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

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Antibacterial protection in Marthasterias glacialis eggs: characterization of lysozyme-like activity 冰马氏菌卵的抗菌保护作用:溶菌酶样活性的表征
Comparative Biochemistry and Physiology Part B: Comparative Biochemistry Pub Date : 1994-12-01 DOI: 10.1016/0305-0491(94)90134-1
L. Stabili, P. Pagliara
{"title":"Antibacterial protection in Marthasterias glacialis eggs: characterization of lysozyme-like activity","authors":"L. Stabili,&nbsp;P. Pagliara","doi":"10.1016/0305-0491(94)90134-1","DOIUrl":"10.1016/0305-0491(94)90134-1","url":null,"abstract":"<div><p>Eggs from <em>Marthastherias glacialis</em> exert antibacterial action on marine bacterial strains and show a lysozyme-like activity. This one depends on pH and ionic strength of sample and reacting medium. This hydrolase, purified by gel filtration and ion-exchange chromatography, could be responsible for the bacterial growth inhibitory activity observed.</p></div>","PeriodicalId":100294,"journal":{"name":"Comparative Biochemistry and Physiology Part B: Comparative Biochemistry","volume":"109 4","pages":"Pages 709-713"},"PeriodicalIF":0.0,"publicationDate":"1994-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/0305-0491(94)90134-1","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"18879981","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: 26
Glutamine and glucose metabolism in intraepithelial lymphocytes from pre- and post-weaning pigs 断奶前后仔猪上皮内淋巴细胞的谷氨酰胺和葡萄糖代谢
Comparative Biochemistry and Physiology Part B: Comparative Biochemistry Pub Date : 1994-12-01 DOI: 10.1016/0305-0491(94)90130-9
M.E.R. Dugan, D.A. Knabe, G. Wu
{"title":"Glutamine and glucose metabolism in intraepithelial lymphocytes from pre- and post-weaning pigs","authors":"M.E.R. Dugan,&nbsp;D.A. Knabe,&nbsp;G. Wu","doi":"10.1016/0305-0491(94)90130-9","DOIUrl":"10.1016/0305-0491(94)90130-9","url":null,"abstract":"<div><p>The metabolism of glutamine (Gln) and glucose was studied in intraepithelial lymphocytes (IEL) from 21-, 29- and 56-day-old pigs. Pigs were weaned at 21 days of age. Cells were incubated at 37°C in the presence of Krebs-Ringer bicarbonate buffer (pH 7.4) containing 1 mM [U<sup>14</sup>C]glutamine plus 5 mM glucose, or 5 mM [U<sup>14</sup>C]glucose plus 1 mM glutamine. Glucose was converted to lactate, pyruvate and CO<sub>2</sub>, which accounted for 81, 11 and 8% of measured glucose carbon, respectively. Glutamine was metabolized mainly to glutamate (92% of Gln C) and ammonia, and to a lesser extent, to aspartate (4% of Gln C) and CO<sub>2</sub> (4% of Gln C). In the presence of both glucose and glutamine, glucose provided 2–3-fold more ATP to IELs than glutamine in 21–56-day-old pigs, on the basis of their measured end products. The rates of ammonia and glutamate production from glutamine in IELs from 29-day-old pigs were 112 and 90% greater than those in cells from 56-day-old pigs, respectively. The rates of glucose oxidation to CO<sub>2</sub> in IELs from 29-day-old pigs were elevated 56 and 64% respectively, compared with 21- and 56-day-old pigs. Elevated rates of substrate metabolism in IELs from 29-day-old post-weaning pigs indicated a metabolic alteration of these cells possibly due to changes in diet and intestinal bacterial population.</p></div>","PeriodicalId":100294,"journal":{"name":"Comparative Biochemistry and Physiology Part B: Comparative Biochemistry","volume":"109 4","pages":"Pages 675-681"},"PeriodicalIF":0.0,"publicationDate":"1994-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/0305-0491(94)90130-9","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"18879980","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: 25
Purification and establishment of ELISA for vitellogenin of Japanese sardine (Sardinops melanostictus) 日本沙丁鱼(Sardinops melanotictus)卵黄蛋白原酶联免疫吸附试验的纯化与建立
Comparative Biochemistry and Physiology Part B: Comparative Biochemistry Pub Date : 1994-12-01 DOI: 10.1016/0305-0491(94)90116-3
Takahiro Matsubara , Tokio Wada , Akihiko Hara
{"title":"Purification and establishment of ELISA for vitellogenin of Japanese sardine (Sardinops melanostictus)","authors":"Takahiro Matsubara ,&nbsp;Tokio Wada ,&nbsp;Akihiko Hara","doi":"10.1016/0305-0491(94)90116-3","DOIUrl":"10.1016/0305-0491(94)90116-3","url":null,"abstract":"<div><p>Two female-specific serum proteins (FSSPs) were detected immunologically in estradiol-treated Japanese sardine <em>Sardinops melanostictus</em>. The major FSSP was demonstrated to be a high molecular estradiol-inducible glycolipophosphoprotein with an immunological relation to a major yolk protein, and was suggested to be vitellogenin (VTG). VTG was purified using negative immunoaffinity chromatography. The isolated VTG was used for raising the specific antiserum against VTG. A homologous enzyme-linked immunosorbent assay (ELISA) was developed using the antiserum and the isolated VTG. The sensitivity range of the ELISA was 44 ng/ml to 2670 ng/ml of VTG concentration for the conditions used in our investigation.</p></div>","PeriodicalId":100294,"journal":{"name":"Comparative Biochemistry and Physiology Part B: Comparative Biochemistry","volume":"109 4","pages":"Pages 545-555"},"PeriodicalIF":0.0,"publicationDate":"1994-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/0305-0491(94)90116-3","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"85693128","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: 27
NAD-dependent glutamate dehydrogenase from the thermophilic eubacterium Bacillus acidocaldarius 嗜热嗜酸芽孢杆菌的nadd依赖性谷氨酸脱氢酶
Comparative Biochemistry and Physiology Part B: Comparative Biochemistry Pub Date : 1994-12-01 DOI: 10.1016/0305-0491(94)90132-5
Valerio Consalvi , Roberta Chiaraluce , Stefania Millevoi , Alessandra Pasquo , Laura Politi , Mario De Rosa , Roberto Scandurra
{"title":"NAD-dependent glutamate dehydrogenase from the thermophilic eubacterium Bacillus acidocaldarius","authors":"Valerio Consalvi ,&nbsp;Roberta Chiaraluce ,&nbsp;Stefania Millevoi ,&nbsp;Alessandra Pasquo ,&nbsp;Laura Politi ,&nbsp;Mario De Rosa ,&nbsp;Roberto Scandurra","doi":"10.1016/0305-0491(94)90132-5","DOIUrl":"10.1016/0305-0491(94)90132-5","url":null,"abstract":"<div><p>The first thermophilic eubacterial glutamate dehydrogenase was purified to homogeneity from <em>Bacillus acidocaldarius</em> to compare its molecular properties with those of the glutamate dehydrogenase from thermophilic archaea. Glutamate dehydrogenase represents 2% of the total soluble proteins of <em>B. acidocaldarius</em>, an amount that may suggest an important role for this enzyme in nitrogen metabolism of the thermophilic eubacterium. The protein is a hexamer (subunit mass 48 kDa) and undergoes dissociation during gel filtration analysis. Isoelectric focusing of the purified enzyme indicated a pI of 4.5. The enzyme is strictly specific for NAD, 2-oxoglutarate, and <span>l</span>-glutamate. The thermal stability of <em>B. acidocaldarius</em> glutamate dehydrogenase is dependent on protein concentration.</p></div>","PeriodicalId":100294,"journal":{"name":"Comparative Biochemistry and Physiology Part B: Comparative Biochemistry","volume":"109 4","pages":"Pages 691-699"},"PeriodicalIF":0.0,"publicationDate":"1994-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/0305-0491(94)90132-5","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"82459582","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
Volume contents, subject and author index volume 109 partB, 1994 卷的内容、主题和作者索引,第109卷b部分,1994年
Comparative Biochemistry and Physiology Part B: Comparative Biochemistry Pub Date : 1994-12-01 DOI: 10.1016/0305-0491(94)90139-2
{"title":"Volume contents, subject and author index volume 109 partB, 1994","authors":"","doi":"10.1016/0305-0491(94)90139-2","DOIUrl":"https://doi.org/10.1016/0305-0491(94)90139-2","url":null,"abstract":"","PeriodicalId":100294,"journal":{"name":"Comparative Biochemistry and Physiology Part B: Comparative Biochemistry","volume":"109 4","pages":"Pages I-XIV"},"PeriodicalIF":0.0,"publicationDate":"1994-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/0305-0491(94)90139-2","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"137439705","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
Purification, characterization and amino terminal sequence of the superoxide dismutase from Babesia hylomysci 巴贝斯虫超氧化物歧化酶的纯化、鉴定及氨基末端序列分析
Comparative Biochemistry and Physiology Part B: Comparative Biochemistry Pub Date : 1994-12-01 DOI: 10.1016/0305-0491(94)90126-0
P. Becuwe , J. van Beeumen , B. Samyn , J.P. Touzel , C. Slomianny , D. Camus , D. Dive
{"title":"Purification, characterization and amino terminal sequence of the superoxide dismutase from Babesia hylomysci","authors":"P. Becuwe ,&nbsp;J. van Beeumen ,&nbsp;B. Samyn ,&nbsp;J.P. Touzel ,&nbsp;C. Slomianny ,&nbsp;D. Camus ,&nbsp;D. Dive","doi":"10.1016/0305-0491(94)90126-0","DOIUrl":"10.1016/0305-0491(94)90126-0","url":null,"abstract":"<div><p><em>Babesia hylomysci</em> was found to contain two superoxide dismutase (SOD) isoenzymes with isoelectric points (p<em>I</em>) of 4.9 and 5.2. The two isoenzymes (45 and 47 kDa) were composed of two subunits of 22 kDa. An unique amino terminal sequence was determined up to 34 residues from the pooled isoenzymes and was identified as a sequence of SOD. The comparison of this <em>N</em>-terminal sequence of <em>B. hylomysci</em> SOD with 29 known Fe- or Mn-SODs showed more homologies with Fe-SODs.</p></div>","PeriodicalId":100294,"journal":{"name":"Comparative Biochemistry and Physiology Part B: Comparative Biochemistry","volume":"109 4","pages":"Pages 637-645"},"PeriodicalIF":0.0,"publicationDate":"1994-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/0305-0491(94)90126-0","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"18881981","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: 5
Demonstration and preliminary characterization of α-amylase in the sweetpotato whitefly, Bemisia tabaci (Aleyrodidae: Homoptera) 甘薯粉虱α-淀粉酶的鉴定与初步鉴定(粉虱科:同翅目)
Comparative Biochemistry and Physiology Part B: Comparative Biochemistry Pub Date : 1994-12-01 DOI: 10.1016/0305-0491(94)90122-8
Allen Carson Cohen, Donald L. Hendrix
{"title":"Demonstration and preliminary characterization of α-amylase in the sweetpotato whitefly, Bemisia tabaci (Aleyrodidae: Homoptera)","authors":"Allen Carson Cohen,&nbsp;Donald L. Hendrix","doi":"10.1016/0305-0491(94)90122-8","DOIUrl":"10.1016/0305-0491(94)90122-8","url":null,"abstract":"<div><p>An α-amylase that hydrolyzes unmodified starch or amylopectin azure was demonstrated in crude and partially purified extracts prepared from whole carcasses of sweetpotato whiteflies (SPW) (<em>Bemisia tabaci</em> Genn.).</p><p>All nymphal instars and adult SPW, including newly eclosed crawlers that had not yet fed on plant materials, were found to have active α-amylase. α-Amylase activity per mg protein was greatest in 1st instars and decreased with age up to the “pupal” stage, with a very slight increase in activity in adults. However, activity per individual did not differ substantially as a function of age.</p><p>The α-amylase had an apparent molecular weight of about 70 kDa, an isoelectric point of 6.32 and eluted with about 250 mM NaCl from a strongly basic anion-exchange column.</p><p>The enzyme activity was inhibited by EDTA and not activated by either NaCl or KNO<sub>3</sub>. CaCl<sub>2</sub> strongly enhanced activity.</p><p>α-Amylase activity was greatest at pH 7.0, but there was considerable activity at pHs above 7.0.</p><p>The <em>K</em><sub>m</sub> of the α-amylase was 1.47 Mm with <em>p</em>-nitrophenyl α-<span>d</span>-malto-heptaoside as substrate.</p><p>The presence of an amylolytic enzyme in a phloem-feeding insect is unexpected and raises questions about current assumptions of feeding behavior of this species.</p></div>","PeriodicalId":100294,"journal":{"name":"Comparative Biochemistry and Physiology Part B: Comparative Biochemistry","volume":"109 4","pages":"Pages 593-601"},"PeriodicalIF":0.0,"publicationDate":"1994-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/0305-0491(94)90122-8","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"91296388","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: 22
Glutathione S-transferases from the gastrointestinal nematode Heligmosomoides polygyrus and mammalian liver compared 胃肠道线虫和哺乳动物肝脏中谷胱甘肽s转移酶的比较
Comparative Biochemistry and Physiology Part B: Comparative Biochemistry Pub Date : 1994-12-01 DOI: 10.1016/0305-0491(94)90121-X
Peter M. Brophy , Anne Ben-Smith , Alan Brown , Jerzy M. Behnke , David I. Pritchard
{"title":"Glutathione S-transferases from the gastrointestinal nematode Heligmosomoides polygyrus and mammalian liver compared","authors":"Peter M. Brophy ,&nbsp;Anne Ben-Smith ,&nbsp;Alan Brown ,&nbsp;Jerzy M. Behnke ,&nbsp;David I. Pritchard","doi":"10.1016/0305-0491(94)90121-X","DOIUrl":"10.1016/0305-0491(94)90121-X","url":null,"abstract":"<div><p>Glutathione <em>S</em>-transferases have been partially characterised from the gastrointestinal nematode <em>Heligmosomoides polygyrus</em>. Two major subunit families were purified (24 and 23 kDa) with <em>N</em>-terminal homology to the mammalian Alpha family. Four dimeric forms of GST were purified from the nematode by glutathione-affinity chromatography, two major enzymes (pI 8.1, 5.0) and two minor forms (pI 5.8, 5.3). The purified GST pool could neutralize model and lipid peroxides via peroxidase activity but not peroxidation derived reactive carbonyls via glutathione transferase activity. Antisera raised to the pooled nematode GSTs appeared to recognize other Strongylida GSTs more strongly on Western blotting compared to mammalian GSTs.</p></div>","PeriodicalId":100294,"journal":{"name":"Comparative Biochemistry and Physiology Part B: Comparative Biochemistry","volume":"109 4","pages":"Pages 585-592"},"PeriodicalIF":0.0,"publicationDate":"1994-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/0305-0491(94)90121-X","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"18881978","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
Relationship between the induction of proteins in the HSP70 family and thermosensitivity in two species of Oryzias (Pisces) 两种稻属植物HSP70家族蛋白诱导与热敏性的关系
Comparative Biochemistry and Physiology Part B: Comparative Biochemistry Pub Date : 1994-12-01 DOI: 10.1016/0305-0491(94)90127-9
Ayami Arai, Hiroshi Mitani, Kiyoshi Naruse, Akihiro Shima
{"title":"Relationship between the induction of proteins in the HSP70 family and thermosensitivity in two species of Oryzias (Pisces)","authors":"Ayami Arai,&nbsp;Hiroshi Mitani,&nbsp;Kiyoshi Naruse,&nbsp;Akihiro Shima","doi":"10.1016/0305-0491(94)90127-9","DOIUrl":"10.1016/0305-0491(94)90127-9","url":null,"abstract":"<div><p>A cultured fish cell line, CE, derived from <em>Oryzias celebensis</em>, which lives in a tropical zone, was more heat-resistant than the OL32, which were derived from the Japanese medaka, <em>Oryzias latipes</em> which lives in a temperate zone. Protein synthesis in OL32 cells was also more heat-sensitive than that in CE cells. The relative levels in proteins of the HSP70 family and the ability of cells to tolerate severe heat treatment after a conditioning heat treatment were examined. Twenty-four hours after conditioning heat treatment, both cell lines retained thermotolerance even though three proteins in the HSP70 family had returned to their control levels.</p></div>","PeriodicalId":100294,"journal":{"name":"Comparative Biochemistry and Physiology Part B: Comparative Biochemistry","volume":"109 4","pages":"Pages 647-654"},"PeriodicalIF":0.0,"publicationDate":"1994-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/0305-0491(94)90127-9","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"18881982","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: 23
In vitro biosynthesis of steroids in ovary of asynchronic Trichogaster trichopterus (Pallus, 1770) 非慢性trichoaster trichopterus卵巢内类固醇的体外生物合成(Pallus, 1770)
Comparative Biochemistry and Physiology Part B: Comparative Biochemistry Pub Date : 1994-12-01 DOI: 10.1016/0305-0491(94)90135-X
Gad Degani , Erez Gal , Jacob Vaya
{"title":"In vitro biosynthesis of steroids in ovary of asynchronic Trichogaster trichopterus (Pallus, 1770)","authors":"Gad Degani ,&nbsp;Erez Gal ,&nbsp;Jacob Vaya","doi":"10.1016/0305-0491(94)90135-X","DOIUrl":"10.1016/0305-0491(94)90135-X","url":null,"abstract":"<div><p>The relationship between ovarian steroidogenesis and the development of oogenesis was studied in the ovary of <em>Trichogaster trichopterus</em> by histological examination and thin layer chromotography. The percent yield of 17β-estradiol (E<sub>2</sub>) was high at a number of different stages of vitellogenesis, while those of 17α,20β-dihydroxy-4-pregnen-3-one (17,20-P) and testosterone (T) were high at the beginning of maturation, and increased steadily during this process. The per cent yields of T and 17α-hydroxyprogesterone (17-P) were low at all stages of vitellogenesis (VTG). For androstenedione (AS), 5-androstane-3β-ol-17-one, 5β-pregnane-3α,17α,20α-triol and 11-ketotestosterone, the per cent yields appeared to increase mainly during maturation and ovulation. It is suggested that the main pathways of steroidogenesis during oogenesis are: at VTG, [P]→[17-P]→[AS]→[E<sub>2</sub>]; and at maturation [17-P] → [17,20-P], the latter controlled by male stimulation of GtH.</p></div>","PeriodicalId":100294,"journal":{"name":"Comparative Biochemistry and Physiology Part B: Comparative Biochemistry","volume":"109 4","pages":"Pages 715-723"},"PeriodicalIF":0.0,"publicationDate":"1994-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/0305-0491(94)90135-X","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"77513101","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: 10
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