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1.
镉、汞复合污染对土壤脲酶和酸性磷酸酶活性的影响   总被引:13,自引:0,他引:13  
通过土壤培养试验, 研究了重金属镉(Cd)、汞(Hg)复合污染对小粉土和黄红壤脲酶和酸性磷酸酶活性的影响.结果表明:整个培养过程中,Cd、Hg单一及复合污染都对两种土壤中脲酶和酸性磷酸酶的活性具有明显抑制作用,且随重金属浓度增强而增强(浓度≤1 mg·kg-1Cd除外).与单一Cd或Hg污染相比,同剂量Cd和Hg复合污染时两种酶活性的净变化量均大于0,表明Cd和Hg复合污染在两种土壤中对土壤脲酶和酸性磷酸酶活性的抑制作用均表现为一定的协同作用.所有处理黄红壤脲酶和酸性磷酸酶活性均高于小粉土,这可能与黄红壤有机质和粘粒含量相对较高有关.  相似文献   

2.
1.氢醌对土壤脲酶活性的抑制率及其持续的时间同氢醌浓度成正相关,与土壤脲酶活性成负相关。2.氢醌能有效地抑制施入土壤中尿素氨的挥发,而对铵盐和尿素的硝化强度产生强烈抑制。3.在麦秸还田土壤中,由于脲酶活性增高而提高了施入尿素的水解速度,故需提高氢醌用量;但由于麦秸的“氮因子效应”又固定了尿素分解产物及其氧化产物,从而弥补了氢醌失效后可能造成氮素的继续损失。  相似文献   

3.
砷对土壤脲酶活性影响的研究   总被引:15,自引:4,他引:11  
采用模拟方法对As污染土壤脲酶特征进行了研究.结果表明,土壤中As浓度在0~200mg·kg^-1浓度范围内,反应初期脲酶活性变化无明显规律;一年后砷激活土壤脲酶活性,二者达到显著或极显著正相关.随As浓度增加,土壤脲酶Km值基本不变或略有增加,Vmax增大,从机制上揭示出As加速脲酶-尿素复合物的解离.厩肥和无肥土样脲酶对As的反应类似,只是变化幅度有所差异.  相似文献   

4.
施用缓/控释尿素对玉米苗期土壤生物学活性的影响   总被引:1,自引:0,他引:1  
采用盆栽试验,模拟田间生态环境,研究了施用不同种缓/控释氮素底肥对玉米苗期土壤硝酸还原酶、脲酶活性及微生物量碳、氮的影响.结果表明,施用硝化抑制剂(双氰胺)和脲酶抑制剂(n-丁基硫代磷酰三胺)涂层大颗粒尿素肥料的土壤硝酸还原酶活性最高;施用大颗粒尿素,脲酶活性最强,微生物量碳、氮最高.施用醋酸酯淀粉包膜大颗粒尿素、包膜双氰胺涂层大颗粒尿素、丙烯酸树脂包膜双氰胺涂层大颗粒尿素与不施氮肥土壤脲酶活性较高;每种处理微生物量碳与氮变化完全一致.施用醋酸酯淀粉包膜硝化和脲酶抑制剂涂层大颗粒尿素肥料,土壤微生物量碳、氮最低.同种膜材料包膜抑制剂涂层大颗粒尿素制成的缓/控释氮肥,对土壤生物学活性的影响效果好于直接包膜大颗粒尿素;丙烯酸树脂包膜大颗粒尿素制成的缓/控释氮肥,对氮素的控释效果明显好于醋酸酯淀粉包膜.  相似文献   

5.
通过土壤培养实验、紫外光谱和荧光光谱技术,研究了不同温度下Cd对土壤脲酶催化活性、动力学性质的影响及其机理。结果表明:(1)在供试温度范围内,土壤脲酶活性、动力学参数Vmax和Vmax/Km值与温度呈正相关,且土壤脲酶活性随着培养时间延长呈现先增后减的趋势; (2)土壤脲酶活性、动力学参数Vmax和Vmax/Km值与Cd^2+呈显著负相关,表明Cd对土壤脲酶的抑制作用为非竞争性抑制,且抑制程度随处理温度升高而加强; (3)低浓度Cd处理刀豆脲酶后,随着体系中Cd^2+的增加,脲酶的紫外吸收光谱发生红移,荧光发射峰发生蓝移。 关  相似文献   

6.
重金属污染区土壤酶活性变化   总被引:5,自引:1,他引:4  
王涵  高树芳  陈炎辉  王果 《应用生态学报》2009,20(12):3034-3042
从福建龙岩新罗区特钢厂污灌区农田采集土壤,测定土壤基本理化性质及脲酶、纤维素酶、碱性磷酸酶、多酚氧化酶、过氧化氢酶活性和Cu、Cd、Pb、Zn含量,探讨重金属污染和土壤性质对土壤酶活性的影响.结果表明: 4种全量或有效态重金属与土壤脲酶、纤维素酶、碱性磷酸酶和多酚氧化酶活性呈显著正相关,与过氧化氢酶活性呈显著或极显著负相关;土壤pH与碱性磷酸酶活性呈极显著正相关,粉粒含量与过氧化氢酶活性呈显著负相关.经通径分析,重金属污染刺激了脲酶、多酚氧化酶和纤维素酶活性,但对碱性磷酸酶活性的影响较小.有效态Cu、Cd、Pb、Zn对过氧化氢酶活性的直接影响并不大,但通过间接途径抑制了过氧化氢酶活性.土壤理化性质对5种土壤酶活性的影响较大,碱解氮直接抑制了脲酶活性;全磷直接刺激了碱性磷酸酶和过氧化氢酶活性,并通过有效磷刺激了纤维素酶活性;有效磷直接刺激了纤维素酶活性,直接抑制了碱性磷酸酶和过氧化氢酶活性;全钾直接抑制了碱性磷酸酶和多酚氧化酶活性;速效钾通过有效磷刺激了纤维素酶活性;土壤颗粒组成明显影响多酚氧化酶和过氧化氢酶活性.5种酶活性与土壤Cu、Cd、Pb、Zn含量之间的关系不明确,因此其活性不是指示土壤Cu、Cd、Pb、Zn污染的良好指标.  相似文献   

7.
镉污染对水稻土微生物量、酶活性及水稻生理指标的影响   总被引:35,自引:0,他引:35  
水稻盆栽条件下,研究了外源Cd不同处理对土壤微生物学指标、土壤酶活性及部分水稻生理指标的影响.结果表明,土壤微生物量C和N开始随Cd浓度增加而上升,到一定浓度时则随Cd浓度增加而下降,其转折点因土壤性质有所差异.同时土壤酶活性变化规律与土壤微生物量C、N变化规律相似,但其转折点浓度因土壤类型及土壤酶种类不同而有差异.Cd污染后的变异系数依次为:脱氢酶>酸性磷酸酶>脲酶.土壤呼吸作用强度和代谢熵都随Cd浓度增大而缓慢增加.水稻叶绿素含量随Cd处理浓度增加表现出先上升后下降,其转折点受供试土壤性质不同而不同;脯氨酸含量与过氧化物酶活性随着Cd处理浓度增大而增加.Cd污染后水稻生理指标的变异系数在黄松田水稻土中依次为过氧化物酶活性>叶绿素含量>脯氨酸含量;黄红壤性水稻土中依次为过氧化物酶活性>脯氨酸含量>叶绿素含量.相关分析表明,种植水稻条件下Cd污染对土壤微生物量、酶活性及水稻生理指标的影响是相辅相成的.  相似文献   

8.
外源硒对大豆产量、植株氮磷含量及土壤酶活性的影响   总被引:14,自引:2,他引:12  
利用盆栽试验,研究了不同浓度、不同价态外源se对大豆产量、N、P含量及与N、P代谢密切联系的土壤脲酶和磷酸酶活性的影响.结果表明,施用浓度为0.25和0.5μg·g^-1土的Se^4+和Se^6+后,大豆产量、含N量及土壤脲酶活性增加,大豆含P量和土壤磷酸酶活性降低.当Se^6+浓度为0.5μg·g^-1土时,大豆植株含N量与土壤脲酶活性呈极显著的抛物线相关关系;Se^6+浓度为0.25μg·g^-1土时,大豆植株含P量与土壤磷酸酶活性呈极显著的抛物线相关关系。Se^4+处理的大豆N、P含量和土壤脲酶和磷酸酶活性均无显著相关关系。  相似文献   

9.
与氮转化有关的土壤酶活性对抑制剂施用的响应   总被引:41,自引:6,他引:35  
利用室内模拟培养试验,研究好气条件下施用尿素后土壤脲酶、脲酸还原酶、亚硝酸还原酶和羟胺还原酶活性对脲酶抑制剂氢醌(HQ)与硝化抑制剂包被碳化钙(ECC)和双氰胺(DCD)组合(HQ ECC、HQ DCD)的响应、结果表明,HQ DCD组合与其它抑制剂处理相比能更有效地降低土壤脲酶活性,增加硝酸还原酶、亚硝酸还原酶、羟胺还原酶活性,不同处理土壤脲酶、亚硝酸还原酶和羟胺还原酶活性与土壤NH4^ 、NO3^-、NH3挥发和N2O排放速率间存在不同形式的显著相关关系:土壤脲酶、亚硝酸还原酶和羟胺还原酶活性之间存在不同形式的显著正相关关系。  相似文献   

10.
重金属Cd、Zn、Cu、Pb对土壤微生物和酶活性的影响   总被引:3,自引:0,他引:3  
采用室内培养实验(25℃),研究了不同培养时间下重金属Cd、Zn、Cu、Pb(浓度分别为50,800,400,800mg.kg-1)污染对土壤微生物和酶活性的影响。结果表明,土壤蔗糖酶、过氧化氢酶和脱氢酶活性随着培养时间的增加而显著下降,在培养20d的时候达到最小值,然后酶活性缓慢升高。Cu对脲酶活性以及Cd对酸性磷酸酶和脲酶活性的抑制作用随时间增加而增加。土壤微生物生物量碳、细菌、真菌和放线菌数量随培养时间的增加均表现出先降低后升高的变化趋势。Cd和Cu对微生物生物量氮的抑制作用则随着培养时间的增加而增强,在培养30d时微生物生物量氮到达最低值,分别较培养10天减少了12.6%和16.5%。  相似文献   

11.
Summary The concentration of nickel in some soils may be insufficient to meet the requirements of enzymes such as urease in soybeans and hydrogenase in Rhizobium. In an initial evaluation of nickel availability, several soils were examined for nickel content and microbial urease activity. Total and extractable nickel were determined by atomic emission spectrometry. Purified glucose and urea were added to soils to stimulate microbial growth and urease activity, the latter of which was monitored by the rate of decomposition of14C urea. Nickel also was added to some samples to determine if the indigenous supply was limiting. In one low-nickel soil (total Ni 13 ppm) urease activity increased 150% in response to additional nickel, while other soils (total Ni 22–3491 ppm) failed to respond to nickel. However, additional nickel did stimulate urease activity (up to 109%) in 3 out of 10 soils to which purified CaCO3 was added. Presumably the rise in pH associated with this treatment decreased nickel availability. Additions of Co, Mn, Fe, or Cu had no consistent effect on urease activity, thus indicating that the response to Ni was specific. Nickel fertilization increased leaf urease and nodule hydrogenase activity of soybeans grown in low-nickel soil, however, yield was not improved. These results may have practical implications in the nutrition of plants and micro-organisms that metabolize H2 and urea.  相似文献   

12.
Thallus samples of £. prunastri (L.) Adi, floated on 40 mM urea developed urease (EC 3.5.1.5.) activity which levelled off after 6h. L-Arguiine, L-ornitfaine and patrescine added to the incubation media intitially enhanced the effect of urea, but the urease activity ceased after 4h of incubation in the presence of the latter two compounds or when L-arginine was used; as the sole source of nitrogen. This decline in activity was observed after 6h when L-arginine was added to urea-containing media. The loss of urease activity is thought to result from the synthesis of repressers in the presence of the amino acids, whereas putrescine appears to affect membrane permeability by increasing the uptake of urea by the cells. Declining urease activity in the latter case would then be due to feedback inhibition caused by the excess of ammonia produced in both hydrolysis of urea and oxidation of putrescine.  相似文献   

13.
Dialysis Culture of T-Strain Mycoplasmas   总被引:8,自引:4,他引:4       下载免费PDF全文
Using dialyzing cultures of T-strain mycoplasmas, it was possible to make some observations relevant to the growth and metabolism of these organisms which would not be possible in nondialyzing cultures due to growth inhibition of the organisms by elevated pH and increased ammonium ion concentration in media containing urea. The rate of ammonia accumulation was found to be related to the initial urea concentration in the medium and could not be accounted for by any change in the multiplication rate of the organisms. More ammonia was generated than could be accounted for by the added urea alone, suggesting that an ammonia-producing activity other than urease may be present in T-strain mycoplasmas. Titers above 107 color change units per ml were achieved in dialysis cultures of a T-strain mycoplasma in the presence of urea, and such titers were maintained for approximately 60 h during dialysis culture in the absence of added urea.  相似文献   

14.
Occurrence of urease in T strains of Mycoplasma   总被引:23,自引:10,他引:13       下载免费PDF全文
A previously unknown metabolite necessary for growth of T strains of Mycoplasma in artificial culture media has been identified as urea. The source of this metabolite was the mammalian plasma or serum enrichment of the culture medium. Normal horse serum was the most satisfactory native protein enrichment for cultivation of T strains of mycoplasma, and it is believed that its superior performance in agar and fluid culture media is associated with its relatively high urea content (approximately 40 mg/100 ml). T-strain urease activity was maximal at pH 6.0 +/- 0.5. This is also the optimal pH for growth of T strains. Substrate concentrations greater than 1.0% urea were inhibitory to growth and urease activity of T-strain organisms, and optimal urea concentrations in fluid media appeared to lie within the range of 0.008 to 0.01 m. This range of urea concentration permitted maximal growth of T-strain organisms without rapid loss of viability due to excessive ammonia accumulation and rise in pH to lethal levels. T strains of Mycoplasma were cultivated in a serum-free fluid medium containing urea as the only added metabolite and nitrogen source. T strains are the only known human mycoplasmas which exhibit urease activity, and this biochemical marker can be employed as an aid in the detection and identification of T strains of Mycoplasma (urease color test) and in distinguishing T strains from other members of the human Mycoplasma group.  相似文献   

15.
The influence of urease activity on N distribution and losses after foliar urea application was investigated using wild-type and transgenic potato (Solanum tuberosum cv Désirée) plants in which urease activity was down-regulated. A good correlation between urease activity and (15)N urea metabolism (NH(3) accumulation) was found. The general accumulation of ammonium in leaves treated with urea indicated that urease activity is not rate limiting, at least initially, for the assimilation of urea N by the plant. It is surprising that there was no effect of urease activity on either N losses or (15)N distribution in the plants after foliar urea application. Experiments with wild-type plants in the field using foliar-applied (15)N urea demonstrated an initial rapid export of N from urea-treated leaves to the tubers within 48 h, followed by a more gradual redistribution during the subsequent days. Only 10% to 18% of urea N applied was lost (presumably because of NH(3) volatilization) in contrast to far greater losses reported in several other studies. The pattern of urease activity in the canopy was investigated during plant development. The activity per unit protein increased up to 10-fold with leaf and plant age, suggesting a correlation with increased N recycling in senescing tissues. Whereas several reports have claimed that plant urease is inducible by urea, no evidence for urease induction could be found in potato.  相似文献   

16.
【目的】棒酸(Clavulanic acid)是棒状链霉菌(Streptomyces clavuligerus)产生的β-内酰胺酶抑制剂,其合成过程中产生副产物脲,旨在探讨脲对棒酸合成的影响。【方法】通过发酵过程中脲和铵盐添加实验、阻断脲酶活性以及pH梯度实验研究脲对棒酸合成影响。【结果】脲添加实验结果表明:低浓度脲降低棒酸产量,当添加脲浓度达到20 mmol/L时,完全抑制棒酸合成。由于脲酶可以把脲水解为铵离子,导致铵离子浓度及pH提高,因此,通过阻断棒状链霉菌脲酶活性,可以更准确地反映脲对棒酸合成的影响。结果发现,脲酶敲除株发酵液中脲大量积累,浓度高达10 mmol/L,但棒酸产量没有明显降低,说明在该浓度下脲自身并不能抑制棒酸合成。添加脲降低野生菌棒酸产量,可能是脲被水解为铵离子或其引起的pH变化所致。而棒酸发酵液添加铵盐的结果显示铵离子对棒酸产量没有抑制作用;另外,pH梯度实验证实不同pH对棒酸产量影响较大。【结论】排除了脲和铵离子对棒酸合成的抑制作用,证实了脲酶水解脲导致pH提高是脲添加导致野生菌棒酸产量降低的真正原因,为进一步阐明棒酸合成调控机制提供了根据。  相似文献   

17.
The urea-hydrolyzing activity of a T-strain mycoplasma was studied in experiments using whole cells and cell-free enzyme preparations by measuring the release of 14CO2 from [14C]urea. Under the conditions used, the urea concentration optimum is approximately 5.6 X 10(-3) M urea. The activity is soluble and not membrane bound. It is stable at -70 C for several weeks but is more labile at higher temperatures. The pH optimum is between 5.0 and 6.0. The effect of several inhibitors on the activity was tested and revealed similarities, as well as differences, between T-strain mycoplasma urease activity and the urease activity of other organisms and plants.  相似文献   

18.
Urea concentration and urease activity in the midgut content were compared between larvae of the silkworm, Bombyx mori fed an artificial diet and those fed fresh mulberry leaves. A considerable amount of urea was found in the midgut content of the both larvae, however it was significantly lower in the larvae fed fresh mulberry leaves than in the larvae fed the artificial diet; average urea concentrations in the midgut content of the larvae fed fresh mulberry leaves and the artificial diet were 2.9 and 4.6 &mgr;mol/g, respectively. Urea in the midgut content seems to be secreted from the insect itself since the amount of urea in both diets were negligibly small. Urease activity was detected only in the midgut content of the larvae fed fresh mulberry leaves but not in other tissues of the larvae. On the other hand, no urease activity was detected in the midgut content of the larvae fed the artificial diet. Subsequently, to elucidate the role of mulberry leaf urease in the midgut lumen, larvae that had been reared on the artificial diet were switched to fresh mulberry leaves. The diet switch caused a rapid decrease in urea concentration in the midgut content and an increase in ammonia concentration in the midgut content, suggesting that secreted urea could be hydrolyzed to ammonia by mulberry leaf urease in the midgut lumen. Furthermore, to investigate the physiological significance of mulberry leaf urease on urea metabolism of the silkworm, (15)N-urea was injected into the hemocoel, and after 12 h the larvae were dissected for (15)N analysis. A considerable amount of (15)N was found to be incorporated into the silk-protein of the larvae fed fresh mulberry leaves, but there was little incorporation of (15)N into the silk-protein of the larvae fed the artificial diet. These data indicate that urea is converted into ammonia by the action of mulberry leaf urease in the midgut lumen and used as a nitrogen source in larvae fed mulberry leaves.  相似文献   

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