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1.
碳酸酐酶CA(EC 4.2.1.1)是含锌原子的金属蛋白酶,该酶的基本功能是催化CO2与HCO3-间的相互转换[1].该反应在许多生物过程中都发挥着重要的作用,例如离子交换、呼吸作用、pH稳定性、捕获CO2和光合作用等[2~5].CA广泛分布于各种生物中,已知的CA酶根据氨基酸序列被分为-αCA,-βCA和γ-CA三种类型[5~7].这3种类型的CA酶序列间的相似性很低,被认为是由不同的途径进化而来的[7].α-型的CA酶在动物、植物、绿藻、细菌和蓝细菌中都有发现[7],在藻类中报道的α-型CA还很少.迄今为止只在衣藻中发现2种异构体,在盐藻中发现3种[8,9],在红藻中还未见报道. 相似文献
2.
J. SELVERSTONE 《Journal of Metamorphic Geology》2005,23(6):461-470
Interlayered graphitic and non‐graphitic schists from the Tauern Window, Eastern Alps, record contrasting mechanical behaviour during extensional exhumation. Graphitic schists contain mesoscale extension fractures, pervasive microcracks in garnet, and abundant secondary fluid inclusion planes; all three types of structures are oriented perpendicular to the stretching lineation. Crack spacings in garnet from graphitic samples are tightly clustered around a mean of 180 μm. Non‐graphitic schists have fewer and more randomly oriented microcracks and fluid inclusion planes and maintained strain compatibility via crystal plasticity. The presence or absence of graphite appears to have exerted a fundamental control on rheology during unroofing. Calculations for a model graphitic rock at 500 °C and fO2 = 10?24 MPa show that the equilibrium metamorphic fluid evolves from XCO2 = 0.07 to 0.38 during decompression from 700 to 400 MPa, in agreement with microcrack fluid inclusion data that show a change from XCO2 < 0.1 to 0.45 in graphitic samples over the same pressure interval. This compositional shift results in >60% expansion of the pore fluid during decompression. H2O‐rich fluid in non‐graphitic rocks expands <15% over the same pressure interval. The greater pore fluid expansion in low‐permeability graphitic horizons likely promoted tensile failure during unroofing. These results suggest that microcracking should be an inevitable consequence of decompression in many graphitic schists, whereas rocks that lack graphite are less likely to undergo microcracking. Microseismicity is predicted to be more common in graphitic than non‐graphitic rocks during unroofing of mountain belts. 相似文献
3.
CO2向H^ 和HCO3^－的转换是一相对慢速过程。因此，其动力学可能决定碳酸盐岩的溶解速率。在灰岩和白云岩的溶解实验中，使用了自然界普遍存在的碳酸酐酶（CA）来催化这一CO2转换反应，结果发现，对灰岩而言，加入CA后，其溶解速率在高CO2分层时可增加10倍，而对白云岩，其溶解速率增加主要在低CO2分压时，可达3倍左右。这一发现表明，化学风化（包括碳酸盐岩溶解和硅酸盐风化）作用在大气CO2沉降和全球碳循环里的所谓丢失的汇中的重要性需要重新评价。毫无疑问，已往的研究由于未认识到CA在风化中的催化作用，因此低估了风化作用的速率，同时也低估了风化作用对大气CO2沉降的贡献。另一方面，也表明了研究自然界不同水体中CA分布及其活度和CA在自然界风化作用中的作用的必要性。 相似文献
4.
A simulation was undertaken within a climatic chamber to investigate limestone dissolution under varied carbonic acid (H2CO3) strengths as a possible analogue for future increases in atmospheric CO2 arising from global warming. Twenty‐eight samples cut from a block of Bath (Box Hill) limestone from Somerville College, Oxford, which had been removed during restoration after 150 years in an urban environment, were weighed and placed in closed bottles of thin plastic containing varying concentrations of H2CO3. Half of the stone samples were derived from exposed surfaces of the stone block (weathered) while the others were obtained from the centre of the block on unexposed surfaces (unweathered). The purpose of this was to compare dissolution of previously weathered versus unweathered surfaces in strong (pH 4·73) versus weak (pH 6·43) solutions of H2CO3. A temperature of c. 19 °C was maintained within the chamber representing a plausible future temperature in Oxford for the year 2200 given current warming scenarios. The simulation lasted 25 days with a few stone samples being removed midway. Stone samples show reduced weight in all cases but one. There was greater dissolution of stone samples in a strong H2CO3 solution as conveyed by higher concentrations of total hardness and Ca2+ in the water samples as well as enhanced microscopic dissolution features identified using SEM. The simulation confirms that enhanced atmospheric CO2 under global warming, given adequate moisture, will accelerate dissolution rates particularly of newly replaced limestone building stones. However, previously weathered surfaces, such as those on historical stone exposed for a century or more, appear to be less susceptible to the effects of such increased rainfall acidity. Conservation techniques which remove weathered surfaces, such as stone cleaning, may accelerate future decay of historical limestone structures by increasing their susceptibility to dissolution. Copyright © 2006 John Wiley & Sons, Ltd. 相似文献
5.
以非岩溶区林地为对比,分析了桂林毛村岩溶区4种不同植被类型土壤微生物数量及碳酸酐酶(CA)活性的季度动态变化规律,发现以下主要结果:1随着植被的正向演替,岩溶区弃耕地、草地、灌丛及林地微生物数量及CA活性逐渐升高,微生物总数从64.07×10~4cfu/g上升到178.23×10~4cfu/g,CA活性从0.77 U/g上升到1.82 U/g,岩溶区林地大于非岩溶区林地。2在岩溶区不同植被类型,微生物组成均表现为细菌最多(平均值95.14%),放线菌次之(平均值2.79%),真菌数量最少(平均值1.75%)。而在非岩溶区表现为细菌最多(平均值90.95%),真菌次之(平均值5.32%),放线菌最少(平均值3.73%)。3微生物数量季节动态整体表现为春季至夏季逐渐上升,至秋季达到最高,冬季下降,微生物总数的增长依赖于细菌的倍数增长,真菌和放线菌影响较小。CA活性整体表现为夏季和冬季低于春季和秋季,秋季达到最大值。4 CA活性与细菌及微生物总数呈极显著的正相关,表明土壤CA主要来源于细菌的分泌。 相似文献
6.
阿尔泰大东沟铅锌矿的碳质流体及其成因 总被引：5，自引：0，他引：5
大东沟铅锌矿是阿尔泰南缘泥盆纪克朗火山-沉积盆地的块状硫化物矿床之一,在石炭—二叠纪同造山的区域变质过程中,受到热液叠加改造作用,层状铅锌矿体发育脉状石英和矿化。本文对阿勒泰大东沟铅锌矿区石英脉中的包裹体进行了详细的岩相学和显微测温研究,估算出包裹体形成时的物理化学条件,并采用激光拉曼、同步辐射X射线荧光(SRXRF)对流体包裹体进行了成分测试。结果显示,石英脉中的包裹体主要为碳质流体包裹体,多以面状、带状分布,最低捕获温度在209～459℃之间,密度为0.75～1.15g/cm3,最低捕获压力在110～540MPa之间。初步研究表明碳质流体的来源与同造山的变质作用有关,而与海底喷流沉积无关。激光拉曼测试结果表明包裹体气液主要成分为CO2和N2。SRXRF测试碳质包裹体中金属微量元素显示低Cu、Zn、Pb,而富集Au。 相似文献
7.
以贵州普定喀斯特石漠化区域石生银叶真藓（Bryum argenteum Hedw.）、扭口藓（Barbula unguiculata Hedw.）、穗枝赤齿藓（Erythrodontium julaceum(Schwaegr.)Par.）、美灰藓（Eurohypnum leptothollum(C. Muell. )Ando.）、东亚砂藓（Racomitrium japonicum Dozy et Molk.）和雪茶（地衣）（Thamnolia vermicularia(Ach.)Asa-hina）为对象,研究了这些石生植物和其基质土壤碳酸酐酶（CA）的活性,可为石生植物的生物岩溶作用机理和石漠化生态环境的治理提供一定的参考。结果表明,6种植物CA的活性存在一定的差异,以美灰藓的CA活性272.99 U·g-1(FW)最高,东亚砂藓的CA活性33.45 U·g-1(FW)最低;银叶真藓基部土壤CA活性最高,为101.81 U·g-1(干土),美灰藓CA活性15.95 U·g-1(干土)最低。CA活性与土壤全磷、全钾、石砾含量和土壤含水量之间呈极显著的相关性。 相似文献
8.
一株产碳酸酐酶附生菌对铜绿微囊藻(Microcystis aeruginosa)生长的影响 总被引：1，自引：1，他引：0
为研究生长环境中微生物对铜绿微囊藻碳代谢的影响,本文分析太湖典型微囊藻水华样品附生菌中产碳酸酐酶(CA)细菌的比例,结果显示CA菌占11.6%;从微囊藻群体中分离获得了一株高胞外CA附生菌P201,通过ITS基因鉴定,该菌为一株荧光假单胞菌(Pseudomonas fluorescence).并研究了该菌在不同浓度HCO3-条件下对铜绿微囊藻生长的影响,结果表明无论是高HCO3-浓度还是低HCO3-浓度环境中,加入该菌对铜绿微囊藻的生长均有促进作用,说明产CA酶附生菌对铜绿微囊藻的生长有一定的促进作用. 相似文献
9.
为了探讨流域岩溶生态系统土壤碳酸酐酶(CA)活性、有机碳含量及CA固碳之间的潜在关系,选取长江流域干流及支流沿岸不同地质生态环境下的10个样地,比较长江流域不同地质生态环境下表层土壤(0~20cm)中的碳酸酐酶(CA)活性与土壤有机碳(SOC)含量,并分析二者之间的关系。结果表明:(1)长江流域岩溶区的表层土壤CA活性要高于非岩溶区(P0.01),土壤CA活性的差异与样地的地质类型及植被类型不同有关;(2)位于岩溶区高场(GC)样地的年平均SOC含量最高(1.09%),而位于非岩溶区外洲(WZ)样地的年平均SOC含量最低(0.29%),而且总体比较而言,长江流域冬季表层土壤的平均SOC含量显著高于夏季(P0.01);(3)相关性分析结果显示,不同季节长江流域岩溶区表层土壤CA活性与SOC含量呈一定的正相关。研究结果为进一步研究流域岩溶生态系统土壤CA与土壤固碳能力之间的关系奠定了基础。 相似文献
10.
为了探究海带(Saccharina japonica)α-CA1和α-CA2是否具有催化CO2的可逆水合反应和酯酶活性,作者通过原核表达得到这两种α-CA的可溶性的异源重组蛋白。分别用电极法和酯酶活性检测法来检测重组α-CA1(rα-CA1)和rα-CA2的水合酶活性和酯酶活性,结果发现,rα-CA1的水合酶活性(1.52±0.120 U/mg)几乎是rα-CA2(0.54±0.046 U/mg)的3倍,表明rα-CA1催化CO2的水合能力明显大于rα-CA2。而两者的酯酶活性并没有显著的差别(rα-CA1比活力:0.697±0.176 U/g,rα-CA2比活力:0.743±0.129 U/g),说明催化乙酸对硝基苯酯(p-NPA)生成对硝基苯酚(p-NP)的能力是没有显著差别的。实验结果证实这2个α-CA为功能蛋白,可能参与海带无机碳吸收和储存过程,因此,本研究为海带无机碳吸收和储存机制的解析提供了生物化学依据。 相似文献