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NaCl浓度对杜氏盐藻中1种NAD^+依赖的3-磷酸甘油脱氢酶基因表达的影响 被引量:1

Effects of salinities on gene expression of a(NAD+)-dependent glycerol-3-phosphate dehydrogenase in Dunaliella salina
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摘要 考察NaCl浓度变化对杜氏盐藻细胞形态和单细胞甘油含量变化的影响,并应用实时定量PCR技术检测NaCl浓度变化对杜氏盐藻3-磷酸甘油脱氢酶同工酶中1种NAD+依赖的3-磷酸甘油脱氢酶基因表达的影响。结果表明:不同浓度NaCl长期培养时杜氏盐藻细胞形态和体积的变化较小,但当NaCl浓度快速变化时细胞形态和体积变化显著。杜氏盐藻在不同浓度NaCl条件下长期培养,随着NaCl浓度增长,单细胞甘油含量不断积累,且杜氏盐藻能通过快速降低或提高单细胞甘油含量来应对低渗或高渗震动。不同浓度NaCl长期培养时,杜氏盐藻中3-磷酸甘油脱氢酶基因的表达水平与NaCl浓度呈显著负相关,但低渗或高渗震动处理2 h后,3-磷酸甘油脱氢酶基因的表达水平与NaCl浓度无显著性关系。 Effects of salinity changes on variation of cell shape and single cell glycerol content of Dunaliella salina were investigated and effects of salinity changes on the gene expressions of a(NAD+)-dependent G3pdh(EC1.1.1.8) among G3pdh isozymes in D.salina were detected by real-time quantitative PCR.Results showed that the changes of shape and volume of D.salina cell cultured chronically at various salinities were minor.When the salinity changed rapidly,the variations of cell shape and cell volume of D.salina were significant,which were recovered basically after 2 h except treated by high salinity.It was found that some lipid globules in the surface of D.salina cells when the salinity increased from 2.0 to 4.0-5.0 mol/L NaCl rapidly.When D.salina was cultured chronically at various salinities,the accumulation of single cell glycerol increased with increased salinity,and D.salina also could rapidly decrease or increase single cell glycerol contents to adapt to hypoosmotic or hyperosmotic shock.The expression level of G3pdh in D.salina grown at various salinities was significantly inversely correlated with the salinity.There was no significant correlation between the expression level of G3pdh and salinity after two hours of treatment by hyperosmotic or hypoosmotic shock.
出处 《华中农业大学学报》 CAS CSCD 北大核心 2013年第5期77-83,共7页 Journal of Huazhong Agricultural University
基金 广东省科技计划项目(2009B020307013)
关键词 杜氏盐藻 NaCl浓度 细胞形态 甘油含量 3-磷酸甘油脱氢酶 实时定量PCR Dunaliella salina concentrations of NaCl cell shape glycerol content glycerol-3-phosphate dehydrogenase real-time quantitative PCR
分类号 O943 [理学]
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参考文献14

  • 1张加强,潘凤英,廖小芳,周瑞阳,杨健,黄龙.红麻杂交种幼苗生长对盐胁迫的响应[J].华中农业大学学报,2011,30(5):552-557. 被引量:7
  • 2CHEN H, JIANG J G. Osmotic responses of Dunaliella to the changes of salinity:J]. J Cell Physiol,2009,219(2) = 251-258.
  • 3FRASER P D, BRAMLEY P M The biosynthesis and nutri* tional uses of carotenoids[J], Prog Lipid Res,2004,43(3) :228-265.
  • 4ALKAYAL F, ALBION R L,TILLETT R L,et al. Expressed sequence tag (EST) profiling in hyper saline shocked Du-naliella salina reveals high expression of protein synthetic apparatus components[J]. Plant Sci,2010,179(5) :437-449.
  • 5HE Q H,QIAO D R,BAI L H?et aL Cloning and characterization of a plastidic glycerol 3-phosphate dehydrogenase cDNA from Du-naliella salina [J]. J Plant Physiol, 2007,64(2) : 214-220.
  • 6GEE R, COYAL A? BYERRUM R U, et al. Two isoforms of dihydroxyacetone phosphate reductase from the chloroplasts of Dunaliella tertiolecta [J]. Plant Physiol, 1993,103 (1): 243-249.
  • 7CHEN H JIANG J G,WU G H. Effects of salinity changes on the growth of Dunaliella salina and the isozyme activities of glycerol-3-phosphate dehydrogenase [J3. J Agric Food Chem, 2009,57(14):6178-6182.
  • 8CUI L Q,CHAI Y R,LI J,et al. Identification of a glucose-6-phosphate isomerase involved in adaptation to salt stress of Dunaliella salina [J]. J Appl Phycol, 2010,22(5) : 563-568.
  • 9PICK U. Adaptation of the halotolerant alga Dunaliella to high salinity[G]//LAUCHI A,LUTTGE U. Salinity: environ-ment, plants, molecules. Dordrecht: Klewer Academic Publishers,2002:97-112.
  • 10PINONTOAN R, YU AS A T, ANDERCA M I,et al. Cloning of a cDNA encoding a 66-kDa Ca2+ -dependent protein kinase (CDPK) from Dunaliella tertiolecta (Chlorophyta)[J]. J Phy-col,2000,36(3):545-552.

二级参考文献43

  • 1黄益群,焦新之.二羟丙酮还原酶在杜氏盐藻渗透调节过程中的特性[J].植物生理学报(0257-4829),1993,19(3):250-256. 被引量:6
  • 2李红萍,焦新之.杜氏盐藻渗透调节过程中的甘油代谢途径[J].植物生理学报(0257-4829),1994,20(1):91-99. 被引量:20
  • 3弋良朋,马健,李彦.盐胁迫对3种荒漠盐生植物苗期根系特征及活力的影响[J].中国科学(D辑),2006,36(A02):86-94. 被引量:45
  • 4李宗贤 侯兆芳 韦应碧等.杂交高粱的胚根优势及在种子工作中的利用.山西农业科学,1983,:16-17.
  • 5YAO Y,NI Z, ZHANG Y, et al. Identification of differentially expressed genes in leaf and root between wheat hybrid and its parental inbreds using PCR-based eDNA subtraetion[J]. Plant Molecular Biology, 2005,58(3): 367-384.
  • 6李琳 焦新之.应用蛋白染色剂考马斯亮蓝G-250测定蛋白质的方法.植物生理学通讯,1980,(6):52-55.
  • 7Akhtar,N.,Blomberg,A.,and Adler,L.(1997).Osmoregulation and protein expression in a pbs2 △mutant of Saccharomyces cerevisiae during adaptation to hypersaline stress.FEBS Lett.403,173-180.
  • 8Avron,M.(1992).Osmoregulation In Dunaliella:Physiology,Biochemistry and Biotechnology,M.Avron,and A.Ben-Amotz,eds (Florida:CRC Press),pp.135-164.
  • 9Belmans,D.,and van Laere,A.(1987).Glycerol enzymes and inter-mediates during adaptation of Dunaliella tertiolecta cells to hyper-osmotic stress.Plant Cell Environ.10,185-190.
  • 10Ben-Amotz,A.,and Avron,M.(1973).The role of glycerol in the osmotic regulation of the halophilic alga Dunaliella parva.Plant Physiol.41,875-878.

共引文献30

同被引文献37

  • 1李红萍,焦新之.杜氏盐藻渗透调节过程中的甘油代谢途径[J].植物生理学报(0257-4829),1994,20(1):91-99. 被引量:20
  • 2陈琴,张福,姜润林.3种营养物质对极端嗜盐绿色杜氏藻生长的影响[J].苏盐科技,2006(4):21-23. 被引量:2
  • 3Zhang N, Wang F, Meng X, Luo S, Li Q, Dong H, Xu Z, Song R. Molecular cloning and characterization of a tre- halose-6-phosphate synthase/phosphatase from Dunaliel- la viridis. Mol Bio Rep, 2011, 38(4): 2241 2248.
  • 4Wang Z, Gerstein M, Snyder M. RNA-Scq: a revolutionary tool for transcriptomics. Nat Rev Genet, 2009, 10(1): 57-63.
  • 5Costa V, Angelini C, De Feis 1, Ciccodicola A. Uncovering the complexity of transcriptomes with RNA-Seq. J Bio- reed Biotechnol, 201 O, 2010: Article ID 853916.
  • 6Ozsolak F, Milos PM. RNA sequencing: advances, chal- lenges and opportunities. Nat Rev Genet, 2011, 12(2): 87-98.
  • 7Au KF, Jiang H, Lin L, Xing Y, Wong WH. Detection of splice junctions from paired-end RNA Seq data by Spli- ceMap. NuclAcids Res, 2010, 38(14): 4570-4578.
  • 8Sanger F, Nicklen S, Coulson AR. DNA sequencing with chain-terminating inhibitors. Proc Natl Acad Sci USA, 1977, 74(12): 5463 5467.
  • 9Margulies M, Egholm M, Altman WE, Attiya S, Bader JS,Bemben LA, Berka J, Braverman MS, Chen Y J, Chen ZT, Dewell SB, Du L, Fierro JM, Gomes XV, Godwin BC, He W, Helgesen S, Ho CH, Irzyk GP, Jando SC, Alenquer ML, Jarvie TP, Jirage KB, Kim JB, Knight JR, Lanza JR, Lea- mon JH, Lefkowitz SM, Lei M, Li J, Lohman KL, Lu H, Makhijani VB, McDade KE, McKenna MP, Myers EW, Nickerson E, Nobile JR, Plant R, Puc BP, Ronan MT, Roth GT, Sarkis GJ, Simons JF, Simpson JW, Srinivasan M, Tartaro KR, Tomasz A, Vogt KA, Volkmer GA, Wang SH, Weiner MP, Yu PG, Begley RF, Rothberg JM. Genome sequencing in microfabricated high-density picolitre reactors. Nature, 2005, 437(7057): 376-380.
  • 10Wilhelm BT, Marguerat S, Watt S, Schubert F, Wood V, Goodhead I, Penkett C J, Rogers J, Bihler J. Dynamic re- pertoire of a eukaryotic transcriptome surveyed at sin- gle-nucleotide resolution. Nature, 2008, 453(7199): 1239- 1243.

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