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1.
应用Fld_(SR)天然荧光和1,5—Br—AEDANS及5—IAF荧光探针偶标记铁蛋白和钼铁蛋白作荧光测定。Fld在与铁蛋白络合时所损失能量为铁蛋白所接受。同样,铁蛋白与钼铁蛋白络合时也有能量转移现象。铁蛋白与MgATP形成复合物后仍能将能量转移给钼铁蛋白,铁蛋白与钼铁蛋白络合物间荧光标记基团距离为35~58A,铁蛋白·MgATP与钼铁蛋白间荧光标记基因距离为38~63A。  相似文献   

2.
铁蛋白在结合MgATP时,MgATP基本上不水解,只有在与钼铁蛋白结合并传递电子给钼铁蛋白时,MgATP才酶促水解为MgADP和Pi(磷酸根),电子传递和ATP的水解是两个快速的偶联过程。[Fe_4S_4(SPh)_4]~(-2)  相似文献   

3.
应用微热量计研究了棕色固氮菌固氮酶铁蛋白与MgATP或MgADP络合的热力学状况。在25℃,1大气压下铁蛋白与MgATP饱和络合时的焓(⊿H~0)变化为-4.78千卡/摩尔,自由能(AGO)变化为-6.66千卡/摩尔,熵(⊿S~0)变化为+6.31卡·度/摩尔。在铁蛋白与MgATP络合时,随着MgATP浓度的增加,-⊿H~0也随之增加呈S型曲线,铁蛋白与MgADP饱和络合时⊿H~0为-5.45千卡/摩尔,AGO为-6.89千卡/摩尔,⊿S~0为+4.82卡·度/摩尔。熵的增加表明MgATP或MgADP与铁蛋白络合后,引起铁蛋白构型的变化。铁蛋白与MgATP或MgADP饱和络合时的TASO分别为+1.88千卡/摩尔和+1.44千卡/摩尔。  相似文献   

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固氮作用     
890921棕色固氮菌含M。一和V一固氮酶的铁蛋白〔会,英j/Bergstr6m,J.…厂7tl:In-士。rnatl.Cong.Nitrogon Fixation,Book of入bs一1988一3一22 测定T月zotobacter ehroocoee“m含MO和含V固氮酶Fe蛋白组分特性,如分子量和亚单位结构、氨基酸顺序(以nifH和HDN八序列数据得出)、Fe和S“一含显,还原态。不结合和结合MgADP和MgATI〕态的epr信号.以及生理上垂要的MgADP结合态氧化还原的中点电位。也测定了MgADP结合的氧化态还原Na:520、的动力学和需MgATP电子传递至MoFe和VFe蛋白的动力学。这些特性与MoFe和VFc蛋自“交叉反应…  相似文献   

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本文介绍了从紫色非硫光合细菌Rhodopseudomonas capsulata分离纯化的铁氧还蛋白,经固体硫酸铵分级盐析沉淀和透析进一步纯化的样品,通过循环伏安法检测其对温度的敏感性,所引起的蛋白变性;然后应用定电位电量法和电位阶跃电量法,研究它的电量-电位关系,根据Nernst公式进而计算铁氧还蛋白的中点电位分别为-378mV和-375mV,在其参与氧化-还原反应时,每分子铁氧还蛋白传递电子数目≈2。并对不同菌种来源的铁氧还蛋白的标准氧化-还原电位及其传递电子数目进行了讨论。  相似文献   

6.
本文介绍了从紫色非硫光合细菌Rhodopseudomanas capsulata 分离纯化的铁氧还蛋白,经固体硫酸铵分级盐析沉淀和透析进一步纯化的样品,通过循环伏安法检测其对温度的敏感性,所引起的蛋白变性;然后应用定电位电量法和电位阶跃电量法,研究它的电量-电位关系,根据Nernst 公式进而计算铁氧还蛋白的中点电位分别为-378mV 和-375mV,在其参与氧化-还原反应时,每分子铁氧还蛋白传递电子数目≈2。并对不同菌种来源的铁氧还蛋白的标准氧化-还原电位及其传递电子数目进行了讨论。  相似文献   

7.
鱼肝铁蛋白铁核表层接受电子能力的研究   总被引:4,自引:2,他引:2  
采用直接电化学技术研究Hong鱼肝铁蛋白(Liver Ferritin of Dasyatis akajei,DALF)铁核表层接受还原电子的快慢速率和释放铁的动力学级数及规律。实验结果表明,在有氧环境下,DALF铁核表层以两相行为的方式快速地从铂金电极上获得还原电子且用于释放铁反应,其释放铁的还原电们分别为-125mV-375mV(vs.NHE,下同)。在控制还原电位为-200mV和-500mV的条件下,DALF铁核表层解放铁的速率分别为11.1Fe^3 /(DALF.min)和33.3Fe^3 (DALF.min),因而认为DALF从铂金电极接受电子和解放铁的速率快慢与还原电位高低有关。血红素不仅能络合于DALF蛋白壳(DALFh)上,而且还能加速DALFh释放铁的速率,但无法增加DALFh释放铁的总量。DALF铁核结构中的磷铁组成存在着非均匀性。DALF铁核表层磷铁结构具有接受来自于蛋白壳电子隧道提供的还原电子能力。  相似文献   

8.
细菌铁蛋白释放铁的动力学研究   总被引:6,自引:3,他引:3  
棕色固氮菌细菌蛋白在可见光谱区中有定性的特征吸收峰。细菌铁蛋白经过量Na2S2O4还原后,该蛋白的α、β和S峰的吸光度随着蛋白还原程度增大而递增。细菌铁蛋白的氧化还原状态可分为氧化态、半还原态和深度还原态。细菌铁蛋白铁核中的磷铁组成存在着非均匀性,该蛋白释放铁核表层的铁的反应为一级反应,推测这一过程受蛋白壳中的血红素调控。细菌铁蛋白释放铁核内层的铁的反应为零级反应。  相似文献   

9.
菌体经超声破碎,高速离心,二次DEAE-52柱层析和Sephadex G-100分离纯化,得到凝胶电泳纯的细胞色素c_3。特征吸收峰在氧化态时为405,525nm;还原态时为417,520,545nm。用Sephadex G-100凝胶过滤,SDS凝胶电泳方法,测得分子量分别为12,500,13,000D。氨基酸组份分析表明最低分子量为13,500D左右。恒电位电量法测其中点电位为-364mV,参与氧化还原作用时,传递电子数目为2。氧化态时在g值为2.581,2.203,1.715处有特征的ESR波谱,还原态时,ESR波谱消失。  相似文献   

10.
王阿敬  李之望 《生理学报》1989,41(2):145-152
本文应用细胞内记录方法,对去甲肾上腺素(NA)引起蟾蜍背根神经节(DRG)神经细胞膜电位去极化或超极化反应时的膜电导及翻转电位值进行了测量,并观察了钾和钙离子通道阻断剂灌流DRG对NA引起膜电位反应的影响。当NA引起去极化反应时,15个细胞的膜电导减小32.6%。少数细胞膜电导开始增加,继而减小(n=4)。NA超极化反应时膜电导增加13.2%(n=8)。NA去极化反应的翻转电位值为-88.5±0.9mV((?)±SE,n=4),NA超极化反应在膜电位处于-89至-92mV时消失。 钾通道阻断剂四乙铵可使NA去极化幅值增加73.7±11.9%((?)±SE,n=7),并使NA超极化幅值减小40.5%(n=4)。细胞内注入氯化铯使苯肾上腺素去极化幅值增加34.5%(n=4)。钙通道阻断剂氯化锰使NA去极化及超极化反应分别减小50.5±9.9%((?)±SE,n=10)和89.5±4.9%((?)±SE,n=7)。结果提示,NA引起DRG神经细胞膜电位的去极化或超极化反应,可能与膜的钾及钙通道活动的改变有关。  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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正Dear Editor,In December 2019, a novel human coronavirus caused an epidemic of severe pneumonia(Coronavirus Disease 2019,COVID-19) in Wuhan, Hubei, China(Wu et al. 2020; Zhu et al. 2020). So far, this virus has spread to all areas of China and even to other countries. The epidemic has caused 67,102 confirmed infections with 1526 fatal cases  相似文献   

16.
Curcumin is the yellow pigment of turmeric that interacts irreversibly forming an adduct with thioredoxin reductase (TrxR), an enzyme responsible for redox control of cell and defence against oxidative stress. Docking at both the active sites of TrxR was performed to compare the potency of three naturally occurring curcuminoids, namely curcumin, demethoxy curcumin and bis-demethoxy curcumin. Results show that active sites of TrxR occur at the junction of E and F chains. Volume and area of both cavities is predicted. It has been concluded by distance mapping of the most active conformations that Se atom of catalytic residue SeCYS498, is at a distance of 3.56 from C13 of demethoxy curcumin at the E chain active site, whereas C13 carbon atom forms adduct with Se atom of SeCys 498. We report that at least one methoxy group in curcuminoids is necessary for interation with catalytic residues of thioredoxin. Pharmacophore of both active sites of the TrxR receptor for curcumin and demethoxy curcumin molecules has been drawn and proposed for design and synthesis of most probable potent antiproliferative synthetic drugs.  相似文献   

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The young pistils in the melanthioid tribes, Hewardieae, Petrosavieae and Tricyrteae, are uniformly tricarpellate and syncarpous. They lack raphide idioblasts. All are multiovulate, with bitegmic ovules. The Petrosavieae are marked by the presence of septal glands and incomplete syncarpy. Tepals and stamens adhere to the ovary in the Hewardieae and the Petrosavieae but not in the Tricyrteae. Two vascular bundles occur in the stamens of the Hewartlieae and Tricyrtis latifolia. Ventral bundles in the upper part of the ovary of the Hewardieae are continuous with compound septal bundles and placental bundles in the lower part. Putative ventral bundles occur in the alternate position in the Tricyrteae and putative placental bundles in the opposite. position in the Petrosavieae. The dichtomously branched stigma in each carpel of the Tricyrteae is supplied by a bifurcated dorsal bundle.  相似文献   

19.
Microbial resistance to antibiotics is an unresolved global concern, which needs urgent and coordinated action. One of the guidelines of the Centers for Disease Control and Preventions (CDC) to combat antibiotic resistance is the development of new antibiotics to treat drug-resistant bacteria. In our effort to find new antibiotics, we report the synthesis and antimicrobial studies of 30 new pyrazole derivatives. These novel molecules have been synthesized by using readily available starting materials and benign reaction conditions. Some of these molecules have shown activity with MIC values as low as 0.78?µg/mL against four bacterial strains; Staphylococcus aureus, methicillin-resistant S. aureus, Bacillus subtilis, and Acinetobacter baumannii. Furthermore, active molecules are non-toxic to mammalian cell line.
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