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作 者:周向红[1,2] 李信书[2] 阎斌伦[1] 易乐飞[1,2] 王萍[2]
机构地区:[1]淮海工学院江苏省海洋生物技术重点实验室,江苏连云港222005 [2]淮海工学院海洋学院,江苏连云港222005
出 处:《河南农业科学》2011年第10期111-114,共4页Journal of Henan Agricultural Sciences
基 金:江苏省海洋生物技术重点实验室开放课题(2008HS004);淮海工学院自然科学研究项目(2010150023)
摘 要:为了研究条斑紫菜的重金属解毒机制,分别采用Pb2+1、4、7、10 mg/L对条斑紫菜叶状体进行短期铅胁迫,同时,用10 mg/L的Pb2+对叶状体进行持续铅胁迫,胁迫处理后提取总RNA并采用实时荧光定量PCR技术检测条斑紫菜半胱氨酸合成酶基因(PyCSase-B)的表达变化。结果显示,铅胁迫能迅速且显著诱导PyCSase-B的表达。短期铅胁迫试验中,随着Pb2+质量浓度的升高,PyCSase-B的表达量呈先上升而后下降的趋势,在7 mg/L Pb2+胁迫下,PyCSase-B的表达量最高,是未处理样品的2.73倍。持续铅胁迫试验中,在前6 h内随着处理时间的增加,PyCSase-B的表达逐步上升,在6 h时PyCSase-B的表达量最高,是未处理样品的3.71倍;在8~12 h内PyCSase-B的表达量一直在较高水平波动。铅胁迫诱导PyCSase-B表达,说明PyCSase-B参与了条斑紫菜叶状体的重金属解毒过程。To investigate the mechanism of heavy metal detoxification in intertidal red alga Porphyra yezoensis Udea,the expression of cysteine synthase gene(PyCSase-B) in P.yezoensis thalli responding to lead stress was examined.Thalli were subjected to seawater treatment with different concentration of lead(1,4,7,10 mg/L Pb2+)for 2 h,and then subjected to seawater treatment with 10 mg/L Pb2+ for 12 h.Then total RNA was extracted from thalli,and the relative mRNA levels of PyCSase-B were examined using real-time fluorescence quantitative PCR.The result showed lead stress could rapidly and significantly induce the expression of PyCSase-B in P.yezoensis thalli.In the treatment of short-term lead stress,the expression of PyCSase-B was induced under 1 mg/L Pb2+ stress,reached its peak under 7 mg/L Pb2+ stress,and then fall.The relative mRNA level of PyCSase-B under 7 mg/L Pb2+ stress was 2.73-fold higher than untreated sample.In the treatment of continuous lead stress,during the first 6 h the expression of PyCSase-B increased gradually,and reached its peak at 6 h.The relative mRNA level of PyCSase-B at 6 h was 3.71-fold higher than untreated sample.From 8 h to 12 h,the expression of PyCSase-B fluctuated at a high level.
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