水生生物对微囊藻毒素去毒分子机理及调控因子研究
ADVANCE IN STUDIES ON MOLECULAR MECHANISMAND REGULATORY FACTORS OF MICROCYSTIN DETOXICATION IN AQUATIC ORGANISM
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摘要: 近年来,随着工农业的不断发展,排入水体的各种污染物不断增加,加速了淡水水域的富营养化进程,使得浮游藻类大量繁殖,有害藻类水华频繁发生,世界各地不断有藻类污染水体引起人畜患病甚至死亡的事件报道。在淡水藻类中,毒性最强、污染范围最广的为蓝藻门,目前确定的有毒藻种包括铜绿微囊藻(Microcystisaeruginosa)、水华鱼腥藻(An-abaenaflos-aguae)、水华束丝藻(Aphanizomenon flos-aquae)、阿氏颤藻(Oscillatoria agardii)、红色颤藻(Oscillato riarubescens)、泡沫节球藻(Nodularia spumigena)等。这些藻类所产生的毒素根据其致毒作用不同可分为三类:多肽肝毒素、生物碱类神经毒素及脂多糖内毒素[1],其中肝毒素的出现最为广泛且具有强促癌作用。肝毒素主要由铜绿微囊藻、水华鱼腥藻产生的微囊藻毒素(Microcystin,MC)和泡沫节球藻产生的节球藻毒素(Nodularin,NODLN)组成。淡水系统中,微囊藻毒素是肝毒素中危害最为严重的一类。有资料表明,饮用水中来自淡水系统的微囊藻毒素污染,很可能是除肝炎病毒和黄曲霉毒素以外导致肝癌的第三个重要原因[2]。自然水体中的微囊藻毒素已越来越多地影响到人类的饮用水安全。针对这一问题,目前采用的多是通过物理化学方法进行处理,虽然可以达到较好的效果,但其缺陷是成本太高。因此,研究水生生物对微囊藻毒素的去毒分子机理及相关调控因子,用生态学方法解决微囊藻毒素对自然水体的污染问题意义重大。
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Keywords:
- Microcystin /
- Detoxication /
- Glutathione S-Transferase (GST) /
- Conjugation /
- Regulatory Factors
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[1] Tang Z Y, YuY Q. Primary Liver Cancer [M]. Shanghai: Scientificand Technical Press. 1989, 30-37 [汤钊猷, 余业勤. 原发性肝癌. 上海: 科学技术出版社. 1989, 30-37]
[2] Sivonen K, Niemela S I, Lpist o L, et al. Toxic cyanobact erial bluegreenalgae in finish fresh and canstal waters [J]. Hydrobiologia,1990, 190: 267-275
[3] Hu Z Q, Liu Y D. Accumulation of microcystin-RR in Synechococcuselongatus and its toxic effects [J]. China Environmental Science,2005, 25(1): 23-27 [胡智泉, 刘永定. 微囊藻毒素在细长聚球藻中的积累及其毒性效应. 中国环境科学, 2005, 25 (1):23-27]5 期于 燕等: 水生生物对微囊藻毒素去毒分子机理及调控因子研究 741
[4] Pires L M, Karlsson K M, Meriluoto J A, et al. Assimilat ion anddepuration of microcystin-LR by the zebra mussel, Dreissena polymorpha[J]. Aquatic Toxicology, 2004, 69: 385-396
[5] He J Y, He Z R, Guo Q L. The toxicity of microcyst is aeruginosa tof ishes and daphnia [J]. Journal of Lake Science, 1997, 9(1): 49-56 [何家菀, 何振荣, 郭琼林. 有毒铜绿微囊藻对鱼和的毒性. 湖泊科学, 1997, 9(1): 49-56]
[6] Liu J K, Xie P. Direct control of microcystis bloom through the use ofPlanktivorous Carp- closure experiments and lake fishery pract ice [J].Ecol ogic Science, 2003, 22(3): 193-196 [刘建康, 谢平. 用鲢鳙直接控制微囊藻水华的围隔试验和湖泊实践. 生态科学,2003, 22(3): 193-196]
[7] Xie P, Liu JK. Pract ical success of biomanipulation using f ilter-feedingfish to control cyanobact eria blooms: a synthesis of decades of researchand applicat ion in a subtropical hypereut rophic lake [J]. Scientific World Journal, 2001, 1: 337-356
[8] Datta S, Jana B B. Control of bloom in a tropical lake: grazing eff-iciency of some herbivorous fishes [J]. Fish Biol, 1998, 53 (1):12-24
[9] Pflugmacher S, Wiegand C, Oberemm A, et al. Ident ifiation of anenzymat ically formed glutathione conjugat e of the cyanobacterial hepatotoxinmicrocystin-LR: the fist step of detoxication [J]. BiochimBiophys Acta, 1998, 1425(3): 527-533
[10] Beatt ie K A, Ressler J, Wiegand C, et al. Comparative eff ects andmetabolism of two microcystins and nodularin in the brine shrimpArtemia salina [J]. Aquatic Toxicology, 2003, 62: 219-226
[11] Best J H, Pflugmacher S, Wiegand C, et al. Effects of enteric bacterialand cyanobacterial lipopolysaccharides, and of microcystin-LR,on glut athione S-transferase activities in zebra fish (Danio rerio-[J].Aquat Toxicol, 2002, 60(3-4): 223-231
[12] Gehringer M M, Shephard E G, Downing T G, et al. An investigationinto the detoxifi cation of microcystin-LR by the glutathione pathwayin Balb/ c mice [J]. Int J Biochem Cell Biol, 2004, 36(5):931-941
[13] Gehringer M M, Downs K S, Downing T G, et al. An investigat ioninto the eff ect of selenium supplementation on microcyst in hepatotoxicity[J]. Toxicon, 2003, 41(4): 451-458
[14] Pinho G L, da Rosa C M, Maciel F E, et al. Antioxidant responsesaft er microcystin exposure in gills of an estuarine crab species pretreatedw ith vitamin E [J]. Ecotoxicology and Environmental Saf ety,2005, 61(3): 361-365
[15] Liang X F, Lin X T, Huang F, et al. The liver uncoupling prot ein 2gene of the red sea bream (Pagrus maj or-with reference to its phys-iological funct ion [J]. Acta Zoologica Sinica, 2003, 49 (1): 110)117 [梁旭方, 林小涛, 黄芬, 等. 真鲷肝脏解偶联蛋白2 (UCP2)基因及其功能的探讨. 动物学报, 2003, 49(1): 110-117]
[16] Liang X F, Ogat a H Y, Oku H, et al. Abundant and constant expressionof uncoupling protein 2 in the liver of red sea bream Pagrusmajor [J]. Comparative Biochemi stry and Physiol ogy Part A, 2003,136(3): 655-661
[17] Shephard G S, Stockenstrom S, Villiers D, et al. Photocatalyticdegradation of cyanobacterial microcystin toxins in water [J]. Toxicon,1998, 36(12): 1895-1901
[18] Shephard G S, Stockenstrom S, de Villiers D, et al. Degradation ofmicrocyst in toxins in a fall ing film photocat alytic reactor with immob-ilized t it anium dioxide catalyst [J]. Wat. Res, 2002, 36: 140-146
[19] Takenaka S, Watanabe M F. Microcyst in LR degradation by Pseudomonasaeruginosa alkaline protease [J]. Chemosphere, 1997, 34(4): 749-757
[20] Park H D, Sasaki Y, Maruyama T, et al. Degradation of thecyanobacterial hepatotoxin microcyst in by a new bact erium isolat edfrom a hypert rophic lake [J]. Environ Toxicol, 2001, 16(4): 337)343
[21] Yan H, Pan G, Zhang M M. Advances in the study of microcyst iontoxin [J]. Acta Ecologica Sinica, 2002, 22(11): 1968-1975 [闫海, 潘纲, 张明明, 等. 微囊藻毒素研究进展. 生态学报,2002, 22(11): 1968-1975]
[22] Bourne D G, Jones G J, Blakeley R L, et al. Enzymatic pathway forthe bacterial degradation of the cyanobacterial cyclic peptide toxin m-icrocystin LR [J]. Appl Environ Microbi ol, 1996, 62 (11): 4086)4094
[23] Brourne D G, Riddles P, Jones G J, et al. Characterization of a genecluster involved in bact erial degradation of the cyanobact erial t oxin m-icrocystin LR [J]. Environ Toxi col, 2001, 16(6): 523-534
[24] Saito T, Okano K, Park HD, et al. Detection and sequencing of themicrocyst in LR- degrading gene, mlrA, from new bacteria isolat edfrom Japanese lakes [J]. FEMS Microbi ol Lett, 2003, 229 (2):271-276
[25] Lu X W, Inamori Y H, Ding G J. Degradat ion of Microcystis viridisand microcyst ins with biological react ors [J]. China EnvironmentalScience, 1999, 9(2): 138-140 [吕锡武, 稻森悠平, 丁国际. 有毒蓝藻及藻毒素生物降解的初步研究. 中国环境科学, 1999, 9(2): 138-140]
[26] AO H Y, Shen Y W, Qiu C Q, et al. Biodetoxificat ionof algalpowerof toxic cyanobact eria from Dianchi lake [J]. Resources andEnvironment in the Yangtze Basin Jan, 2002, 1(1): 43-46 [熬鸿毅, 沈银武, 丘昌强, 等. 滇池水华蓝藻干粉制剂的生物脱毒实验. 长江流域资源与环境, 2002, 1(1): 43-46]
[27] Choi S H, Kim S G. Lipopolysaccharide inhibition of rat hepatic m-icrosomal epoxide hydrolase and glutathione S-transferase gene expressionirrespective of nuclear factor-kappaB activation [J]. BiochemPharmacol, 1998, 56(11): 1427-1436
[28] Best JH, Eddy F B, Codd G A. Effect s of Microcystis cells, cell extractsand lipopolysaccharide on drinking and l iver function in rainbowtrout Oncorhynchus mykiss Walbaum [J]. Aquat Toxicol, 2003, 64(4): 419-426
[29] Rushmore T H, Pickett C B. Glut athione S-transferases, structure,regulation, and therapeutic implicat ions [J]. J Biol Chem, 1993,268(16): 11475-11478
[30] Rushmore T H, King R G, Paulson K E, et al. Regulation of glutathioneS-transferase Ya subunit gene expression: identificat ion of aunique xenobiot ic-responsive element controlling inducible expressionby planar aromatic compounds [J]. Proc Natl Acad Sci USA, 1990,87(10): 3826-3830-2 水 生 生 物 学 报31卷
[31] Paulson K E, Darnell J E Jr, Rushmore T, et al. Analysis of the upstreamelements of the xenobiotic compound-inducible and positionallyregulated glutathione S-transf erase Ya gene [J]. Mol Cell Biol,1990, 10(5): 1841-1852
[32] Denison M S, Fisher JM, andWhit lock J P Jr. Protein-DNA interactionsat recognit ion sit es for the dioxin-Ah receptor complex [J]. JBiol Chem, 1989, 264(28): 16478-16482
[33] Fujisawa-Sehara A, Yamane M, Fuji-i Kuriyama Y. A DNA-bindingfactor specific for xenobioti c responsive element s of P-450c gene existsas a cryptic form in cytoplasm: its possible translocation to nucleus[J]. ProcNatl Acad Sci USA, 1988, 85(16): 5859-5863
[34] Denison M S, Fisher J M, Whit lock J P Jr. Inducible, receptor-dependentprotein-DNA interactions at a dioxin-responsive transcriptionalenhancer [J]. Proc Natl Acad Sci USA, 1988, 85(8): 2528-2532
[35] Neuhold L A, Shirayoshi Y, Ozato K. Regulation of mouse CYP1A1gene expression by dioxin: requirement of two cis- acting element s duringinduction [J]. Mol Cell Biol, 1989, 9(6): 2378-2386
[36] Whit lock J P Jr. The regulation of gene expression by 2, 3, 7, 8-tetrachlorodibenzo-p-dioxin [J]. Pharmacol Rev, 1987, 39(2): 147)161
[37] Rushmore T H, Picket t C B. Transcript ional regulat ion of the rat glutathioneS-transferase Ya subunit gene. Characterizat ion of a xenobiotic-responsive element controlling inducible expression by phenolic antioxidants[J]. J Biol Chem, 1990, 265(24): 14648-14653
[38] Rushmore T H, Morton M R, Pickett C B. The antioxidant responsiveelement. Act ivation by oxidat ive stress and identificat ion of the DNAconsensus sequence required for functional act ivity [J]. J Biol Chem,1991, 266(18): 11632-11639
[39] Rozen F, Nguyen T, Pickett C B. Isolation and characterization of ahuman glutathione S-transferase Ha1 subunit gene [J]. Arch BiochemBi ophys, 1992, 292: 589-593
[40] Rohrdanz E, Nguyen T, Pickett C B. Isolation and characterization ofthe human glutathione S-transferase A2 subunit gene [J]. ArchBiochem Biophys, 1992, 298: 667-677
[41] Klone A, Hussnatt er R, Seis H. Cloning, sequencing and charact er-ization of the human alpha glut athione S-transferase gene correspondingto the cDNA clone pGTH2 [J]. Biochem J, 1992, 285: 925-928
[42] Leaver M J, George S G. Three repeated glutathione s-transf erasegenes from a marine fish, the Plaice (Pleuronectes platessa-[J].Marine Environmental Research, 1996, 42(1-4): 19-23
[43] Leaver M J, George S G. St ructure of the plaice glutathione s-transferasea gene [J]. Marine Environmental Research, 1995, 39 (1)4): 33-37
[44] reshwater fishes [J]. EcologicScienc, 2005, 24(2): 6-8 [廖婉琴, 梁旭方, 王琳, 等. 淡水鱼类微囊藻毒素去毒酶基因的克隆. 生态科学, 2005, 24 (2):6-. Liao W Q, Liang X F, Wang L, et al. Cloning of the microcystindetoxifizymegene in the main Chinese freshwater fishes [J]. EcologicScienc, 2005, 24(2): 6-8 [廖婉琴, 梁旭方, 王琳, 等. 淡水鱼类微囊藻毒素去毒酶基因的克隆. 生态科学, 2005, 24 (2):6-8]
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