Enzyme variation in the Anopheles gambiae Giles group of species (Diptera: Culicidae)

1978 ◽  
Vol 68 (1) ◽  
pp. 85-97 ◽  
Author(s):  
S. J. Miles
Keyword(s):  
Anopheles Gambiae ◽  
Natural Populations ◽  
Lactic Dehydrogenase ◽  
Starch Gel Electrophoresis ◽  
Malic Dehydrogenase ◽  
Glycerophosphate Dehydrogenase ◽  
Starch Gel ◽  
Anopheles Gambiae Giles ◽  
Species Specific ◽  
Glucose 6 Phosphate Dehydrogenase

AbstractThe genotypes of chromosomally-identified individuals from natural populations of the known species of the group of Anopheles gambiae Giles were scored for the enzyme protein structural loci coding for adenylate kinase (Adk), α-naphthyl acetate esterase (Est-1, Est-2, Est-3), glutamic-oxaloacetic transaminase (Got), α-glycerophosphate dehydrogenase (αGpd), hexokinase (Hk), isocitric dehydrogenase (Idh), lactic dehydrogenase (Ldh), ‘leucine’ aminopeptidase (Lap-2), malic enzyme (Me), octanol dehydrogenase (Odh), phosphoglucomutase (Pgm-1, Pgm-2), 6-phosphogluconic dehydrogenase (6-Pgd), phosphohexose isomerase (Phi) and superoxide dismutase (Sod), following starch gel electrophoresis. In the material examined, Est-1, Est-2, Est-3, Got, ldh, Lap-2, Odh, Pgm-1, Pgm-2 and Sod were segregating for two or more alleles; unique alleles at the Est-1, Got and Sod loci produced species-specific phenotypes in A. melas (Theo.), species C and species D, respectively. The further sampling of A. merus Dön, populations supported the presence of a unique SOD phenotype by which this species can also be identified. Of the other enzyme systems examined, no activity following electrophoresis was detected for aldolase and fructose-1,6-diphosphatase, and the resolution of acid and alkaline phosphatase, glyceraldehyde-3-phosphate dehydrogenase, glucose-6-phosphate dehydrogenase, malic dehydrogenase and xanthine dehydrogenase was too poor under the particular electrophoretic conditions for genetic analyses of the enzyme phenotypes.

Comparative morphology of the cottid genus Myoxocephalus based on biochemical characters

1972 ◽  
Vol 50 (5) ◽  
pp. 683-693 ◽  
Author(s):  
Garry I. McT. Cowan
Keyword(s):  
East Coast ◽  
Comparative Morphology ◽  
Lactic Dehydrogenase ◽  
The Arctic ◽  
Nominal Species ◽  
Malic Dehydrogenase ◽  
Banding Patterns ◽  
Starch Gel ◽  
Asiatic Species ◽  
Species Specific

Specimens of 11 nominal species of the cottid genus Myoxocephalus were subjected to micro starch-gel electrophoretic analyses. Muscle myogens and isozymes of muscle lactic and malic dehydrogenases were examined.No sexual variations were evident in the electropherograms. Geographic variation in myogen characteristics was investigated for three species, two of which were of a homogeneous nature. In the third, M. scorpius, the specimens from Europe differed from all others.The myogen banding patterns were highly species-specific as were the shapes of their densitometer tracings. Two banding patterns were detected in malic dehydrogenase isozymes. Lactic dehydrogenase isozymes also evinced two distinct patterns, 11 species having one pattern and one (M. scorpioides) exhibiting both.On the basis of myogen data two natural groupings are evident, one composed of the Asiatic species and another of the Arctic and American east coast forms.

scholarly journals Enzyme variability in the Drosophila willistoni Group. V. Genic variation in natural populations of Drosophila equinoxialis

1972 ◽  
Vol 20 (1) ◽  
pp. 19-42 ◽  
Author(s):  
Francisco J. Ayala ◽  
Jeffrey R. Powell ◽  
Martin L. Tracey
Keyword(s):  
Genetic Variation ◽  
Allelic Variation ◽  
Natural Populations ◽  
Starch Gel Electrophoresis ◽  
Gene Frequencies ◽  
Group V ◽  
Neutral Genetic Variation ◽  
Starch Gel ◽  
Genic Variation ◽  
Standard Techniques

SUMMARYWe have studied genetic variation at 27 loci in 42 samples from natural populations of a neotropical species, Drosophila equinoxialis, using standard techniques of starch-gel electrophoresis to detect allelic variation in genes coding for enzymes. There is considerarle genetic variability in D. equinoxialis. We have found allelic variation in each of the 27 loci, although not in every population. On the average, 71% of the loci are polymorphic – that is, the most common allele has a frequency no greater than 0·95 – in a given population. An individual is heterozygous on the average at 21·8% of its loci.The amount of genetic variation fluctuates widely from locus to locus. At the Mdh-2 locus arout 1% of the individuals are heterozygotes; at the other extreme more than 56% of the individuals are heterozygous at the Est-3. At any given locus the configuration of allelic frequencies is strikingly similar from locality to locality. At each and every locus the same allele is generally the most common throughout the distribution of the species. Yet differences in gene frequencies occur between localities. The pattern of genetic variation is incompatible with the hypothesis that the variation is adaptively neutral. Genetic variation in D. equinoxialis is maintained by balancing natural selection.The amount and pattern of genetic variation is similar in D. equinoxialis and its sibling species, D. willistoni. Yet the two species are genetically very different. Different sets of alleles occur at nearly 40% of the loci.

Cytoplasmic Carboxylesterases of Human and Domestic Animal Liver: Aggregation, Dissociation and Molecular Weight Estimation

1972 ◽  
Vol 50 (1) ◽  
pp. 9-15 ◽  
Author(s):  
D. J. Ecobichon
Keyword(s):  
Molecular Weight ◽  
Human Liver ◽  
Gel Filtration ◽  
Domestic Animal ◽  
Starch Gel Electrophoresis ◽  
Weight Estimation ◽  
Animal Liver ◽  
Starch Gel ◽  
Species Specific ◽  
Two Peaks

The cytoplasmic carboxylesterases of bovine, ovine, equine and human liver were fractionated by starch gel electrophoresis and by gel filtration on Sephadex. While species-specific, heterogeneous bands were observed in starch gel, the esterases of the bovine, ovine and equine liver were eluted from Sephadex G-100 as single peaks of activity, each with a characteristic elution volume. Gel filtration of human liver extracts yielded two peaks of activity, one containing electrophoretically slow esterases, the other electrophoretically fast esterases. Extracted equine and human hepatic carboxylesterases aggregated readily on storage or concentration, forming larger units which could be dissociated by a combination of acidic pH and high salt concentration. Molecular weight estimates of the hepatic esterases by gel filtration on Sephadex G-100 and G-200 yielded values of 65 000 for ovine, 55 000 for bovine, 96 000 and 70 000 for equine variants and 180 000 and 65 000 for human variants. The observations suggested that the cytoplasmic enzymes in relatively crude hepatic extracts had a lower molecular weight than those in concentrated or partially purified preparations which formed stable dimers or trimers.

Inter-Species Relationships Within the Genus Oncorhynchus Based on Biochemical Systematics

1966 ◽  
Vol 23 (1) ◽  
pp. 101-107 ◽  
Author(s):  
H. Tsuyuki ◽  
E. Roberts
Keyword(s):  
Phylogenetic Relationships ◽  
Gel Electrophoresis ◽  
Plasma Proteins ◽  
Disc Electrophoresis ◽  
Starch Gel Electrophoresis ◽  
Species Relationships ◽  
Oncorhynchus Masou ◽  
Starch Gel ◽  
Specific Muscle ◽  
Species Specific

The species specific muscle myogens of Salmo gairdnerii, Oncorhynchus masou, O. masou ishikawae, O. kisutch, O. tshawytscha, O. keta, O. nerka, and O. gorbuscha are compared by starch gel electrophoresis. Plasma proteins of these same species are also examined by polyacrylamide disc electrophoresis. The range of usefulness of muscle myogens in species identification, and equally significantly, their value in establishing phylogenetic relationships of closely related groups, as the genus Oncorhynchus, are discussed. The myogen patterns of O. keta and O. gorbuscha from the Asiatic and North American coasts were found to be identical, further supporting the concept of absolute species specificity of these patterns.

Morphological and biochemical characterization of the trypanosomatids Crithidia desouzai and Herpetomonas anglusteri

1991 ◽  
Vol 69 (3) ◽  
pp. 571-577 ◽  
Author(s):  
Maria Cristina M. Motta ◽  
Antonio M. Sole Cava ◽  
Paulo M. F. Silva ◽  
João E. Fiorini ◽  
Maurílio J. Soares ◽  
...  
Keyword(s):  
Biochemical Characterization ◽  
Similarity Index ◽  
Starch Gel Electrophoresis ◽  
Electrophoretic Study ◽  
Monophyletic Cluster ◽  
Phosphogluconate Dehydrogenase ◽  
Unique Event ◽  
Enzyme Systems ◽  
Starch Gel ◽  
Glucose 6 Phosphate Dehydrogenase

Two species of trypanosomatids, Crithidia desouzai and Herpetomonas anglusteri, were recently isolated from Diptera in Minas Gerais, Brazil. The Crithidia species was found to harbor bacterium-like endosymbionts in the cytoplasm. To biochemically characterize these two species of trypanosomatids, and to try to verify the evolutionary meaning of the presence of endosymbionts, an electrophoretic study was undertaken whereby the two species were compared with eight other species in the same family. Horizontal 12.5% starch gel electrophoresis was used to resolve the isozymes of eight enzyme systems: acid phosphatase, glucose-6-phosphate dehydrogenase, hexokinase, malate dehydrogenase, malic enzyme, 6-phosphogluconate dehydrogenase, phosphoglucose isomerase, and phosphoglucomutase. Ten other enzyme systems were assayed without yielding any reproducible activity. The isozymes observed were conservatively interpreted as being due to the activity of 44 different alleles. All species studied differed in at least one enzyme system. The phenetic (Jaccard similarity index, UPGMA grouping) analysis produced a tree in which the species of Crithidia and Herpetomonas clustered separately, forming monophyletic groupings. All the endosymbiont-bearing species formed a monophyletic cluster, indicating that the presence of bacterium-like endosymbionts may be a synapomorphy of that group, and may represent, therefore, a unique event in the evolution of the genus.

CONGENITAL NONSPHEROCYTIC HEMOLYTIC ANEMIA ASSOCIATED WITH ERYTHROCYTE GLUCOSE-6-PHOSPHATE DEHYDROGENASE DEFICIENCY IN A NEGRO FAMILY

PEDIATRICS ◽  
1966 ◽  
Vol 37 (4) ◽  
pp. 624-629
Author(s):  
Aaron Grossman ◽  
K. Ramanathan ◽  
Parvin Justice ◽  
Joan Gordon ◽  
Nasrollah T. Shahidi ◽  
...  
Keyword(s):  
Enzyme Activity ◽  
Hemolytic Anemia ◽  
Gel Electrophoresis ◽  
Dehydrogenase Deficiency ◽  
Red Cells ◽  
Starch Gel Electrophoresis ◽  
Negro Family ◽  
Starch Gel ◽  
Normal Enzyme ◽  
Glucose 6 Phosphate Dehydrogenase

This paper describes a Negro family with congenital nonspherocytic hemolytic anemia associated with glucose-6-phosphate dehydrogenase deficiency. All four affected males in this family showed a hemolytic anemia characterized by low hemoglobin, reticulocytosis, and jaundice. There was no detectable G-6-P D in the red cells and about a tenth of normal enzyme activity in the white cells. By starch gel electrophoresis, the G-6-P D was present as a single band which migrated at the rate of 104% of normal. Physico-chemical studies revealed a marked increase of the Michaelis constant for both G-6-P and TPN, a marked lability of the enzyme upon heating at 40°C and 48°C, and a single narrow peak at pH 9.0. Most of these features were similar to those seen in the Oklahoma I variant. Four of the females in the family were studied (two sisters, the mother, and a maternal aunt of the propositus); all showed a lesser degree of anemia and reticulocytosis but no jaundice, except in the mother. There was a decrease of haptoglobins and both the mother and one sister showed a decrease of erythrocyte survival time as measured by chromium-51. The female members had between 11 and 26% of normal G-6-P D activity in the red cells and between 35 and 63% of normal enzyme activity in the white cells. Starch gel electrophoresis in the mother and aunt showed a single band which migrated at 110% of normal with a trail at the position of the affected males. The presence of a milder degree of hemolysis in the heterozygous carriers of the gene for G-6-P D deficiency associated with congenital nonspherocytic hemolytic anemia provides further support for the Lyon hypothesis in man.

Enzyme variation in Eimeria species of the chicken

Parasitology ◽  
1975 ◽  
Vol 71 (3) ◽  
pp. 369-376 ◽  
Author(s):  
M. W. Shirley
Keyword(s):  
Species Differences ◽  
Eimeria Species ◽  
Starch Gel Electrophoresis ◽  
Phosphogluconate Dehydrogenase ◽  
Glucose Phosphate ◽  
Parasite Stage ◽  
Starch Gel ◽  
Biochemical Identification ◽  
Glucose 6 Phosphate Dehydrogenase ◽  
First Time

A method for the biochemical identification of protozoa belonging to the genus Eimeria is described for the first time. Starch gel electrophoresis of the enzymes lactate dehydrogenase, glucose phosphate isomerase, 6-phosphogluconate dehydrogenase and glucose-6-phosphate dehydrogenase from parasite extracts revealed both intra- and inter-species differences when 11 strains representative of 6 species of Eimeria were examined. Oocysts were the most accessible parasite stage for investigation but sporozoites and merozoites of an embryo-adapted strain of E. tenella were also examined for enzyme activity.

Genetic variability in natural populations of the gray wolf, Canis lupus

1991 ◽  
Vol 69 (5) ◽  
pp. 1183-1188 ◽  
Author(s):  
Phyllis K. Kennedy ◽  
Michael L. Kennedy ◽  
Peter L. Clarkson ◽  
Ilme S. Liepins
Keyword(s):  
Genetic Variability ◽  
Spatial Heterogeneity ◽  
Canis Lupus ◽  
Gel Electrophoresis ◽  
Human Impacts ◽  
Natural Populations ◽  
Gray Wolf ◽  
Starch Gel Electrophoresis ◽  
Gray Wolves ◽  
Starch Gel

The genetic variability of gray wolves (Canis lupus) from northwestern Canada was assessed through starch-gel electrophoresis. Of 27 protein systems examined, 25, representing 37 presumptive loci, were consistently scorable; 7 proteins (5 were consistently scorable) exhibited polymorphism. The level of heterozygosity (3.0%) was medial relative to values reported for natural populations of Carnivora and high relative to values reported for natural populations of canids. An overall pattern of few deviations from Hardy–Weinberg expectations and some spatial heterogeneity was observed. Wolves associated with different caribou herds exhibited a low level of differentiation (FST = 0.029). The pattern of variability supports the view of a large panmictic population resulting from extensive movements of individuals and packs and from natural and human impacts on pack structure and formation.

scholarly journals COMPARATIVE STUDIES OF THE ISOZYMES OF LACTIC DEHYDROGENASE IN RABBIT AND MAN

1962 ◽  
Vol 116 (5) ◽  
pp. 797-806 ◽  
Author(s):  
Elliot S. Vesell ◽  
John Philip ◽  
Alexander G. Bearn
Keyword(s):  
Tissue Culture ◽  
Lactic Dehydrogenase ◽  
Isozyme Pattern ◽  
Ldh Activity ◽  
Starch Gel ◽  
Species Specific ◽  
Increased Activity ◽  
Rabbit Tissues

During development of rabbit tissues, characteristic sequential alterations in the LDH isozyme pattern occur, and consist for liver and muscle in loss of the most rapidly migrating anodal bands, and increased activity in the cathodal bands and slower migrating anodal bands. In heart the reverse changes were observed. Comparison of the isozyme patterns observed in various fetal and adult human tissues suggests that these same sequential alterations probably occur. A species-specific isozyme pattern is obtained in long term culture of rabbit, chick, and human cells. The alterations in tissue culture are characterized by a gradual redistribution of total LDH activity in which there is decreased intensity of rapidly migrating anodal bands. These sequential alterations are independent of the organ of origin. The number of bands observed in the starch gel is partly dependent upon the total activities applied. Isozymes may provide a convenient method for determining the species of origin of cell lines in common use and for investigating the effects of various alterations in the in vitro environment on cells grown in tissue culture.

ETUDE DE L'HEREDITE DE PHOSPHATASES ACIDES CHEZ LE DACTYLE (DACTYLIS GLOMERATA) DIPLOIDE ET TETRAPLOIDE

1981 ◽  
Vol 23 (3) ◽  
pp. 513-523 ◽  
Author(s):  
R. Lumaret
Keyword(s):  
Polymorphic Locus ◽  
Natural Populations ◽  
Dactylis Glomerata ◽  
Wild Plants ◽  
Starch Gel Electrophoresis ◽  
Ploidy Levels ◽  
Orchard Grass ◽  
In The Wild ◽  
Starch Gel ◽  
Dactylis Glomerata L

Starch gel electrophoresis of leaves of diploid and more particularly tetraploid orchard grass (Dactylis glomerata L.) from cultivars as well as natural populations disclosed several anodal stable bands with fast migration and phosphatasic activity. Six different phenotypes with one band, many others with three regular bands or six bands (only in the tetraploid individuals), were observed, showing the dimeric structure of the enzymes. Inheritance studies showed one polymorphic locus with six codominant alleles AcPH 11.00, AcPH 10.95, AcPH 10.90, AcPH 10.88, AcPH 11.02 and AcPH 11.04 with differences in enzymatic expression. AcPH 1.00 and AcPH 10.90 have been found in the two ploidy levels. Results from the tetraploid progenies involved tetravalents in meiosis for individuals originating from cultivars but bivalents in the wild plants. The two loci AcPH 1 and GOT 1 (this last one coding for a glutamate oxaloacetate transaminase) are not linked and seem to be located on different chromosomes.

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