:180-188.
    169. Teng CY, Qin S, Liu JG, et al. Transient Expression of lacZ in Bombarded Unicellular Green Alga Haematococcus pluvialis. J Applied Phycol. 2002, 14(6):497-500.
    170. Teramoto M, Takaichi S, Inomata Y, Ikenaga H and Misawa N. Structural and functional analysis of a lycopene beta-monocylase gene isolated from a unique marine bacterium that produces myxol. Febs Lett. 2003, 545:120-126.
    171. Thompson JD, Gibson TJ, Plewniak F, Jeanmougin F, Higgins DG. The CLUSTAL_X windows interface: exible strategies for multiple sequence alignment aided by quality analysis tools. Nucleic Acids Res. 1997, 25:4876-4882.
    172. Tietz A, Ruttkowski V, et al., Further investigations on the occurrence and the effects of abscisic acid in algae. Biochem Physiol Pflanzen. 1989, 184:259-266.
    173. Ting SC, Rocap G, King J and Chisholm SW. Phycobiliprotein genes of the marine photosynthetic prokaryote Prochlorococcus: evidence for rapid evolution of genetic heterogeneity. Microbiol. 2001, 147:3171-3182.
    174. Torrissen OJ and Christiansen R. Requirements for carotenoids in fish diets. J Appl Ichthyol. 1995, 11:225-230.
    175. Urao T, Yamaguchi-shinozaki K, Urao S, et al. An Arabidopsis myb homolog is induced by dehydration stress and its gene product binds to the conserved MYB recognition sequence. Plant Cell. 1993, 5(11):1529-1539.
    176. Velayos A, Blasco JL et al. Blue-light regulation of phytoene dehydrogenase (carB) gene expression in Mucor circinelloides. Planta. 2000, 210:938-946.
    177. Velayos A, Papp T, et al. Expression of the carG gene, encoding geranylgeranyl pyrophosphate synthase, is up-regulated by blue light in Mucor circinelloides. Curr Genet. 2003, 43:112-120.
    178. Verdoes JC, Krubasik P, Sandmann G and Ooyen van AJJ. Isolation and functional characterization of a novel type of carotenoid biosynthetic gene from Xanthophyllomyces dendrohous. Mol Gen Genet. 1999, 262:453-461.
    179. Villand P, Eriksson M, Samuelsson G. Carbon dioxide and light regulation of promoters controlling the expression of mitochondrial carbonic anhydrase in Chlamydomonas reinhardtii.Biochem J. 1997, 327:51-57.
    180. Vishnevetsky M and Ovadis M. Molecular mechanisms underlying carotenogenesis in the chromoplast: multilevel regulation of carotenoid-associated genes. Plant J. 1999, 20(4): 423-431.
    181. Viveiros M, Krubasik P, Sandmann G, Houssaini-Iraqui M. Structural and functionalanalysis of the gene cluster encoding carotenoid biosynthesis in Mycobacterium aurum A+. FEMS Microbiol Lett. 2000, 187: 95-101.
    182. Viveirosa M, Krubasik P, Sandmann G, Houssaini-Iraquic M. Structural and functional analysis of the gene cluster encoding carotenoid biosynthesis in Mycobacterium aurum A+.FEMS Microbiol Lett. 2000, 187:95-101.
    183. Wei W, Liang CW, Song Qin. Functional analysis of the promoter of bkt encoding beta-carotene ketolase in Haematococcus pluvialis, (in press)
    184. Willows RD, Mayer SM, Foulk MS, DeLong A, Hanson K, Chory J and Beale SI Phytobilin biosynthesis: The Synechocystis sp. PCC 6803 heme oxygenase-encoding ho1 gene complements a phytochrome-deficient Arabidopsis thaliana hy1 mutant. Plant Mol Biol. 2000, 113-120.
    185. Wilson GG and Murray NE. Restriction and modification systems. Annu Rev Genet. 1991, 25:585-627.
    186. Yamaguchi-Shinozaki K, Shinozaki K.A Novel cis-acting element in an Arabidopsis gene is involved in responsiveness to drought, low temperature, or high-salt stress. Plant Cell. 1994, 6(2): 251-264.
    187. Yan B, Raben N, et al., Identification and characterization of a tissue-specific silencer element in the first intron of the human acid maltase gene. Hum Genet. 2001, 109 (2):186-90.
    188. Yoshihara T, Washida H, Takaiwa F. A 45-bp proximal region containing AACA and GCN4 motif is suffiecient to confer endosperm-specific expression of the rice storage protein glutelin gene, GluA-3. FEBS Letters. 1996,383:213-218.
    189. Yutaka M, Keiji K, Toshiko S et al. Production of the carotenoids lycopene, β-carotene, and astaxanthin in the food yeast Candida utilis. Appl Environ Microbiol.1998, 64:1226-1229.
    190. Zhang X, Zhao F, Qin S. Cloning, expression and characterization of phycoerythrin gene from Ceramium boydenn. DNA Seq. 2006 (in press)
    191. Zhao F, Qin S. Comparative molecular population genetics of phycoerythrin locus in Prochlorococcus. Genetica. 2006b (in press)
    192. Zhao F, Qin S. Evolutionary analysis of phycobiliproteins: Implications for their structural and functional relationships. J Mol Evol. 2006a. (in press)
    193. Zhao F, Zhang XW, Liang CW, et al. Genome wide analysis of restriction- modification system in unicellular and filamentous cyanobacteria. Physiol Genomics. 2006, 24: 181-190.
    194. Ziegler RG, A review of epidemiologic evidence that carotenoids reduce the risk of cancer. J Nutr.1989, 119:116-122.
    195. 胡鸿均.中国淡水藻类[M].上海:上海科学技术出版社,1980
    196. 惠伯棣.类胡萝卜素化学及生物化学[M].北京:中国轻工业出版社.2004.
    197. 孟春晓. 雨生红球藻中虾青素合成关键酶基因的顺式作用元件研究. 2005, 中国科学院海洋研究所博士论文.
    198. 秦松,于道展,姜鹏,滕长英,曾呈奎.β-半乳糖苷酶基因(lacZ)在大型海藻裙带菜中的表达.高技术通讯, 200,13(7):87-89.
    199. 秦松,曾呈奎. 藻类基因工程. 海洋生物技术新进展.范晓,张士璀, 秦松,严小军,编著.北京:海洋出版社. 1999, pp.58-81.
    200. 滕长英,梁成伟,秦松,曾呈奎。雨生红球藻(Haematococcus pluvialis)基因工程选择试剂的筛选,海洋与湖沼,2005,36(4):302-306.
    201. 滕长英. 雨生红球藻控制虾青素合成的关键酶基因的转录调控元件. 2003, 中国科学院海洋研究所博士论文.
    202. 魏炜. 雨生红球藻中虾青素合成相关酶基因的转录调控序列分析. 2006, 中国科学院海洋研究所硕士论文.
    203. 吴乃虎. 基因工程原理第二版(下册). 北京:科学出版社,2001, 482-505.
    204. 谢先之,吴乃虎. 高等植物的内含子. 科学通报,2002, 47(10):731-737.
    205. 阎隆飞, 张玉麟. 分子生物学. Q7 / 3710, 北京农业大学出版社, 1997.
    206. 赵方庆. 螺旋藻基因组结构分析和藻胆蛋白的适应性进化. 2006, 中国科学院海洋研究所硕士论文.
    207. 庄惠如,卢海声等. 雨生红球藻(Haematococcus pluvialis Flotow)在胁迫条件下积累虾青素过程的超微结构研究. 电子显微学报, 2000, 19(2):137-142.

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