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Elevation of hyperoxia of thymidine kinase activity in hypertrophic V79 lung fibroblasts. 肥厚性V79肺成纤维细胞胸苷激酶高氧活性的升高。
Enzyme Pub Date : 1990-01-01 DOI: 10.1159/000468699
S K Das, B L Fanburg
{"title":"Elevation of hyperoxia of thymidine kinase activity in hypertrophic V79 lung fibroblasts.","authors":"S K Das,&nbsp;B L Fanburg","doi":"10.1159/000468699","DOIUrl":"https://doi.org/10.1159/000468699","url":null,"abstract":"<p><p>Exposure of V79 cells to hyperoxia (80% O2) for 30 h increased the level of thymidine kinase, a deoxynucleoside salvage enzyme, by approximately 3-fold as compared to cells exposed to room air, but did not cause any significant change in deoxycytidine kinase, the other known deoxynucleoside salvage enzyme. Exposure of cells to anoxia, on the other hand, produced only a slight reduction in thymidine kinase activity. Perturbation in cellular metabolism following exposure to hyperoxia was indicated by marked inhibition of cellular growth and the presence of cellular hypertrophy. Although growth was also inhibited by anoxia, the cell size distribution was minimally altered. The effect of hyperoxia on thymidine kinase suggests that (1) this enzyme may play a role in the modulation of cellular hypertrophy and function following exposure to hyperoxia, and (2) analysis of relative levels of thymidine kinase and deoxycytidine kinase activities may be of value in differentiating between cellular hypertrophy and hyperplasia under some circumstances.</p>","PeriodicalId":11933,"journal":{"name":"Enzyme","volume":"43 1","pages":"1-9"},"PeriodicalIF":0.0,"publicationDate":"1990-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1159/000468699","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"13510343","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 2
In vitro regulation of rat liver L-threonine deaminase by different effectors. 不同效应物对大鼠肝脏l -苏氨酸脱氨酶的体外调节作用。
Enzyme Pub Date : 1990-01-01 DOI: 10.1159/000468718
R Pagani, R Leoncini, L Terzuoli, R Guerranti, E Marinello
{"title":"In vitro regulation of rat liver L-threonine deaminase by different effectors.","authors":"R Pagani,&nbsp;R Leoncini,&nbsp;L Terzuoli,&nbsp;R Guerranti,&nbsp;E Marinello","doi":"10.1159/000468718","DOIUrl":"https://doi.org/10.1159/000468718","url":null,"abstract":"<p><p>The regulation of liver L-threonine deaminase by different effectors--bile acids, bile pigments and monocarbon molecules--was investigated. Total inhibition of the enzyme was observed with physiological concentrations of bile acids and biliverdin. Purely competitive inhibition of the holoenzyme by several monocarbon molecules was demonstrated; the mechanism was partially competitive for bicarbonate. Inhibition was more pronounced in the case of the dialyzed enzyme. From the higher Km values for pyridoxal-5'-phosphate (PLP), obtained in the presence of the inhibitors, the results are explained on the basis of interference in the association reaction: apoprotein + PLP----holoenzyme. The various effects determined by bicarbonate may play a specific role in vivo since they occur at physiological concentrations of this compound.</p>","PeriodicalId":11933,"journal":{"name":"Enzyme","volume":"43 3","pages":"122-8"},"PeriodicalIF":0.0,"publicationDate":"1990-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1159/000468718","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"13283585","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 2
Overview: phosphorylation and translation control. 概述:磷酸化和翻译控制。
Enzyme Pub Date : 1990-01-01 DOI: 10.1159/000468744
J W Hershey
{"title":"Overview: phosphorylation and translation control.","authors":"J W Hershey","doi":"10.1159/000468744","DOIUrl":"https://doi.org/10.1159/000468744","url":null,"abstract":"<p><p>Protein synthesis is controlled by the phosphorylation of proteins comprising the translational apparatus. At least 12 initiation factor polypeptides, 3 elongation factors and a ribosomal protein are implicated. Stimulation of translation correlates with enhanced phosphorylation of eIF-4F, eIF-4B, eIF-2B, eIF-3 and ribosomal protein S6, whereas inhibition correlates with phosphorylation of eEF-2 and the alpha-subunit of eIF-2. Strong evidence for regulatory roles exists for eIF-2, eIF-4F and eEF-2, whereas changes in other factor activities due to phosphorylation remain to be demonstrated. Regulation of the specific activity of the translational apparatus by phosphorylation appears to be a general mechanism for the control of rates of global protein synthesis, and may also play a role in modulating the translation of specific mRNAs.</p>","PeriodicalId":11933,"journal":{"name":"Enzyme","volume":"44 1-4","pages":"17-27"},"PeriodicalIF":0.0,"publicationDate":"1990-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1159/000468744","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"13288332","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 31
Translationally regulated genes in higher eukaryotes. 高等真核生物中翻译调控的基因。
Enzyme Pub Date : 1990-01-01
{"title":"Translationally regulated genes in higher eukaryotes.","authors":"","doi":"","DOIUrl":"","url":null,"abstract":"","PeriodicalId":11933,"journal":{"name":"Enzyme","volume":"44 1-4","pages":"1-346"},"PeriodicalIF":0.0,"publicationDate":"1990-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"13288425","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Maternal mRNA expression in early development: regulation at the 3' end. 母体mRNA在发育早期的表达:在3'端调控。
Enzyme Pub Date : 1990-01-01 DOI: 10.1159/000468753
J D Richter, J Paris, L L McGrew
{"title":"Maternal mRNA expression in early development: regulation at the 3' end.","authors":"J D Richter,&nbsp;J Paris,&nbsp;L L McGrew","doi":"10.1159/000468753","DOIUrl":"https://doi.org/10.1159/000468753","url":null,"abstract":"<p><p>Early development in many animals is programmed by maternal mRNAs inherited by the fertilized egg. Many of these RNAs are translationally dormant in immature oocytes, but are recruited onto polysomes during meiotic maturation or fertilization. Polyadenylation plays a major role in controlling the translation of maternal mRNA during these times of development. Polyadenylation, in turn, is dependent upon two cis elements that reside in the 3'-terminal region of responsive mRNAs. In two cases, the factors that interact with these regions have been examined. The half-life of maternal mRNA also is regulated by polyadenylation, which again is controlled by 3'-terminal cis elements. The recent literature covering these topics is reviewed.</p>","PeriodicalId":11933,"journal":{"name":"Enzyme","volume":"44 1-4","pages":"129-46"},"PeriodicalIF":0.0,"publicationDate":"1990-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1159/000468753","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"13288428","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 14
delta-Aminolevulinic acid dehydratase: is there a form unique to renal cortex? 氨基乙酰丙酸脱水酶:是否有肾皮质独有的形式?
Enzyme Pub Date : 1990-01-01 DOI: 10.1159/000468701
K S Roth, P D Spencer, L C Moses, B E Carter
{"title":"delta-Aminolevulinic acid dehydratase: is there a form unique to renal cortex?","authors":"K S Roth,&nbsp;P D Spencer,&nbsp;L C Moses,&nbsp;B E Carter","doi":"10.1159/000468701","DOIUrl":"https://doi.org/10.1159/000468701","url":null,"abstract":"<p><p>Succinylacetone (SA) is known to be a potent inhibitor of delta-aminolevulinic acid dehydratase (ALAD) in the liver. We have examined the effects of SA on the rat renal cortical enzyme, our observations indicating very different behaviour of renal versus hepatic ALAD with SA treatment. While the temperature response of ALAD in both tissues was similar, addition of 4 mmol/l SA inhibited liver ALAD at 37 and 55 degrees C and enhanced renal ALAD activity 2- to 3-fold at each temperature. This increase in renal ALAD was progressive with SA concentrations form 1 to 10 mmol/l. A pH titration curve for both liver and kidney ALAD showed the hepatic enzyme to have a single pH optimum, while the renal enzyme had two, each of which was distinct from that in liver. Kinetic studies with and without 4 mmol/l SA over a 50-fold ALA concentration range indicated SA-induced enhancement of renal ALAD over the entire range at both pH optima. Using 14C-labelled ALA, we have confirmed these observations made on the basis of a colorimetric assay for PBG, the enzyme product. We conclude that renal ALAD may be a different molecular species from the liver enzyme. Further studies may clarify the significance of these observations to renal heme synthesis.</p>","PeriodicalId":11933,"journal":{"name":"Enzyme","volume":"43 1","pages":"17-25"},"PeriodicalIF":0.0,"publicationDate":"1990-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1159/000468701","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"13510344","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 4
Effect of alcohol on lipoprotein metabolism. II. Lipolytic activities and mixed function oxidases. 酒精对脂蛋白代谢的影响。2脂溶活性和混合功能氧化酶。
Enzyme Pub Date : 1990-01-01 DOI: 10.1159/000468704
J G Parkes, W Auerbach, D M Goldberg
{"title":"Effect of alcohol on lipoprotein metabolism. II. Lipolytic activities and mixed function oxidases.","authors":"J G Parkes,&nbsp;W Auerbach,&nbsp;D M Goldberg","doi":"10.1159/000468704","DOIUrl":"https://doi.org/10.1159/000468704","url":null,"abstract":"<p><p>The mechanism by which alcohol increases plasma total high density lipoproteins (HDLs) and HDL-cholesterol is unknown, but it may involve modulation of the lipolytic enzymes, hepatic triglyceride lipase (HTGL) and/or lipoprotein lipase (LPL) in hepatic and extrahepatic tissues. The modulation of HDL metabolism by alcohol may also be related to its potential to induce mixed function oxidases in liver microsomes. These possibilities were examined by a pair-feeding protocol in which rats were fed diets with 35% of the caloric content as ethanol; control groups received a diet with an isocaloric amount of sucrose or were fed chow ad libitum. Alcohol caused a significant decrease in HTGL activity of liver microsomes, but there was no significant effect of alcohol upon the activities of LPL in adipose tissue and heart muscle. The relative rates of mixed function oxidases, assayed in control liver microsomes using ethoxy-,pentoxy- and benzyloxy-resorufin as substrates, were benzyloxy greater than ethoxy greater than pentoxy. This order was not affected by alcohol, but the oxidation of ethoxy- and pentoxyresorufin was reduced in liver microsomes from the ethanol-fed group. HTGL synthesis and secretion were also measured using primary rat hepatocyte cultures isolated from animals on the above dietary regimes and maintained for up to 3 days in basal medium alone or supplemented with 10 mmol/l ethanol. In basal media the order of activity of extracellular HTGL, released by the addition of heparin, was sucrose-fed greater than chow-fed greater than ethanol-fed. The rate of HTGL secretion from hepatocytes was stimulated in ethanol-containing medium, and was greater in hepatocytes from the sucrose-fed controls.(ABSTRACT TRUNCATED AT 250 WORDS)</p>","PeriodicalId":11933,"journal":{"name":"Enzyme","volume":"43 1","pages":"47-55"},"PeriodicalIF":0.0,"publicationDate":"1990-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1159/000468704","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"13510345","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 21
Acid lability of the mutated glucosylceramide-beta-glucosidase in a lymphoid cell line from type 2 Gaucher disease. 2型戈谢病淋巴样细胞系中突变的葡萄糖神经酰胺- β -葡萄糖苷酶的酸不稳定性。
Enzyme Pub Date : 1990-01-01 DOI: 10.1159/000468712
A Maret, R Salvayre, M Troly, L Douste-Blazy
{"title":"Acid lability of the mutated glucosylceramide-beta-glucosidase in a lymphoid cell line from type 2 Gaucher disease.","authors":"A Maret,&nbsp;R Salvayre,&nbsp;M Troly,&nbsp;L Douste-Blazy","doi":"10.1159/000468712","DOIUrl":"https://doi.org/10.1159/000468712","url":null,"abstract":"<p><p>Lymphoid cell lines from patients with infantile (type-2) and juvenile (type 3) Gaucher disease have been established by Epstein-Barr virus transformation and investigated and compared with the adult phenotype (type 1) with the view to enzymology. The enzymatic defect in glucosylceramide(GlcCer)-beta-glucosidase activity was more severe in type 2 and 3 than in type 1 cells. The mutant GlcCer-beta-glucosidase from our studied type 2 lymphoid cells was profoundly labile at pH 4.0 and 37 degrees C, whereas the residual GlcCer-beta-glucosidase from type 1 and type 3 were stable similar to the normal enzyme. In contrast to the distinct stability of the GlcCer-beta-glucosidases from the three phenotypes, the acid lability of the nonspecific membrane-bound beta-glucosidases from type 1, 2 and 3 were quite similar.</p>","PeriodicalId":11933,"journal":{"name":"Enzyme","volume":"43 2","pages":"99-106"},"PeriodicalIF":0.0,"publicationDate":"1990-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1159/000468712","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"13279092","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 1
Selective translation and degradation of heat-shock messenger RNAs in Drosophila. 果蝇热休克信使rna的选择性翻译和降解。
Enzyme Pub Date : 1990-01-01 DOI: 10.1159/000468754
S Lindquist, R Petersen
{"title":"Selective translation and degradation of heat-shock messenger RNAs in Drosophila.","authors":"S Lindquist,&nbsp;R Petersen","doi":"10.1159/000468754","DOIUrl":"https://doi.org/10.1159/000468754","url":null,"abstract":"<p><p>The rapid and dramatic induction of heat-shock proteins is accomplished by regulatory mechanisms acting at many different levels. Here we review current knowledge of two cytoplasmic mechanisms employed during the response in the fruit fly Drosophila melanogaster. (1) Heat-shock messages are translated with high efficiency during heat shock while most normal cellular messages are inactive. Sequences in the 5'-untranslated leader of heat shock mRNAs govern their preferential translation. (2) The messages for heat-shock proteins are unstable at normal temperatures. During heat shock, however, they are very stable and accumulate in large numbers. Sequences in their 3'-untranslated regions play a major role in determining their stability.</p>","PeriodicalId":11933,"journal":{"name":"Enzyme","volume":"44 1-4","pages":"147-66"},"PeriodicalIF":0.0,"publicationDate":"1990-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1159/000468754","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"13288330","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 84
Enzymatic activities related to intermediary metabolism of glucose in circulating mononuclear cells from obese humans: relationship to enzyme activity in adipose tissue. 肥胖人群循环单核细胞中与葡萄糖中间代谢相关的酶活性:与脂肪组织中酶活性的关系。
Enzyme Pub Date : 1990-01-01 DOI: 10.1159/000468702
P Moghetti, E Bonora, M Cigolini, M Querena, V Cacciatori, M Muggeo
{"title":"Enzymatic activities related to intermediary metabolism of glucose in circulating mononuclear cells from obese humans: relationship to enzyme activity in adipose tissue.","authors":"P Moghetti,&nbsp;E Bonora,&nbsp;M Cigolini,&nbsp;M Querena,&nbsp;V Cacciatori,&nbsp;M Muggeo","doi":"10.1159/000468702","DOIUrl":"https://doi.org/10.1159/000468702","url":null,"abstract":"<p><p>In order to assess whether enzyme activities of glucose metabolism measured in mononuclear blood cells reflect those in a typical insulin target tissue, we studied hexokinase, 6-phosphofructokinase, glucose-6-phosphate dehydrogenase, and 6-phosphogluconate dehydrogenase activities in lymphomonocytes and in hypogastric adipose tissue from 15 nondiabetic obese women. Statistically significant relationships were found in the activities of hexokinase (r = 0.53, p less than 0.05), 6-phosphofructokinase (r = 0.85, p less than 0.01), and 6-phosphogluconate dehydrogenase (r = 0.72, p less than 0.01) between the two tissues. These results suggest that mononuclear blood cells may be suitable as a model for studying cytosolic key enzymes involved in the glucose metabolism of humans.</p>","PeriodicalId":11933,"journal":{"name":"Enzyme","volume":"43 1","pages":"26-32"},"PeriodicalIF":0.0,"publicationDate":"1990-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1159/000468702","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"13295948","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 4
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