Comparative Biochemistry and Physiology Part B: Comparative Biochemistry最新文献

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Isolation and characterization of a 21 kDa whey protein in Rhesus monkey (Macaca mulatta) milk 恒河猴(Macaca mulatta)牛奶中21 kDa乳清蛋白的分离与鉴定
Comparative Biochemistry and Physiology Part B: Comparative Biochemistry Pub Date : 1994-08-01 DOI: 10.1016/0305-0491(94)90099-X
Clemens Kunz , Bo Lönnerdal
{"title":"Isolation and characterization of a 21 kDa whey protein in Rhesus monkey (Macaca mulatta) milk","authors":"Clemens Kunz ,&nbsp;Bo Lönnerdal","doi":"10.1016/0305-0491(94)90099-X","DOIUrl":"10.1016/0305-0491(94)90099-X","url":null,"abstract":"<div><p>A soluble protein in Rhesus monkey milk was isolated to apparent homogeneity by FPLC gel filtration, anion-exchange and reverse-phase chromatography. It is a major milk protein and is present at 2.5—3.0 mg/ml milk throughout lactation. It is only found in the whey fraction of milk; acid precipitation of casein does not result in any significant change in its concentration. A molecular weight (MW) of about 21.6 kDa was estimated from gel filtration and SDS gel electrophoresis and also calculated from its amino acid composition. The amino acid composition of this protein is similar to that of bovine β-lactoglobulin (β-Lg), but it is larger in size, possibly representing a family of primate β-Lgs.</p></div>","PeriodicalId":100294,"journal":{"name":"Comparative Biochemistry and Physiology Part B: Comparative Biochemistry","volume":"108 4","pages":"Pages 463-469"},"PeriodicalIF":0.0,"publicationDate":"1994-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/0305-0491(94)90099-X","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"18947160","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: 11
A decrease of free radical production near critical targets as a cause of maximum longevity in animals 自由基减少:动物在关键目标附近自由基产生的减少,是最大寿命的原因
Comparative Biochemistry and Physiology Part B: Comparative Biochemistry Pub Date : 1994-08-01 DOI: 10.1016/0305-0491(94)90103-1
G. Barja, S. Cadenas, C. Rojas, M. López-Torres, R. Pèrez-Campo
{"title":"A decrease of free radical production near critical targets as a cause of maximum longevity in animals","authors":"G. Barja,&nbsp;S. Cadenas,&nbsp;C. Rojas,&nbsp;M. López-Torres,&nbsp;R. Pèrez-Campo","doi":"10.1016/0305-0491(94)90103-1","DOIUrl":"10.1016/0305-0491(94)90103-1","url":null,"abstract":"<div><p>A comprehensive study was performed on the brains of various vertebrate species showing different life energy potentials in order to find out if free radicals are important determinants of species-specific maximum life span. Brain superoxide dismutase, catalase, Se-dependent and independent GSH-peroxidases, GSH-reductase, and ascorbic acid showed significant inverse correlations with maximum longevity, whereas GSH, uric acid, GSSG/GSH, <em>in vitro</em> peroxidation (thiobarbituric acid test), and malondialdehyde (measured by HPLC), did not correlate with maximum life span. Superoxide dismutase, catalase, GSH-peroxidase, GSH and ascorbate results agree with those previously reported in various independent works using different animal species. GSSG/GSH, and true malondialdehyde (HPLC) results are reported for the first time in relation to maximum longevity. The results suggest that longevous species simultaneously show low antioxidant concentrations and low levels of <em>in vivo</em> free radical production (a low free radical turnover) in their tissues. The “free radical production hypothesis of aging” is proposed: a decrease in oxygen radical production per unit of O<sub>2</sub> consumption <em>near critical DNA targets</em> (mitochondria or nucleus) increases the maximum life span of extraordinarily long-lived species like birds, primates, and man. Free radical production near these DNA sites would be a main factor responsible for aging in all the species, in those following Pearl's (Rubner's) metabolic rule as well as in those not following it.</p></div>","PeriodicalId":100294,"journal":{"name":"Comparative Biochemistry and Physiology Part B: Comparative Biochemistry","volume":"108 4","pages":"Pages 501-512"},"PeriodicalIF":0.0,"publicationDate":"1994-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/0305-0491(94)90103-1","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"18947163","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: 109
Patterns of lactate and sorbitol dehydrogenase gene expression during the development of interspecific Rasbora hybrids 种间杂交种发育过程中乳酸脱氢酶和山梨糖醇脱氢酶基因的表达模式
Comparative Biochemistry and Physiology Part B: Comparative Biochemistry Pub Date : 1994-08-01 DOI: 10.1016/0305-0491(94)90096-5
Jack S. Frankel
{"title":"Patterns of lactate and sorbitol dehydrogenase gene expression during the development of interspecific Rasbora hybrids","authors":"Jack S. Frankel","doi":"10.1016/0305-0491(94)90096-5","DOIUrl":"10.1016/0305-0491(94)90096-5","url":null,"abstract":"<div><p>The expression of alleles encoding the enzymes lactate dehydrogenase (LDH; EC 1.1.1.27) and sorbitol dehydrogenase (SDH; EC 1.1.1.14) was investigated in the redtail rasbora (<em>Rasbora borapetensis</em>), the eyespot rasbora (<em>R. dorsiocellata</em>), and in their reciprocal hybrids, by acrylamide gel electrophoresis. The spatial and temporal expression of LDH and SDH isozymes in <em>Rasbora</em> is consistent with those reported for other teleosts. The asynchronous delay in appearance of isozymes of paternal and maternal LDH-C and SDH-A subunit composition is in keeping with observed effects of gene regulatory divergence where alleles of maternal origin interact more effectively with maternal cytoplasmic regulatory factors than do alleles of paternal origin.</p></div>","PeriodicalId":100294,"journal":{"name":"Comparative Biochemistry and Physiology Part B: Comparative Biochemistry","volume":"108 4","pages":"Pages 437-441"},"PeriodicalIF":0.0,"publicationDate":"1994-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/0305-0491(94)90096-5","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"85447491","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
Prolactin gene expression and changes of prolactin pituitary level during the seasonal acclimatization of the carp 鲤季节性适应过程中催乳素基因表达及垂体催乳素水平的变化
Comparative Biochemistry and Physiology Part B: Comparative Biochemistry Pub Date : 1994-08-01 DOI: 10.1016/0305-0491(94)90109-0
Jaime Figueroa, Alfredo Molina, Marco Alvarez, Julieta Villanueva, Ariel Reyes, Gloria León, Manuel Krauskopf
{"title":"Prolactin gene expression and changes of prolactin pituitary level during the seasonal acclimatization of the carp","authors":"Jaime Figueroa,&nbsp;Alfredo Molina,&nbsp;Marco Alvarez,&nbsp;Julieta Villanueva,&nbsp;Ariel Reyes,&nbsp;Gloria León,&nbsp;Manuel Krauskopf","doi":"10.1016/0305-0491(94)90109-0","DOIUrl":"10.1016/0305-0491(94)90109-0","url":null,"abstract":"<div><p>The effect of seasonal acclimatization on the extent of prolactin (PRL) gene expression and on the content of this was studied in summer- and winter-carp (<em>Cyprinus carpio</em>) hormone pituitary glands. PRL content in the rostral pars distalis (RPD) was evaluated by immunocytochemistry using antibodies against a cross-linked synthetic peptide comprising the sequence of 15 amino acids which conform to the primary structure of carp PRL. To assess the level of PRL gene transcription, a 24-mer synthetic oligonucleotide probe whose sequence included nucleotides 2041–2064 located in exon V of the carp PRL gene, was used. Employing <em>in situ</em> hybridization assays, a high expression of PRL mRNA was observed in the RPD of summer-acclimatized carp. A negligible level of transcription was observed in tissue sections of pituitary glands from winter-acclimatized carp. Concurrently, immunodetection of the PRL-producing cells in the RPD revealed that the pituitary hormone level was significantly higher in the warm season-adapted carp.</p></div>","PeriodicalId":100294,"journal":{"name":"Comparative Biochemistry and Physiology Part B: Comparative Biochemistry","volume":"108 4","pages":"Pages 551-560"},"PeriodicalIF":0.0,"publicationDate":"1994-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/0305-0491(94)90109-0","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"18952361","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: 28
Lactate dehydrogenase, alanopine dehydrogenase and octopine dehydrogenase from the heart of Concholepas concholepas (Gastropoda: Muricidae) 腹足目:蠓科(腹足目:蠓科)心乳酸脱氢酶、丙氨酸脱氢酶和章鱼碱脱氢酶
Comparative Biochemistry and Physiology Part B: Comparative Biochemistry Pub Date : 1994-08-01 DOI: 10.1016/0305-0491(94)90108-2
Nelson Carvajal, Edgardo Vega, Alejandro Erices, Daniel Bustos, Claudio Torres
{"title":"Lactate dehydrogenase, alanopine dehydrogenase and octopine dehydrogenase from the heart of Concholepas concholepas (Gastropoda: Muricidae)","authors":"Nelson Carvajal,&nbsp;Edgardo Vega,&nbsp;Alejandro Erices,&nbsp;Daniel Bustos,&nbsp;Claudio Torres","doi":"10.1016/0305-0491(94)90108-2","DOIUrl":"10.1016/0305-0491(94)90108-2","url":null,"abstract":"<div><p>Alanopine dehydrogenase, octopine dehydrogenase and lactate dehydrogenase activities were detected in the heart of <em>C. concholepas</em>. As determined by gel filtration on Sephadex G-100, the molecular weights (<em>M</em><sub>r</sub>) were 85,000, 42,000 and 52,000 for lactate dehydrogenase, alanopine dehydrogenase and octopine dehydrogenase, respectively. Substrate inhibition of the opine dehydrogenases was observed at high concentrations of both pyruvate and the corresponding amino acid (alanine or arginine). Moderate substrate inhibition of lactate dehydrogenase by pyruvate was observed; <em>K</em><sub>m</sub> values for lactate and NAD<sup>+</sup> were unusually high. Alanoonine dehydrogenase was very specific for alanine and glycine was not a substrate for this enzyme. In addition to arginine, lysine was also a substrate for octopine dehydrogenase. Possible functions of the pyruvate reductases are discussed in connection with adaptation to anoxia and other regulatory processes in the heart of <em>C. concholepas</em>.</p></div>","PeriodicalId":100294,"journal":{"name":"Comparative Biochemistry and Physiology Part B: Comparative Biochemistry","volume":"108 4","pages":"Pages 543-550"},"PeriodicalIF":0.0,"publicationDate":"1994-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/0305-0491(94)90108-2","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"75116780","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
Polysome profiles in awake and estivating snails (Otala lactea) 醒蜗牛和活动蜗牛的多体分布
Comparative Biochemistry and Physiology Part B: Comparative Biochemistry Pub Date : 1994-08-01 DOI: 10.1016/0305-0491(94)90095-7
Andrew A. Hobbs, Janet M. Attwood, Michael Guppy
{"title":"Polysome profiles in awake and estivating snails (Otala lactea)","authors":"Andrew A. Hobbs,&nbsp;Janet M. Attwood,&nbsp;Michael Guppy","doi":"10.1016/0305-0491(94)90095-7","DOIUrl":"10.1016/0305-0491(94)90095-7","url":null,"abstract":"<div><p>The land snail, <em>Otala lactea</em>, like many other organisms, depresses its metabolism in the face of environmental stress. Due to the extent of this depression, a decrease in the rate of protein synthesis is likely to be involved. In an attempt to quantitate changes in the rate of protein synthesis during metabolic depression in <em>O. lactea</em> we have determined polysome profiles from the hepatopancreas of awake and estivating snails. In both estivating and awake snails, the majority of ribosomes were present as monosomes and there was no evidence of qualitative changes with the state of the snail.</p></div>","PeriodicalId":100294,"journal":{"name":"Comparative Biochemistry and Physiology Part B: Comparative Biochemistry","volume":"108 4","pages":"Pages 431-436"},"PeriodicalIF":0.0,"publicationDate":"1994-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/0305-0491(94)90095-7","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"75793885","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: 6
Purification and characterization of multifunctional enzyme from mouse liver peroxisomes 小鼠肝脏过氧化物酶体多功能酶的纯化及特性研究
Comparative Biochemistry and Physiology Part B: Comparative Biochemistry Pub Date : 1994-08-01 DOI: 10.1016/0305-0491(94)90100-7
Annika Stark, Johan Meijer
{"title":"Purification and characterization of multifunctional enzyme from mouse liver peroxisomes","authors":"Annika Stark,&nbsp;Johan Meijer","doi":"10.1016/0305-0491(94)90100-7","DOIUrl":"10.1016/0305-0491(94)90100-7","url":null,"abstract":"<div><p>A simple and rapid purification procedure for hepatic peroxisomal multifunctional enzyme (Δ<sup>3</sup>,Δ<sup>2</sup>-enoyl-CoA isomerase/enoyl-CoA hydratase/3-hydroxyacyl-CoA dehydrogenase) from clofibrate treated mice is described. The purification is achieved within two days using ion-exchange chromatography and an easily prepared affinity resin. The overall yield is 10% or more after a 100-fold enrichment from the cytosolic fraction of liver tissue. The native enzyme is a monomer with a molecular mass of 75 kDa. The protein is blocked in the <em>N</em>-terminus but internal amino acid sequences was obtained after proteolytic cleavage. Western blot analysis indicated proteolysis of multifunctional enzyme in different subcellular fractions derived from liver tissue. The hydratase activity of the enzyme is heat-labile and highly dependent on the concentration of Tris buffer or potassium chloride present. Optimal activity was found around 37°C and pH 7. The enzyme also shows dehydrogenase and isomerase activity.</p></div>","PeriodicalId":100294,"journal":{"name":"Comparative Biochemistry and Physiology Part B: Comparative Biochemistry","volume":"108 4","pages":"Pages 471-480"},"PeriodicalIF":0.0,"publicationDate":"1994-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/0305-0491(94)90100-7","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"18947161","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: 3
2-Methylbutyryl-CoA: succinate acyl-CoA transferase activity and function in Ascaris suum muscle 2-甲基丁基辅酶a:琥珀酸酰基辅酶a转移酶在猪蛔虫肌肉中的活性和功能
Comparative Biochemistry and Physiology Part B: Comparative Biochemistry Pub Date : 1994-08-01 DOI: 10.1016/0305-0491(94)90104-X
Howard J. Saz, Becky S. deBruyn
{"title":"2-Methylbutyryl-CoA: succinate acyl-CoA transferase activity and function in Ascaris suum muscle","authors":"Howard J. Saz,&nbsp;Becky S. deBruyn","doi":"10.1016/0305-0491(94)90104-X","DOIUrl":"10.1016/0305-0491(94)90104-X","url":null,"abstract":"<div><p>A branched-chain acyl-CoA transferase activity which transfers coenzyme A from either 2-methylbutyryl or 2-methylvaleryl-CoA to succinate is present in the muscle mitochondria from the intestinal nematode, <em>Ascaris suum</em>. Its physiological function is discussed. This activity appears to differ from the previously described acetyl-CoA:propionate and propionyl-CoA:succinate acyl-CoA transferases on the basis of heat stability, substrate specificity and the requirement of a “factor” from boiled <em>Ascaris</em> mitochondria for optimal activity of only the branched-chain acyl-CoA transferase. The “factor” has been recovered from HPLC and some of its properties examined. It could not be replaced by a crude soluble fraction from rat liver mitochondria, or by adenine, guanine or inosine di- or triphosphates. Activity was lost upon ashing, but was not affected by treatment with either pepsin or chymotrypsin.</p></div>","PeriodicalId":100294,"journal":{"name":"Comparative Biochemistry and Physiology Part B: Comparative Biochemistry","volume":"108 4","pages":"Pages 513-519"},"PeriodicalIF":0.0,"publicationDate":"1994-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/0305-0491(94)90104-X","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"18947164","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
Comparative study of the endemic freshwater fauna of Lake Baikal—V. Phospholipid and fatty acid composition of the deep-water amphipod crustacean Acanthogammarus (Brachyuropus) grewingkii 贝加尔湖特有淡水动物群的比较研究。深海片脚甲壳类棘鱼(Acanthogammarus)磷脂和脂肪酸组成
Comparative Biochemistry and Physiology Part B: Comparative Biochemistry Pub Date : 1994-08-01 DOI: 10.1016/0305-0491(94)90097-3
Valery M. Dembitsky , Andrey G. Kashin , Tomas Rezanka
{"title":"Comparative study of the endemic freshwater fauna of Lake Baikal—V. Phospholipid and fatty acid composition of the deep-water amphipod crustacean Acanthogammarus (Brachyuropus) grewingkii","authors":"Valery M. Dembitsky ,&nbsp;Andrey G. Kashin ,&nbsp;Tomas Rezanka","doi":"10.1016/0305-0491(94)90097-3","DOIUrl":"10.1016/0305-0491(94)90097-3","url":null,"abstract":"<div><p>Lipid and phospholipid compositions of an endemic deep-water freshwater gammarid, belonging to the subphylum Crustacea, <em>Acanthogammarus grewingkii</em> was studied. Content of alkenylacyl, alkylacyl and diacyl forms in the main phospholipid classes (phosphatidylethanolamine and phosphatydilcholine) were established using reaction micro-thin-layer chromatography. The fatty acids compositions of total lipids, neutral, glyco- and phospholipid fractions were investigated by capillary gas chromatography-mass spectrometry. Seventy-nine fatty acids were identified: 26 saturated (iso-, anteiso- and cyclo-), 26 monoenoic, 7 dienoic, 14 trienoic and 16 tetra-, penta- and hexaenoic. A number of demospongic fatty acids, such as 5,9–25:2, 5,9,19–26:3, 5,9,17–26:3, 5,9,23–28:3 and 5,9,21–28:3 acids, were found.</p></div>","PeriodicalId":100294,"journal":{"name":"Comparative Biochemistry and Physiology Part B: Comparative Biochemistry","volume":"108 4","pages":"Pages 443-448"},"PeriodicalIF":0.0,"publicationDate":"1994-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/0305-0491(94)90097-3","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"82949086","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: 15
Comparative biochemistry and physiology B bibliography 比较生物化学与生理学B参考书目
Comparative Biochemistry and Physiology Part B: Comparative Biochemistry Pub Date : 1994-08-01 DOI: 10.1016/0305-0491(94)90112-0
{"title":"Comparative biochemistry and physiology B bibliography","authors":"","doi":"10.1016/0305-0491(94)90112-0","DOIUrl":"https://doi.org/10.1016/0305-0491(94)90112-0","url":null,"abstract":"","PeriodicalId":100294,"journal":{"name":"Comparative Biochemistry and Physiology Part B: Comparative Biochemistry","volume":"108 4","pages":"Pages i-iii"},"PeriodicalIF":0.0,"publicationDate":"1994-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/0305-0491(94)90112-0","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"137161410","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
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