Diversity of extracellular proteases among Aeromonas determined by zymogram analysis

Aims: The current research was aimed at comparing extracellular proteolytic activities and zymogram profiles among Aeromonas spp. Methods and Results: Extracellular proteases of 47 strains of Aeromonas were analyzed by substrate (casein and gelatin) co‐polymerized SDS‐PAGE, and caseinolytic activity was determined using azocasein. Large variation on caseinolytic activity was evidenced. In general, the caseinolytic activity of Aeromonas hydrophila strains was significantly higher than that of other Aeromonas species. Several caseinolytic and gelatinolytic profiles were detected in Aeromonas. Cluster analysis allowed separating Aeromonas strains in four and three groups, based on their caseinolytic and gelatinolytic profiles, respectively. Although not specific patterns were evident, most Aer. hydrophila strains were clustered together and differed from Aeromonas caviae strains. The main caseinases of Aer. hydrophila were a serine protease with an apparent molecular weight (AMW) of 56 kDa and a metalloprotease with AMW of 22 kDa. Gelatinase profiles were characterized by the presence of high molecular weight metalloproteases (84 and 93 kDa), although the most active enzyme was a serine protease with AMW of 56 kDa. Other new caseinases and gelatinases were detected in specific Aeromonas strains. Conclusions: Aeromonas strains exhibited several extracellular proteolytic profiles, with a larger inter than intraspecific variation. Moreover, zymogram analyses allowed identifying new caseinases and gelatinases in Aeromonas. Significance and Impact of the Study: This is the first report on the intra‐ and interspecific variation of proteolytic profiles in Aeromonas determined by zymogram analysis, including the detection of new caseinases and gelatinases in this genus.     

Separation and characterization of two chorismate-mutase isoenzymes from Nicotiana silvestris

Two isoenzymes of chorismate mutase (EC 5.4.99.5) were isolated and partially purified from leaves of diploid (2n=24) Nicotiana silvestris Speg. et Comes and from isogenic cells in a suspension culture originally established from haploid tissue. An isoenzyme denoted CM-1 (M _r=52,000) accounted for the major fraction of total activity recovered from suspension-cultured cells, while isoenzyme CM-2 (M _r=65,000) represented the major fraction of activity recovered from green leaf tissue. The ratio of isoenzyme levels from these two sources differed more than 20-fold. The subcellular location of isoenzyme CM-1 is known to be in the chloroplasts of green leaves or in proplastids of cultured cells, while isoenzyme CM-2 is located in the cytosol. Both isoenzymes were stable during partial purification, possessed broad pH optima for catalysis between 6.0 and 8.0, and were active without denaturation at temperatures at least as high as 45° C. Thiol reagents were unnecessary for either stability or activity of both isoenzymes. The affinity of isoenzyme CM-2 for substrate (K _m=0.24 mM) was almost an order of magnitude better than that of CM-1. The kinetic behavior of isoenzyme CM-1 was influenced by pH, while that of isoenzyme CM-2 was not. At pH 7.2, hyperbolic substrate-saturation curves (K _m=1.7 mM) were obtained for isoenzyme CM-1. At pH 6.1, however, isoenzyme CM-1 displayed relatively weak positive cooperativity, Hill plots yielding an n value of 1.2 At pH 6.1 the half-saturation ([S]_0.5) value was 2.5 mM.Abbreviations DEAE diethylaminoethyl - M _r molecular weight     

Detection of pullulanase in polyacrylamide gels using pullulan-reactive red agar plates

After electrophoresis, active pullulanase bands in acrylamide gels have been detected by overlaying and then incubating the gel on a replica gel containing 2.5% pullulan-reactive red conjugate and 2.1% agar. The enzyme activity is revealed as a clear band against a red background on the replica gel. The sensitivity of the replica plate is such that 0.0012 unit of Klebsiella aerogenes pullulanase can be detected easily. This procedure is effective in enzyme screening to distinguish pullulanase from other carbohydrases.     

淡色库蚊敏感品系与敌百虫抗性品系乙酰胆碱酯酶同工酶在发育过程中的变异

本文从电泳和酶活力两个方面观察和分析了淡色库蚊(Culex pipiens pullens Coq.)的敏感品系(SEN)和敌百虫抗性品系(RD)的AchE同工酶在整个发育过程中不同性别及身体不同部位产生的变异,从中获得了一些颇有意义的结果。 1.从SEN品系与RD品系AchE同工酶在整个发育过程中的比较发现,AchE质和量上的变异与敌百虫抗性的产生密切相关。 2.一切品系的各个发育阶段,在凝胶相同的位置上都有一条相同的AchE酶带,这是主带。 3.在SEN品系和RD品系的雌成蚊中,有一条活力很高的AchE慢带,此带仅在雌成蚊的胸部存在,显示了性别和部位差异,称它为特征性慢带。此带的活力,RD品系高于SEN品系。 4.以三带喙库蚊(Culex tritaeniorhychus)的敏感品系及其抗双硫磷品系与淡色库蚊作比较,发现其雌、雄成蚊中除共有的主带外,还有一条较主带稍慢的AchE带,此带相当于淡色库蚊雌成蚊中的特征性慢带,但不存在性别差异,此带的泳动速度要略快于特征性慢带。 5.雌成蚊胸部的特征性慢带轻胰蛋白酶的限制性处理后,泳动位置发生改变,变动后的新位置恰与三带喙库蚊慢带的位置相同。两种库蚊在进化上似乎存在着某种联系。位移后的特征性慢带活性未变。 6.用伴性红眼区分幼虫性别后发现,淡色库蚊不同性别的幼虫和蛹,都存在1—3条向正极移动但活     

Soluble proteins and isoenzymes from seeds of diverse male steriles of sorghum, (Sorghum bicolor (L.) Moench)

Summary A comparison of soluble protein, esterase, GDH and ADH isoenzyme patterns in seeds of different steriles, maintainers and restorer lines exhibited similarities as well as differences. Soluble protein patterns from sterile and maintainer lines differed both qualitatively and quantitatively. Based on the esterase patterns, male steriles with different cytoplasms could be separated into three groups (i) Ck 60A and B; Nagpur A and B, (ii) M 35-1A and 1 B, M 31-2A and 2B, (iii) G1A and B, VZM2A and 2B. Each group could further be differentiated on the basis of minor differences in esterase isoenzyme patterns within each group. ADH and GDH patterns in general were similar in both sterile and maintainer lines.Abbreviations ADH Alcohol dehydrogenase - GDH Glutamate dehydrogenase - NAD Nicotinamide adenine dinucleotide     

Biosystematic studies onCapsella bursa-pastoris (Brassicaceae): Enzyme polymorphism in natural populations

The genetic variability of natural populations ofCapsella bursapastoris in North- and Middle-Europe has been estimated by means of enzyme assays. Zymograms of 81 populations have been developed. 17 loci could be identified, and 8 of them can be heterozygous. Genetic variability is greater between populations than within. No correlation between actual population sizes and genetic heterogeneity could be detected. Some electromorphs shift their frequencies proportionally to increasing adversity of climatic conditions, some appear to be constant over the whole area, and others are characterized by an apparently irregular variation pattern. Marginal populations comprise a significantly higher proportion of heterozygous plants than central ones. Apart from this clinal variation pattern, a mosaic pattern, strongly related to habitat conditions, was observed: genetic heterogeneity is greater in more intensively disturbed sites. The pattern of genetic variation in natural populations ofCapsella bursa-pastoris is rather highly influenced by the breeding system.     

Bioluminescent Assay of Total and Brain-Specific Creatine Kinase Activity in Cerebrospinal Fluid

Abstract: A bioluminescent assay based on the firefly luciferase reaction has been used for determination of creatine kinase activity in CSF. Activities as low as 0.1 U/L can be measured. The coefficient of variation at an activity level of 0.3–0.4 U/L was between 5 and 6%. The assay conditions optimized for serum specimens can be used for CSF. The adenylate kinase activity is almost completely inhibited, which simplifies the procedure. The creatine kinase (CK) isoenzyme distribution was obtained using the bioluminescent assay in combination with immunoinhibition or ion exchange chromatography. All specimens contained both MM and BB activity, but no MB was found. The study indicates that the bioluminescent assay is useful in the determination of CK isoenzymes in CSF. The clinical importance of the observed CK levels will be reported in a separate communication.     

The occurrence of chloroplastic and cytosolic isoenzymes of phosphoglycerate kinase in a range of plant species

The chloroplastic and cytosolic isoenzymes of phosphoglycerate kinase (PGK; EC 2.7.2.3) of leaves from 18 of a broad range of 21 vascular plant species were separated by either standard or modified anion-exchange Chromatographic procedures. Immunoprecipitation of the isoenzymes with antisera raised against barley chloroplastic and cytosolic PGK isoenzymes showed that the chloroplastic isoenzymes resemble the chloroplastic isoenzymes of other species more closely than the cytosolic isoenzyme of the same species and vice versa for the cytosolic isoenzymes. Each of the two cyanobacterial species tested, yielded only a single PGK fraction on anion-exchange chromatography and gave no reaction with antisera raised against the barley isoenzymes. The cyanobacteria are presumed to contain only a single PGK which is not closely related to either of the barley PGK isoenzymes. In all of the investigated leaf extracts the catalytic activity of the cytosolic PGK was exceeded by that of the chloroplastic PGK with the ratio for many of the C₃ plants falling within the range 595 to 1585 (cytosolic: chloroplastic). The relative amounts of cytosolic PGK activity appeared to be greater in older leaves, in C₄ and CAM plants and in ferns.Abbreviations CAM crassulacean acid metabolism - pgk phosphoglycerate kinase This work was supported by the Science and Engineering Research Council (grant no. GR/E54504) and also the King's College London Research Strategy Fund.     

白细胞酯酶同工酶对胃癌诊断价值的探讨

本文应用薄平板等电聚焦电泳法对15例未经手术治疗的胃癌患者进行了外周血白细胞酯酶同工酶的分离.结果:正常人外周血白细胞酯酶同工酶显示12条带,等电点(PI)为3.73～7.80.胃癌患者显示11条带,与正常相比第十二条带缺如,PI为3.80～7.90.同工酶各分带与正常相比,酶活性发生明显异常(P<0.01).提示;胃癌患者酯酶同工酶的改变可能是胃癌早期诊断的酶学指标.     

Segregation and linkage relationships of isoenzymes in shortleaf pine (Pinus echinata Mill.)

 Segregation and linkage relationships were analyzed between 28 isoenzyme loci in ten natural stands representing much of the natural range of Pinus echinata Mill. (shortleaf pine). A total of 203 possible two-locus combinations were tested. Three linkage groups were revealed in this study at a linkLOD of 4.0. The first linkage group (A) consisted of Pgi and Adh-1; Gdh, Idh, Skdh-2, G6pd-2 and Aco were mapped to the second linkage group (B); the third group (C) had 2 loci: Mdh-2 and Mdh-3. A moderate linkage between Mnr-2 and Dia-2 and weak linkages between Mnr-1 and Dia-1, and Got-2 and 6pgd-2 were also detected. The significance of these results in shortleaf pine is discussed and compared to linkage maps previously reported in other conifers, including pines. Received: 7 April 1997 / Accepted: 25 April 1997