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1.
贵阳花溪区石灰土林地土壤重金属含量特征及其污染评价   总被引:23,自引:1,他引:22  
选取贵阳市花溪区典型石灰土林地土壤作为研究对象,分析了林地石灰岩和土壤中7种重金属(Cu、Zn、Mn、Cd、Ni、Pb、Co)的含量特征,以贵州省土壤背景值和全国石灰(岩)土类背景值为评价标准进行林地土壤重金属污染评价和潜在生态风险评价.结果表明:林地石灰岩以Pb的平均含量(40.21mg·kg-1)最高,Zn的(5.78 mg·kg-1)最低,7种重金属平均含量高低顺序为:Pb>Ni>Mn>Co>Cu>Cd>Zn;林地土壤中以Mn的平均含量(451.16 mg·kg-1以上)最高,Cd的(2.87mg·kg-1以下)最低,7种重金属含量的变异系数在8.57%~63.10%之间,Zn的平均含量明显低于贵州省土壤背景值和全国石灰(岩)土类背景值,Cu、Mn、Cd、Pb、Ni、Co的平均含量高于或接近于贵州省土壤背景值和全国石灰(岩)土类背景值.Cu、Zn、Mn、Ni、Co,Ni与Pb,Cd与Pb,Cd与Co来源相同的可能性较大,而Cd与Cu、Ni,Pb与Mn、Cu、Co的来源不同;石灰土偏碱性,富含Ca、Mg元素,有利于重金属Cd、Pb的累积.单因子污染指数和多因子综合指数(内梅罗指数法)与Hakanson潜在生态危害指数的评价结果一致,林地土壤重金属综合污染指数在3.67以上,达到重污染程度,以Cd的污染指数(4.94以上)最高,污染程度最为严重,其次是Pb(1.82以上),Zn、Mn污染程度最低,林地土壤重金属潜在生态危害指数(RI)为173.75以上,为中度生态危害程度,产生最大生态危害的是Cd,其次是Pb、Ni、Co、Cu,危害程度最小的是Mn、Zn,在相同的成土母岩和人为活动影响下,无林地土壤重金属的综合污染指数和潜在生态危害指数均明显高于有林地.  相似文献   

2.
临安市雷竹林土壤重金属污染特征及生态风险评价   总被引:13,自引:0,他引:13  
为了解临安市雷竹林土壤重金属污染特征,采集并测定了160个土壤样品的Hg、As、Cu、Pb、Zn、Cd、Cr、Ni、Co、Mn等重金属含量,采用单因子污染指数和内梅罗综合污染指数对雷竹林土壤重金属污染程度进行分析,并应用Hankanson潜在生态风险指数法对雷竹林土壤重金属潜在生态风险进行评价.结果表明:雷竹林土壤重金属Hg、As、Cu、Pb、Zn、Cd、Cr、Ni、Co、Mn的平均含量分别为0.16、7.41、34.36、87.98、103.98、0.26、59.12、29.56、11.44、350.26mg·kg-1,Pb、Cd、Zn和Cu平均值超过浙江省土壤背景值,分别是对应背景值的2.89、1.70、1.12、1.12倍.经单因子污染指数评价,不同重金属元素的平均污染程度大小依次为Pb>Cd>Cu=Zn>Hg>As>Ni>Co>Cr>Mn,其中Pb有中度污染,Cd、Cu和Zn有轻度污染.经内梅罗综合污染指数评价,160个样点都受到不同程度的重金属污染,轻度污染、中度污染和重度污染水平所占比率分别为55.6%、29.4%和15.0%.各重金属单因子潜在生态风险指数平均值评价结果显示,只有Cd污染达到中等生态风险,其他重金属均为轻微生态风险,而局部采样点Cd和Hg单因子潜在生态风险指数最大值分别达到256.82和187.33,存在很强生态风险.重金属综合因子潜在生态风险指数评价结果表明,临安市雷竹林土壤整体上存在轻微生态风险.  相似文献   

3.
6种重金属对赤子爱胜蚓的急性毒性效应与风险评价   总被引:3,自引:0,他引:3       下载免费PDF全文
【背景】近年来,土壤重金属污染问题日益凸显,对生态环境、食品安全和人体健康构成了严重威胁,其急性毒性尚未明确。【方法】采用滤纸接触法和人工土壤法测定了铜(Cu2+)、锌(Zn2+)、镍(Ni+)、镉(Cd2+)、铅(Pb2+)和锰(Mn2+)等6种重金属对赤子爱胜蚓的急性毒性效应,并参照欧盟指令91/414/EEC标准评价了其环境风险。【结果】滤纸接触法48h测定结果表明,6种重金属对蚯蚓的LC50为3.17(2.53~3.81)~90.42(69.45~140.47)μg.cm-2,其毒性次序为Cu2+>Zn2+>Ni+>Cd2+>Pb2+>Mn2+。人工土壤法14d测定结果表明,6种重金属对蚯蚓的LC50为1347(1236~1453)~6936(6144~8930)mg.kg-1,其毒性次序为Cu2+>Cd2+>Ni+>Zn2+>Mn2+>Pb2+。风险评价结果显示,Cu2+、Zn2+、Ni+、Cd2+、Pb2+和Mn2+等6种重金属的暴露比(toxicity/exposureratio,TER)分别为3.37、4.46、8.68、1428、13.87和5.85。【结论与意义】6种重金属对土壤动物蚯蚓均具有潜在的毒性效应。Cu2+、Zn2+、Ni+、Mn2+等4种重金属对赤子爱胜蚓存在急性毒性风险,而Cd2+和Pb2+对赤子爱胜蚓的急性毒性风险水平是可接受的。该评价结果可为我国制定基于风险的土壤环境质量标准提供依据。  相似文献   

4.
为探索刺楸对受污染土壤重金属的富集和修复效应, 以南京栖霞山的乡土树种刺楸及其根际周边土壤为研究对象, 截取其根基部年轮盘及根际土壤样本, 采用ICP-AES法测定年轮及土壤样本中重金属(Cu、Cd、Cr、Mn、Ni、Pb、Zn)元素含量。结果表明: 栖霞山样地中的土壤受Mn、Pb和Zn污染最为严重, 存在Cu、Cd、Mn、Pb、Zn元素的高度复合污染, Cd、Cr、Cu、Ni、Zn在土壤和年轮中存在相关性, Mn和Pb则没有表现出明显的相关性; 刺楸修复受Cd、Mn、Pb、Zn污染的土壤效果并不显著, 更适用于Cr、Cu、Ni污染的土壤修复; 鉴于Cu元素含量变化特征, 刺楸也可以作为反映当地污染历史的记录载体; 刺楸年轮中的重金属元素之间存在交互作用, 其中Cd与Zn元素含量高度相关(r=0.984, p<0.01), 在刺楸年轮吸收重金属元素的过程中, Cu与Cd、Cr、Mn、Zn元素具有协同作用, Mn元素对其他元素有一定的拮抗作用。  相似文献   

5.
通过模拟基于干旱区绿洲土壤Cd-Pb-Zn-Ni复合污染下的油菜盆栽试验,采用Tessier五步连续浸提法探究了重金属复合污染对油菜生长的影响及其各形态的转化归趋和生物有效性.结果显示,随着Cd-Pb-Zn-Ni复合胁迫水平的升高,油菜的干重先增加后减小,根系的生长由促进作用转变为抑制作用;对照土壤中4种重金属元素均以残渣态为主要赋存形态,可交换态的含量均很小;随着外源重金属的添加,油菜种植土壤中4种重金属元素的各形态含量随之增加,Cd、Pb、Zn的可交换态和Ni的碳酸盐结合态对外界胁迫响应强度最大,Cd、Pb、Zn、Ni的活性增加,且Cd、Pb的主要赋存形态迅速转变为碳酸盐结合态和铁锰氧化态,Zn的主要赋存形态由残渣态和碳酸盐结合态过渡到碳酸盐结合态和铁锰氧化态,Ni的主要赋存形态为碳酸盐结合态;Cd、Zn在茎叶中的含量大于根系,Pb、Ni反之,油菜能将Cd、Zn更多的运输至茎叶,Pb、Ni则主要积累在根系;油菜茎叶吸收Cd和油菜各部位吸收Zn的主要贡献形态为可交换态,根吸收Cd的主要贡献形态由可交换态转变为有机结合态,根吸收Pb和油菜各部位吸收Ni的主要贡献形态为碳酸盐结合态.  相似文献   

6.
哈尔滨市不同类型人工林土壤重金属含量   总被引:2,自引:0,他引:2  
Sun HZ  Lu XJ  Chen MY  Cai CJ  Zhu N 《应用生态学报》2011,22(3):614-620
以东北林业大学城市林业示范研究基地9种人工林(兴安落叶松林、樟子松林、黑皮油松林、黄波罗林、胡桃楸林、水曲柳林、白桦林、蒙古栎林和针阔混交人工林)为对象,分析林地土壤不同层次(0~10 cm和10-30 cm)A8、Cd、Cu、Ni、Pb、Zn 6种重金属含量,并以哈尔滨市土壤背景值为标准,采用综合污染指数法评价各林型土壤重金属污染状况.结果表明:不同类型人工林同一土层重金属含量差异显著;除了As和Ni,同一人工林土壤重金属含量均随土壤深度增加呈下降趋势.各类型人工林同一土层重金属含量以Zn最高(62.29~126.35mg·kg-1),Cd最低(0.06~0.47 mg·kg-1).6种重金属含量由高到低顺序为:Zn>Pb>Cu(Ni)>Ni(Cu)>As>Cd,累积程度为:Cd>Pb>Zn>Cu>Ni>As.林地土壤Pb、Cd、Cu、Zn间(除水曲柳林)及其与土壤有机质、N、P、K(除水曲柳林和蒙古栎林)显著相关,且以上4种重金属含量高于背景值,为人为输入;Ni和As含量与本地背景值相当,为自然因素,不同林型土壤内梅罗综合污染指数依次为:水曲柳林>黄波罗林>针阔混交林>胡桃楸林>樟子松林>黑皮油松林>兴安落叶松林>白桦林>蒙古栎林.  相似文献   

7.
为了了解不同土壤重金属浓度梯度及污染梯度下香樟不同器官的富集特征,测定了香樟树叶、树枝、树干和根际土壤中6种重金属元素(Cu、Zn、Pb、Cr、Mn、Ni)的含量.结果表明: 香樟地上部分重金属含量因器官、元素种类、根际土壤重金属浓度的不同而存在差异.香樟树叶和树枝重金属含量的大小顺序均为:Mn>Zn>Cu>Cr>Pb>Ni,树干重金属含量为:Mn>Zn>Cr>Pb>Ni>Cu.树叶对Mn的富集系数较高,为2.409;树干对Ni的富集系数较高,分别为树叶、树枝的8.6和17倍,且在不同土壤重金属浓度梯度下,香樟树干对Cu、Zn、Pb、Cr、Ni的富集系数均明显高于其他器官.香樟地上部分器官对Cu、Zn、Pb、Cr、Mn、Ni 6种重金属元素的综合富集能力大小顺序为:树叶>树干>树枝.随着土壤重金属污染等级的增加,香樟地上部分各器官的富集系数均逐渐降低.研究区域平均胸径为22 cm的单株香樟对重金属元素富集效能的大小顺序为:树叶>树干>树枝,其中树干对Cu、Zn、Pb、Cr、Ni的积累量均显著高于树叶和树枝.表明香樟对6种重金属元素均有一定的富集能力,并且树干对Pb和Ni的富集效能明显,分别占地上部分总积累量的82.7%和91.9%,能很好地富集并稳固土壤中的Pb和Ni,可作为修复治理土壤重金属污染的备选树种.  相似文献   

8.
为研究交通运输造成的重金属污染特征及潜在生态风险,选取兰州市某交通干道,利用原子吸收分光光度计检测了金属元素的含量,并利用单因子指数法和潜在生态风险指数法评价了土壤污染程度和潜在生态风险,进而分析了土壤重金属污染对绿化植物叶绿素和Ca含量的影响。结果表明: 城市交通导致土壤重金属Cr、Mn、Zn、Cu和Ni的含量均显著增高,且Cr、Pb和Cu达到了中度污染,潜在生态风险排序为Cu>Pb>Cr>Ni>Zn>Mn;槐树、月季、紫叶李和冬青卫矛对交通源重金属Pb、Mn、Zn、Ni等表现出不同程度的积聚作用;落叶植物槐树、月季和紫叶李叶片中叶绿素含量表现为路侧采样点>对照点,而常绿植物冬青卫矛和侧柏的叶绿素含量为对照点>路侧采样点,所有绿化植物叶片中Ca含量表现为路侧采样点>对照点,高的叶绿素和Ca含量可能有利于绿化植物在土壤重金属污染环境中生存。交通运输导致研究区域土壤中重金属Cr、Mn、Zn、Cu和Ni等的积累;槐树、月季、紫叶李和冬青卫矛等对Pb、Mn、Zn和Ni具有不同程度的积聚作用,可推荐为相应重金属污染土壤绿化植物。  相似文献   

9.
马国芳  王江  张崇邦 《微生物学报》2008,35(6):0882-0887
本文研究了Pb、Zn、Cu和Cd对3种蛋白酶产生菌:碱性地衣芽孢杆菌2709(Bacillus licheniformis 2709)、中性枯草杆菌1.398(Bacillus subtilis1.398)和酸性宇佐美曲霉537(Aspergillus usamii 537)生长及其酶活性的影响, 并采用生长抑制皿分析(GIPA)方法针对3种菌株在Pb、Zn、Cu、Cd不同胁迫浓度下的生长量进行打分, 分析其耐性与抗性指标(MTC与MIC)。结果表明4种重金属在超过一定临界浓度后, 对3种菌株的生长和蛋白酶活性均产生了较大的抑制作用。碱性蛋白酶对4种重金属均具有较大的适应性, 其次是中性蛋白酶对Zn和Cd具有一定的适应性, 而酸性蛋白酶对4种重金属均表现出被抑制状态。3种菌株对Pb和Zn耐性与抗性最高(2.0 mmol/L~6.0 mmol/L), 其次是对Cd也具有一定的抗性(0.5 mmol/L~0.75 mmol/L)。  相似文献   

10.
分析了3种重金属离子(Cd2+、Cu2+、Zn2+)对向日葵种子胚根伸长和早期幼苗生长的影响.结果表明,3种重金属离子对向日葵胚根伸长的抑制作用依次为:Cd2+>Cu2+>Zn2+.3种重金属胁迫明显降低了幼苗生长和叶绿素含量,并显著提高了H2O2水平.其中Cd2+胁迫引起幼苗H2O2爆发高于Cu2+和Zn2+胁迫.进一步分析植株抗氧化系统的变化发现,随着重金属离子浓度的增加,向日葵幼苗酶类抗氧化物质SOD和CAT的活性表现为先增加后降低的趋势;重金属胁迫提高了非酶类的抗氧化物质脯氨酸和GSH的含量.其中Cd2+和Zn2+胁迫对脯氨酸含量变化的影响大于Cu2+胁迫;而Cu2+胁迫对GSH含量变化的影响大于Cd2+和Zn2+胁迫.  相似文献   

11.
重金属胁迫条件下空心莲子草的生长和营养特征分析   总被引:1,自引:0,他引:1  
空心莲子草是一种常见的水生植物,并能在重金属污染的水体或附近土壤中生长.本研究发现,空心莲子草能富集6种常见的重金属元素,其富集能力为:Zn2+>Mn2+>Pb2+>Cu2+>Cd2+>Cr3+.高浓度(1 mmol/L) Cu2+、Mn2+、Zn2+和Cr3+ 等重金属胁迫处理条件下,空心莲子草的根冠比增加,生物干重、总根长和总根表面积都相应降低.此外,高浓度(1 mmol/L) Pb2+、Cd2+、Cu2+或Zn2+分别胁迫处理条件下,空心莲子草的K+、Ca+和Mg+等元素的含量变化差异显著(P<0.05).以上研究表明,空心莲子草通过改变体内钾钙镁等重要生长元素营养情况来适应重金属污染的胁迫,有很强的富集重金属元素的能力,进而降低污染、净化水体.空心莲子草对重金属污染的生长响应及体内重要矿物元素营养特性之间的相互关系,可能为重金属污染的水土生物修复提供理论依据.  相似文献   

12.
A differential effect is found of various bivalent cations (Ba2+, Ca2+, Mg2+, Cd2+, Co2+, Mn2+, Ni2+, Zn2+ and Hg2+) on stability of intermolecular Py-Pu-Pu triplex with different sequence of base triads. Ca2+, Mg2+, Cd2+, Co2+, Mn2+, Ni2+ and Zn2+ do stabilize the d(C)n d(G)n d(G)n triplex whereas Ba2+ and Hg2+ do not. Ba2+, Ca2+, Mg2+ and Hg2+ destabilize the d(TC)n d(GA)n d(AG)n triplex whereas Cd2+, Co2+, Mn2+, Ni2+ and Zn2+ stabilize it. The complexes we observe are rather stable because they do not dissociate during time of gel electrophoresis in the co-migration experiments. Chemical probing experiments with dimethyl sulfate as a probe indicate that an arbitrary homopurine-homopyrimidine sequence forms triplex with corresponding purine oligonucleotide in the presence of Mn2+ or Zn2+, but not Mg2+. In the complex the purine oligonucleotide has antiparallel orientation with respect to the purine strand of the duplex. Specifically, we have shown the formation of the Py-Pu-Pu triplex in a fragment of human papilloma virus HPV-16 in the presence of Mn2+.  相似文献   

13.
1. The inflow of Mn2+ across the plasma membranes of isolated hepatocytes was monitored by measuring the quenching of the fluorescence of intracellular quin2, by atomic absorption spectroscopy and by the uptake of 54Mn2+. The inflow of other divalent metal ions was measured using quin2. 2. Under ionic conditions which resembled those present in the cytoplasmic space, Mn2+, Zn2+, Co2+, Ni2+ and Cd2+ each quenched the fluorescence of a solution of Ca2(+)-quin2. 3. The addition of Mn2+, Zn2+, Co2+, Ni2+ or Cd2+ to cells loaded with quin2 caused a time-dependent decrease in the fluorescence of intracellular quin2. Plots of the rate of decrease in fluorescence as a function of the concentration of Mn2+ reached a plateau at 100 microM-Mn2+. 4. The rate of decrease in fluorescence induced by Mn2+ was stimulated by 20% in the presence of vasopressin. The effect of vasopressin was completely inhibited by 200 microM-verapamil. Adrenaline, angiotensin II and glucagon also stimulated the rate of decrease in the fluorescence of intracellular quin2 induced by Mn2+. 5. The rate of decrease in fluorescence induced by Zn2+, Co2+, Ni2+ or Cd2+ was stimulated by between 20 and 190% in the presence of vasopressin or angiotensin II. 6. The rates of uptake of Mn2+ measured by atomic absorption spectroscopy or by using 54Mn2+ were inhibited by about 20% by 1.3 mM-Ca2+o and stimulated by 30% by vasopressin. 7. Plots of Mn2+ uptake, measured by atomic absorption spectroscopy or with 54Mn2+, as a function of the extracellular concentration of Mn2+ were biphasic over the range 0.05-1.0 mM added Mn2+ and did not reach a plateau at 1.0 mM-Mn2+. 8. It is concluded that (i) hepatocytes possess both a basal and a receptor-activated divalent cation inflow system, each of which has a broad specificity for metal ions, and (ii) the receptor-activated divalent cation inflow system is the receptor-operated Ca2+ channel.  相似文献   

14.
The three isozymes of 3-deoxy-D-arabino-heptulosonate-7-phosphate synthase from Escherichia coli were overproduced, purified, and characterized with respect to their requirement for metal cofactor. The isolated isozymes contained 0.2-0.3 mol of iron/mol of enzyme monomer, variable amounts of zinc, and traces of copper. Enzymatic activity of the native enzymes was stimulated 3-4-fold by the addition of Fe2+ ions to the reaction mixture and was eliminated by treatment of the enzymes with EDTA. The chelated enzymes were reactivated by a variety of divalent metal ions, including Ca2+, Cd2+, Co2+, Cu2+, Fe2+, Mn2+, Ni2+, and Zn2+. The specific activities of the reactivated enzymes varied widely with the different metals as follows: Mn2+ greater than Cd2+, Fe2+ greater than Co2+ greater than Ni2+, Cu2+, Zn2+ much greater than Ca2+. Steady state kinetic analysis of the Mn2+, Fe2+, Co2+, and Zn2+ forms of the phenylalanine-sensitive isozyme (DAHPS(Phe)) revealed that metal variation significantly affected the apparent affinity for the substrate, erythrose 4-phosphate, but not for the second substrate, phosphoenolpyruvate, or for the feedback inhibitor, L-phenylalanine. The tetrameric DAHPS(Phe) exhibited positive homotropic cooperativity with respect to erythrose 4-phosphate, phophoenolpyruvate, and phenylalanine in the presence of all metals tested.  相似文献   

15.
The effect of divalent cations on bovine sperm adenylate cyclase activity was studied. Mn2+, Co2+, Cd2+, Zn2+, Mg2+ and Ca2+ were found to satisfy the divalent cation requirement for catalysis of the bovine sperm adenylate cyclase. These divalent cations in excess of the amount necessary for the formation of the metal-ATP substrate complex were found to stimulate the enzyme activity to various degrees. The magnitude of stimulation at saturating concentrations of the divalent cations was strikingly greater with M2+ than with either Ca2+, Mg2+, Zn2+, Cd2+ or Co2+. The apparent Km was lowest for Zm2+ (0.1 - 0.2 mM) than for any of the other divalent cations tested (1.2 - 2.3 mM). The enzyme stimulation by Mn2+ was decreased by the simultaneous addition of Co2+, Cd2+, Ni2+ and particularly Zn2+ and Cu2+. The antagonism between Mn2+ and Cu2+ or Zn2+ appeared to have both competitive and non-competitive features. The inhibitory effect of Cu2+ on Mn2+-stimulated adenylate cyclase activity was prevented by 2,3-dimercaptopropanol, but not by dithiothreitol, L-ergothioneine, EDTA, EGTA or D-penicillamine. Ca2+ at concentrations of 1-5 mM was found to act synergistically with Mg2+, Zn2+, Co2+ and Mn2+ in stimulating sperm adenylate cyclase activity. The Ca2+ augmentation of the stimulatory effect of Zn2+, Co2+, Mg2+ and Mn2+ appeared to be specific.  相似文献   

16.
Biosorption of heavy metals such as Pb2+, Ni2+, Cd2+, Cu2+, Cr3+ and Zn2+ by petiolar felt-sheath of palm (PFP) from contaminated water was examined. PFP was found to efficiently remove all the toxic metal ions with selectivity order of Pb2+ > Cd2+ > Cu2+ > Zn2+ > Ni2+ > Cr3+. The uptake was rapid, with more than 70% completed within 15 min. The bound metal ions were successfully desorbed and the PFP fibrous-biomass remained effective after several adsorption-desorption cycles.  相似文献   

17.
Binding of 125I-[Nle15]gastrin to albumin purified from porcine serum, from porcine gastric mucosal cytosol, and from bovine serum has been demonstrated by covalent cross-linking and ultracentrifugation. Binding was enhanced in the presence of Zn2+, Ni2+, Cu2+, Co2+, and Cd2+, but not Ca2+, Mg2+, or Mn2+. The best fit to the binding data for bovine serum albumin was obtained with a model assuming two nonequivalent binding sites. The affinity of both sites for gastrin was increased in the presence of 100 microM Zn2+ or Ni2+ ions. The highest association constant observed was 2.3 X 10(5) M-1 in the presence of 100 microM Zn2+ ions. The similarity of the Zn(2+)-dependence of binding for bovine and porcine serum albumins, despite the replacement of His3 by Tyr, suggested that the N-terminal metal ion-binding site was not involved. Although all gastrin affinities were reduced by 50% in the presence of 150 mM NaCl, the Zn(2+)-dependence of binding was retained. We therefore propose that the ternary complex of gastrin, Zn2+ ions, and albumin may play a physiological role in the serum transport of Zn2+ ions and in the uptake of Zn2+ ions from the lumen of the gastrointestinal tract.  相似文献   

18.
Sun G  Budde RJ 《Biochemistry》1999,38(17):5659-5665
In addition to a magnesium ion needed to form the ATP-Mg complex, we have previously determined that at least one more free Mg2+ ion is essential for the activation of the protein tyrosine kinase, Csk [Sun, G., and Budde, R. J. A. (1997) Biochemistry 36, 2139-2146]. In this paper, we report that several divalent metal cations, such as Mn2+, Co2+, Ni2+, and Zn2+ bind to the second Mg2+-binding site of Csk with up to 13200-fold higher affinity than Mg2+. This finding enabled us to substitute the free Mg2+ at this site with Mn2+, Co2+, Ni2+, or Zn2+ while keeping ATP saturated with Mg2+ to study the role of the free metal cation in Csk catalysis. Substitution by these divalent metal cations resulted in varied levels of Csk activity, with Mn2+ even more effective than Mg2+. Co2+ and Ni2+ supports reduced levels of Csk activity compared to Mg2+. Zn2+ has the highest affinity for the second Mg2+-binding site of Csk at 0.65 microM, but supports no kinase activity, acting as a dead-end inhibitor. The inhibition by Zn2+ is reversible and competitive against free Mg2+, noncompetitive against ATP-Mg, and mixed against the phosphate accepting substrate, polyE4Y, significantly increasing the affinity for this substrate. Substitution of the free Mg2+ with Mn2+, Co2+, or Ni2+ also results in lower Km values for the peptide substrate. These results suggest that the divalent metal activator is an important element in determining the affinity between Csk and the phosphate-accepting substrate.  相似文献   

19.
Mn2+ and Zn2+ exhibit a striking ability to block the induction by Sn2+ and Ni2+ of haem oxygenase (EC 1.14.99.3) in kidney. The blocking effects of Mn2+ and Zn2+ were found to be greatest on simultaneous administration, time-dependent when administered up to 8 h before the inducing metal ions, and ineffective when administered as little as 10 min after the inducing metal ions. The decreases in cytochrome P-450 and haem contents and the sequential changes in delta-aminolaevulinate synthase (EC 2.3.1.37) activity that occur concomitant with haem oxygenase induction were largely eliminated with simultaneous or prior treatment with Mn2+ or Zn2+, but not when Mn2+ or Zn2+ was administered after Sn2+ or Ni2+. Mn2+ and Zn2+ did not increase the catabolism of the enzyme in vivo. Zn2+ on simultaneous administration was also able substantially to block the induction of haem oxygenase by Co2+, Cd2+ and Ni2+ in liver. The Zn2+ blockade of Cd2+ induction was examined in detail, and prior or simultaneous administration of Zn2+ was found to be effective in blocking the induction of haem oxygenase and the concomitant decreases in cytochrome P-450 and haem contents, ethylmorphine demethylase activity and the sequential changes in delta-aminolaevulinate synthase activity. Zn2+ administration 10 min or more after Cd2+ was ineffective in preventing the occurrence of these perturbations in haem metabolism. These findings describe a new and striking biological property of Mn2+ and Zn2+, and indicate the existence of significant metal ion interactions in the control of haem metabolism.  相似文献   

20.
Two Zn-finger proteins, TFIIIA (a constituent of 7S RNP particles) and p43 (a constituent of 42S RNP particles), were detected in ovary extracts of juvenile Xenopus laevis females by in vitro binding of radiolabeled divalent metals. Proteins fractionated by SDS-PAGE (sodium dodecylsulfate-polyacrylamide gel electrophoresis) were transferred by Western blotting onto nitrocellulose membranes, probed with 65Zn2+, 63Ni2+, or 109Cd2+, and visualized by autoradiography. Detection limits for TFIIIA were approx 0.07 micrograms/well by 109Cd(2+)-probing, 0.13 micrograms/well by 65Zn(2+)-probing, and 0.26 mu/well by 63Ni(2+)-probing. Protein p43 was more clearly visualized by probing with 63Ni2+ than with 65Zn2+ or 109Cd2+. After purified TFIIIA was cleaved with cyanogen bromide, 65Zn2+, 109Cd2+, and 63Ni2+ distinctly labeled the 22 kDa middle fragment; 65Zn2+ and 109Cd2+ also labeled the 11 kDa N-terminal fragment, but did not label the 13 kDa C-terminal fragment. These results are consistent with the notion that the radioligands were bound to finger-loop domains of TFIIIA, which occur in the middle and N-terminal fragments. Based on the abilities of nonradioactive metal ions to compete with 65Zn2+ for binding to TFIIIA on Western blots, the relative affinities of the metals for TFIIIA were ranked as follows: Zn2+ = Cu2+ greater than or equal to Hg2+ greater than Cd2+ greater than Co2+ greater than or equal to Ni2+. Even at a 1000-fold molar excess, Mn2+ did not compete with 65Zn2+ for binding to TFIIIA. Probing Western blots with the radiolabeled metal ions greatly facilitates the detection, isolation, and quantitation of TFIIIA and p43.  相似文献   

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