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1.
硅藻土在青霉素G酰化酶提纯中的应用   总被引:1,自引:0,他引:1  
国产硅藻土经氢氧化铵处理后可用于从发酰液中直接取青霉素G酰化酶,平均吸附量为90U/g。吸附的酶可用22%硫酸胺-0.3mol/L PBS(pH8.0)溶液洗脱。平均比活18U/mg蛋白(NIPAB法)。硅藻土可反复使用。苯乙酰胺-Sepharose 4B树脂可对酶作进一步的纯化。  相似文献   

2.
用STN(含蔗糖,0.4mol/L;NaCl,0.01mol/L和Tris-HCl,0.02mol/L,pH7.4)提取的菠菜叶片叶绿体再用STN洗涤后,它的内源无机磷酸盐含量急剧减少,其Mg2+-ATP酶水解ATP的能力明显下降。进一步研究表明:叶绿体的内源无机磷酸盐含量减少会使反映叶绿体类囊体膜内外△pH变化的9-氨基吖啶的荧光猝灭减少,并加速光激活态ATP酶的暗失活。  相似文献   

3.
国产硅藻土经氢氧化铵处理后可用于从发酰液中直接取青霉素G酰化酶,平均吸附量为90U/g。吸附的酶可用22%硫酸铵-0.3mol/LPBS(pH8.0)溶液洗脱。平均比18U/18Umg蛋白(NIPAB法)。硅藻土可反复使用。苯乙酰胺-Sepharose4B树脂可对酶作进一步的纯化。  相似文献   

4.
蚯蚓体内一种纤溶酶原激活剂(e-PA)对ATEE的降解   总被引:3,自引:0,他引:3  
赤子爱胜蚓(Eiseniafetida)体内的一种纤溶酶原激活剂(e-PA)能够降解人工合成底物N-乙酰-L-酪氨酸乙酯(ATEE),该降解反应的最适pH为8.5,而且在0.2mol/LNa2HPO4中的活性要强于在0.05mol/LTris-HCl(pH8.5)中.分别测定了e-PA的大小亚基及全酶在0.2mol/LNa2HPO4与0.05mol/LTris-HCl(pH8.5)两种体系中的Km和Kcat.结果表明,在0.2mol/LNa2HPO4中,全酶的ATEE活性远远高于大小亚基单独的ATEE活性,而在0.05mol/LTris-HCl(pH8.5)中则没有这种现象.从蛋白质结构的角度对这一结果作了解释.用不同抑制剂和e-PA作用,结果表明,pepstatin,E-64和EDTA对e-PA的ATEE活性都有不同程度的抑制,这一点与e-PA的BAEE活性不同.  相似文献   

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将KGM和Sepharose 4B凝胶在相同条件下活化、偶联接上染料Cibacron Blue F3GA制成了KGM和Sepharose 4B染料亲和吸附剂,并用来与牛血甭白蛋白(BSA)作用,每毫升KGM亲和吸附剂可吸附BSA 28mg,用NaSCN洗脱时间为84.5%,而Sepharose 4B染料样和吸附剂每毫升可吸附BSA 15.3mg,用NaSCN洗脱时间收迷81.7%,并对两种凝胶的染  相似文献   

6.
盐生杜氏藻甘油-3-磷酸脱氢酶的分离纯化及其特性的研究   总被引:1,自引:0,他引:1  
利用PEG分级,DEAE离子交换层析,BlueSepharose拟亲和层析,MonoQ离子交换层析等手段,分离纯化盐生杜氏藻(Dunalielasalina(Dunal)Teod.)甘油三磷酸(G3P)脱氢酶(EC1.1.1.8),得到比活为12.6U/mg的电泳纯的酶,并对此酶的生化特性进行了研究。4%~20%非变性聚丙烯酰胺梯度凝胶电泳测得全酶分子量约为270kD,SDSPAGE表明该酶只有一种分子量约为65kD的亚基,据此推测该酶应为同四聚体。酶催化磷酸二羟丙酮(DHAP)还原的最适pH值为7.5,催化G3P脱氢的最适pH值为10。该酶对4个底物还原型辅酶Ⅰ(NADH),二磷酸吡啶核苷酸(DHAP),辅酶Ⅰ(NAD),G3P的表观Km值分别为63μmol/L,272μmol/L,1.53mmol/L,6.52mmol/L。该酶在保存过程中易失活。NADH能降低酶失活的速度,而NAD则不然。低浓度NaCl对酶略有保护作用,但高浓度NaCl加快酶的失活,且浓度越高效应越明显。  相似文献   

7.
链霉菌Z94-2碱性脂肪酶产生条件及酶学性质   总被引:2,自引:0,他引:2  
在152 株脂肪酶产生菌中,链霉菌Z942 产脂肪酶活力为596u/ mL,其最适培养基(g/L) 为:糊精10 、黄豆饼粉30 、尿素10 、K2HPO4 0-5 、MgSO4 0-5 、NaCl 1 和AEO9 0 .5 ,产酶的最适条件为:初始pH9 .5 ~10-0 ,在26 ℃培养48h 。用PVA 橄榄油乳化系统测定该酶的最适pH9 .8 ,最适温度37 ℃,在pH8-6 ~10-2 于5 ℃存放24 h ,酶活力不变。0-14mol/L 的氯化钙有较大的激活作用。  相似文献   

8.
本文从含ArgRS306KR基因args306KR的pUC18重组质粒的大肠杆菌TG1转化子中经DEAE-Sephacel和Blue-Sepharose两步柱层析,得到电泳一条带的ArgRS306KR。纯酶的比活为2790单位/毫克。该酶氨酰化和ATP~PPi交换活力的最适pH分别为pH8.3和pH7.5。氨酰化活力对ATP、Arg和tRNA的Km分别为2.6mmol/L、14.0μmol/L和5.0μmol/L:Vmax为7630单位/毫克;koat为9S-1。ATP~PPi交换活力对ATP和Arg的Km分别为8.3mmol/L和99μmol/L;Vmax为16320单位/毫克;kcat为18S-1。  相似文献   

9.
用分子筛(岛津DIOL-150柱)和阳离子交换(岛津WCX-1柱)高效液相色谱从虎纹捕鸟蛛(Selenocosmiahuwena)毒液中分离提纯透明质酸酶(Hyaluronidase,EC3.2.1.35).经等电聚焦电泳为一条带,pI=7.2.经SDS-聚丙烯酰胺凝胶电泳测得分子量为40kD,经凝胶过滤测得分子量为40.7kD。以透明质酸为底物时在pH3.5─5.5范围内有较大活性,最适pH值为4.0;在pH4.5─6.0范围内稳定,在反应温度为30─60℃时有较大活性,最适温度为50℃;对热稳定,0.15mol/L的NaCl对酶活性有一定的稳定作用.3%的肝素、500μmol/L的Hg~(2+)、Fe~(2+)、Cu~(2+)对酶活性有明显的抑制作用。  相似文献   

10.
从CHO工程细胞培养上清初步纯化的uPA免疫BALB/c小鼠,通过杂交瘤技术制备单克隆抗体细胞株,取其中一株38-1-7株作高密度大量培养,细胞密度达13.2×106/mL时,抗体滴度为1∶61.44×104。用自制的uPA-Sepharose4B柱纯化抗体。抗体滴度提高243倍。纯化后的抗体与活化的Sepharose4B珠交联,制成IgG-Sepharose4B亲和层析抗体柱,亲和力常数:1.28×109(mol/L)-1,交联率:83.5%。直接从培养上清纯化uPA,纯度为96.3%,回收率:81.6%±19,纯化倍数:50倍左右,比活1.11±0.29×105。试验结果表明该法效果好,方法简单、操作方便、值得进一步研究和应用。  相似文献   

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It has now been over twenty years since a novel herpesviral genome was identified in Kaposi's sarcoma biopsies. Since then, the cumulative research effort by molecular biologists, virologists, clinicians, and epidemiologists alike has led to the extensive characterization of this tumor virus, Kaposi's sarcoma-associated herpesvirus(KSHV; also known as human herpesvirus 8(HHV-8)), and its associated diseases. Here we review the current knowledge of KSHV biology and pathogenesis, with a particular emphasis on new and exciting advances in the field of epigenetics. We also discuss the development and practicality of various cell culture and animal model systems to study KSHV replication and pathogenesis.  相似文献   

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Comprises species occurring mostly in subtidal habitats in tropical, subtropical and warm-temperate areas of the world. An analysis of the type species, V. spiralis (Sonder) Lamouroux ex J. Agardh, a species from Australia, establishes basic characters for distinguishing species in the genus. These characters are (1) branching patterns of thalli, (2) flat blades that may be spiralled on their axis, (3) width of the blade, (4) primary or secondary derivation of sterile and fertile branchlets and (5) position of sterile and fertile branchlets on the thalli. Application of the latter two characters provides an important basic method for separation of species into three major groups. Osmundaria , a genus known only in southern Australia, was studied in relation to Vidalia , and its separation from the Vidalia assemblage is not accepted. Species of Vidalia therefore are transferred to the older genus name, Osmundaria. Two new species, Osmundaria papenfussii and Osmundaria oliveae are described from Natal. Confusion in the usage of the epithet, Vidalia fimbriala Brown ex Turner has been clarified, and Vidalia gregaria Falkenberg, described as an epiphyte on Osmundaria pro/ifera Lamouroux, is revealed to be young branches of the host, Osmundaria prolifera.  相似文献   

17.
Fifteen chromosome counts of six Artemisia taxa and one species of each of the genera Brachanthemum, Hippolytia, Kaschgaria, Lepidolopsis and Turaniphytum are reported from Kazakhstan. Three of them are new reports, two are not consistent with previous counts and the remainder are confirmations of very scarce (one to four) earlier records. All the populations studied have the same basic chromosome number, x = 9, with ploidy levels ranging from 2x to 6x. Some correlations between ploidy level, morphological characters and distribution are noted.  相似文献   

18.
肝癌中HBV和HCV基因和抗原的分布及意义   总被引:1,自引:0,他引:1  
采用原位分子杂交方法检测HCV RNA及HBV X基因;采用免疫组织化学方法研究HCV核心抗原,非结构区C33c抗原及HBxAg在肝细胞肝癌中的定位及分布.结果表明(1)HCV RNA、HBV X基因在肝细胞肝癌组织检出率分别为40%(55/136)和82%(112/136).HCV RNA定位于癌细胞的胞浆内,阳性细胞呈散在、灶状及弥漫分布三种形式;HBV X基因在肝癌细胞中的分布呈胞浆型、核型及核浆型,阳性细胞也呈上述三种分布形式;(2)HCV C33c抗原、核心抗原在肝细胞肝癌中的阳性率为81%(133/164)及86%(141/164).C33c抗原定位于癌细胞及肝细胞的胞浆内;核心抗原既定位于癌细胞核中,又可定位于胞浆中.C33c抗原阳性细胞以灶状分布为主;而核心抗原阳性细  相似文献   

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For a plant selection model with frequency-independent viabilities, fertilities and selfing rates, it is shown that apart from global fixation, for certain parameter combinations a protected polymorphism and facultative fixation (either allele may become fixed according to initial frequencies) may both occur. Facultative fixation requires different selling rates for the dominant and recessive type. Protection of the polymorphism requires resource allocation for male and female function. In this connection the problem of purely genetically caused population extinction is discussed.
For general frequency dependence and regular segregation, the chances for establishment of a completely recessive gene are compared to those of a completely dominant gene. It is proven that the process of establishment of the recessive gene, despite a fitness advantage, may be considerably endangered by drift effects if random mating prevails. The recessive gene may reach the same effectivity in establishment as a dominant gene, only if the recessive homozygote mates exclusively with its own type during the period of establishment.  相似文献   

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