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991.
Summary Five mmol ofl-2-oxothiazolidine-4-carboxylate (OTC)/kg of body weight was administered into the stomach of rats, and cysteine levels in tissues and sulfate and taurine excreted in the urine were determined. The cysteine (plus cystine expressed as cysteine) concentration in the liver increased to 170–200% of the original level at 30 min and that in the blood to 160% at 60 min after the OTC administration. These high levels were maintained until 8 h after the administration and decreased gradually thereafter. Excretion of sulfate and taurine increased after the OTC administration and the increase corresponded to 26% and 15%, respectively, of the OTC administered. These findings suggest that at least about 40% of the OTC administered into the stomach was taken up and converted to cysteine, which was metabolized to sulfate and taurine.  相似文献   
992.
Summary Methodology for the synthesis and incorporation of-trifluoromethyl substituted amino acids into N- and C-terminal position of peptides is described. The incorporation of-trifluoromethyl substituted amino acids into strategical positions of peptides enhances proteolytic stability and lipophilicity. Furthermore, it improves transport rates in vivo and permeability through certain body barriers.  相似文献   
993.
The Alzheimer's disease βA4 amyloid precursor protein (APP) has been shown to be involved in a diverse set of biological protein precursor-like proteins (APLP1 and APLP2) belong to a superfamily of proteins that are probably functionally related. In order to characterize the cell adhesion properties of APP the brain specific isoform APP695 was purified and used to assess the binding to herparin, a structural and functional analogue of the glycosaminoglycan heparan sulfate. We show that APP binds in a time dependent and saturable manner to heparin. The salt concentration of 620 mM at which APP elutes from heparin Sepharose is greater than physiological. Tha apparent equilibrium constant for dissociation was determined to be 300 pM for APP binding to heparin Sepharose. A high affinity heparin binding site was identified within a region conversed in rodent and human APP, APLP1 and APLP2. This binding site was located between residues 316-337 of APP695 which is within the carbohydrate domain of APP. We also demonstrate an interaction between this heparin binding site and the zinc(II) binding site which is conserved in all members of the APP superfamily. We show by using an automated surface plasmon resonance biosensor (BIAcore, Pharmacia) that the affinity for heparin is increased two- to four-fold in the presence of micromolar zinc(II). The identification of zinc-enhanced binding of APP to heparin sulfate side chains of proteoglycans offers a molecular link between zinc(II), as a putative environmental toxin for Alzheimer's disease, and aggregation of amyloid βA4 protein.  相似文献   
994.
The responses of three different soil microbial communities to the experimental application of 2, 4-dichlorophenoxyacetic acid (2, 4-D) were evaluated with a variety of molecular genetic techniques. Two of the three soil communities had histories of prior direct exposure to 2, 4-D, and one had no prior direct application of any herbicide. Dominant 2, 4-D degrading strains isolated from these soils the previous year were screened for hybridization with three catabolic genes (tfdA, tfdAII, and tfdB) cloned from the well-studied 2, 4-D degradative plasmid, pJP4, revealing varying degrees of similarity with the three genes. Hybridization of total community DNA from the three soils with the tfd gene probes also indicated that pJP4-like tfd genes were not harboured by a significant percentage of the community. Community level response was evaluated by the comparison of different treatments by Random Amplified Polymorphic DNA (RAPD) fingerprints and by community DNA cross-hybridization. No differences between treatments within the same soil were detected in any of the RAPD fingerprints generated with 17 primers. Community DNA cross-hybridization also indicated that the application of 2, 4-D at the applied rates did not quantitatively affect the structure of the soil microbial communities present in the three soils during the time-frame studied.  相似文献   
995.
四川旋木雀一新亚种—天全亚种(雀形目:旋木雀科)   总被引:4,自引:1,他引:3  
本文报道了旋木雀的一新亚种,命名为旋木雀天全亚种Certhia familiaris tianquanensis,并记述了新亚种同国内已知亚种区别的形态特征。  相似文献   
996.
互叶白千层油化学成分的研究   总被引:4,自引:0,他引:4  
贾芬  黄宇翔  丁舒敏  李青   《广西植物》1995,15(4):368-370
采用水蒸汽蒸馏收集互叶白千层芳香油,对该油进行GC/MS/DS定性分析及其总离于流图的面积归一化定量分析,鉴定出25种化合物,其中含氧化合物6种,碳氢化合物19种。直接影响该油商品价值的化学成分4-萜品醇含量约为17%,桧樟脑含量约为2.4%。  相似文献   
997.
本文对高邮杂交鲫(鲫♀×白鲫♂)及其亲本血清生化组成的定量分析。结果表明,在测定的血清总蛋白、白蛋白、胆固醇、尿素氮、葡萄糖、乳酸脱氢酶、a-羟丁酸脱氢酶、a-淀粉酶和谷草转氨酶等九个生化指标中,大部分指标高邮杂交鲫与母本无显著差异,而与父本则有极显著差异。这从代谢方面论证了高邮杂交鲫是一个偏向于母本的杂交种。  相似文献   
998.
调查了原籍华北地区汉族的ABO、Lewis、MN、Rh、P等血型系统和ABH分泌型的分布,结果表明:O型(33.44%)和B型(29.38%)较多;N型(27.97%)略多于M型(27.65%);Le(a )型的频率很高(24.17%)。在94人中还发现四名Le(a )型属于ABH分泌型,且都属于分泌A或B血型物质的类型,无一例为分泌H血型物质的类型;Rh(D)阴性率仅0.3%,CCDee和CcDE型占75%以上;P_1( )型占39.1%;ABH分泌型占72%,低于全国其他民族中已知的分布。  相似文献   
999.
Abstract The aims of this work were to discover the distribution within the C4 grass Spartina anglica of a PEP carboxylase which is very unstable during and after extraction, and to determine whether this unstable form occurs in other members of the genus. In S. anglica, only the leaf contains an unstable PEP carboxylase. Within the leaf only the major one of two isoenzymes is unstable, and this is located in the mesophyll cells. The unstable isoenzyme is inactivated during extraction and storage unless protected by bovine serum albumin or Triton X-100, and is inactivated in assay mixtures at optimum pH in the absence of PEP. Evidence is presented that inactivation is not due to degradation or inhibition during extraction and storage. The enzyme from leaves of Spartina species taxonomically closely related to S. anglica is also very unstable during and after extraction, but that from less closely related species is much more stable.  相似文献   
1000.
M E Hall  J M Stewart 《Peptides》1984,5(1):85-89
Substance P (SP) significantly reduced fighting in mice made aggressive by prolonged isolation. The N-terminal heptapeptide fragment SP (1-7) also reduced fighting. The C-terminal fragment SP(4-11) was without activity, while the shorter C-terminal fragment analog less than E-SP(7-11) significantly increased isolation-induced fighting. The aggression-enhancing effect of less than E-SP(7-11) was antagonized by naloxone, which by itself had no significant effect. The aggression-reducing effect of SP(1-11) was significantly enhanced by naloxone, while the effect of SP(1-7) was unchanged. These results demonstrate that a behavioral effect of SP may be duplicated by an N-terminal fragment of the SP molecule, and that peptide fragments or analogs of the N- and C-terminal portions of the SP molecule can exert opposing effects on a specific behavior. These findings represent a structure/activity relationship that is strikingly different from any previously described for SP. The differing effects of naloxone on N- and C-terminal fragment analogs suggest that these two effects may be mediated by different mechanisms.  相似文献   
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