INHERITANCE OF ELECTROPHORETIC VARIANTS OF SERUM ESTERASES IN DOMESTIC FOWL

1968 ◽  
Vol 10 (4) ◽  
pp. 961-967 ◽  
Author(s):  
A. A. Grunder
Keyword(s):  
Gel Electrophoresis ◽  
Esterase Activity ◽  
Domestic Fowl ◽  
Staining Intensity ◽  
Starch Gel Electrophoresis ◽  
Electrophoretic Variants ◽  
Region I ◽  
Starch Gel ◽  
The Mean

Three regions of serum esterase activity of chickens were differentiated by means of starch gel electrophoresis and appropriate stains. Regions I and II seemed to represent aliesterase while region III apparently represented a cholinesterase. The patterns of zones of region I were classified into three phenotypes named A, B, and AB and the hypothesis was proposed that these are controlled by two codominant alleles named EsA and AsB. The staining intensity of these esterase zones among adults was sex-associated in that the mean staining intensity of zones was greater in male than in female sera. Frequency of the EsB allele was 0.70, 0.76, and 0.85 in three meat lines.

INHERITED VARIANTS OF α1-ANTITRYPSIN: A NEW ALLELE PiN

1974 ◽  
Vol 16 (2) ◽  
pp. 297-303 ◽  
Author(s):  
Diane Wilson Cox ◽  
Lynne Celhoffer
Keyword(s):  
Gel Electrophoresis ◽  
Null Allele ◽  
Starch Gel Electrophoresis ◽  
Electrophoretic Variants ◽  
Similar Region ◽  
New Variant ◽  
Starch Gel ◽  
Immunofixation Electrophoresis ◽  
Starch Gels ◽  
Antigen Antibody

A new inherited variant of α1-antitrypsin (protease inhibitor or Pi) has been found in five individuals of a family of Welsh origin. The new allele is called PiN, as the α1AT product migrates in acid starch gel between the products of the PiM and PiP alleles. The individuals carrying the PiN allele are all of Pi type MN. The new variant has been compared in several electrophoretic systems with other variants migrating in a similar region by acid starch gel electrophoresis (M, P, S, V, W and X). Acid starch gel and crossed antigen-antibody electrophoresis are most suitable for distinguishing the PiN product. By immunofixation electrophoresis, N has a mobility only slightly different from that of M, however the value of this method can be seen for distinguishing other slow variants which cannot be clearly distinguished on acid starch gels. Twenty-three variants of α1AT are now known. Twenty-two of these are electrophoretic variants and one, the null allele (Pi−), produces no α1AT.

scholarly journals ELECTROPHORETIC SEPARATION OF ESTERASES OF PULMONARY ALVEOLAR CELLS

1970 ◽  
Vol 18 (3) ◽  
pp. 167-177 ◽  
Author(s):  
ROBERT SCHIFF ◽  
MARY ANN BRUNSTETTER ◽  
ROBERT L. HUNTER ◽  
CARROLL E. CROSS
Keyword(s):  
Alveolar Macrophages ◽  
Gel Electrophoresis ◽  
Esterase Activity ◽  
Spectrophotometric Analysis ◽  
Starch Gel Electrophoresis ◽  
Electrophoretic Separation ◽  
Alveolar Cells ◽  
Additional Band ◽  
Female Mice ◽  
Starch Gel

Starch gel electrophoresis and vertical flat bed electrophoresis in polyacrylamide gels were used to separate butyrylesterases of pulmonary alveolar macrophages (PAMs) from RF/Al(+) and RF/Al(–) mice. PAM esterases from (+) mice showed five bands in starch and five or six in acrylamide whereas four and three or four bands, respectively, were found in extracts from (–) animals. The additional band or bands present only in positive samples corresponded to the Es-2 prealbumin serum esterase found only in the RF/Al (+) animals. This isozyme was more sensitive to diisopropylfluorophosphate than any other PAM esterase. The serum counterpart was sensitive to the same degree. None of the macrophage esterases were inhibited by eserine sulfate. Spectrophotometric analysis of serum esterase activity indicated a statistically significant increase in female mice from both sublines as compared to their respective males, but did not show a difference between the two sublines. The usefulness of the esterase marker in studies of PAM origin and pathologic conditions is discussed.

The systematic status of the lagoon periwinkle, Littorina tenebrosa

1999 ◽  
Vol 79 (4) ◽  
pp. 653-660 ◽  
Author(s):  
Iain F. Wilson ◽  
Elizabeth M. Gosling ◽  
William Tapper
Keyword(s):  
Phylogenetic Analysis ◽  
Genetic Variation ◽  
Gene Flow ◽  
Genetic Distance ◽  
Gel Electrophoresis ◽  
Distinct Group ◽  
Starch Gel Electrophoresis ◽  
Allopatric Populations ◽  
Starch Gel ◽  
The Mean

Eight samples of Littorina tenebrosa and L. saxatilis (Mollusca: Gastropoda) from Ireland and Britain, including pairs of each form from two locations in Ireland, were screened for genetic variation at 12 polymorphic enzyme loci using starch gel electrophoresis. Levels of polymorphism and heterozygosity were similar in L. tenebrosa and L. saxatilis, apart from a sample of L. tenebrosa from Britain which was less polymorphic than the Irish samples. No alleles were found to be unique to either form. Phylogenetic analysis using UPGMA showed that L. saxatilis and L. tenebrosa populations clustered as a monophyletic group. Nevertheless, the mean genetic distance between parapatric populations of L. saxatilis and L. tenebrosa (D=0.076) was similar to the mean for allopatric populations of either species (D=0.080). This indicates that there is a barrier to gene flow between the two forms Despite this, L. tenebrosa does not merit specific status since populations of this snail do not cluster as a distinct group, separate from L. saxatilis populations.

Electrophoretic Variants of L-Alpha-Glycerophosphate Dehydrogenase in Pacific Ocean Perch (Sebastodes alutus)

1970 ◽  
Vol 27 (5) ◽  
pp. 943-945 ◽  
Author(s):  
A. G. Johnson ◽  
F. M. Utter ◽  
H. O. Hodgins
Keyword(s):  
Pacific Ocean ◽  
Genetic Variants ◽  
Gel Electrophoresis ◽  
Population Studies ◽  
Starch Gel Electrophoresis ◽  
Electrophoretic Variants ◽  
Glycerophosphate Dehydrogenase ◽  
Starch Gel

Three phenotypes of L-alpha-glycerophosphate dehydrogenase (α-GPDH) were found in muscle extracts of Pacific ocean perch by starch-gel electrophoresis. No association was obvious between alpha-glycerophosphate phenotype and sex or stage of maturity. The observed phenotypes were presumed to be under the control of two allelic genes, F and S. This assumption was supported by the distribution of phenotypes of fish collected off the coasts of Washington and Oregon. This report is the first on genetic variants of an enzyme in Pacific ocean perch and suggests that isozymes of α-GPDH may be useful in population studies of this species.

Haemolymph esterases in the female larval honeybee, Apis mellifera L., during caste development

1968 ◽  
Vol 46 (5) ◽  
pp. 1013-1017 ◽  
Author(s):  
Ram K. Tripathi ◽  
S. E. Dixon
Keyword(s):  
Apis Mellifera ◽  
Gel Electrophoresis ◽  
Esterase Activity ◽  
Starch Gel Electrophoresis ◽  
Prepupal Stage ◽  
General Increase ◽  
General Decline ◽  
Starch Gel ◽  
Caste Development ◽  
Esterase Patterns

The haemolymph esterase patterns were obtained for eight ages during larval development of the two female castes of the honeybee, Apis mellifera L., by starch gel electrophoresis. Qualitatively, the patterns differed markedly with age within and between the castes. Quantitatively, esterase activity is higher in workers up to 72 hours of age and thereafter shows a general decline, whereas in queens the activity is lower up to 72 hours of age and is followed by a general increase. In both castes the activity is slightly increased towards prepupal stage. The significance of these results is discussed in relation to female dimorphism.

Biochemical Genetics of Fundulus heteroclitus (L.): V. Inheritance of 10 Biochemical Loci

1988 ◽  
Vol 79 (5) ◽  
pp. 359-365 ◽  
Author(s):  
D. C. Brown ◽  
I. J. Ropson ◽  
D. A. Powers
Keyword(s):  
Gel Electrophoresis ◽  
Fundulus Heteroclitus ◽  
Tissue Specificity ◽  
Intracellular Localization ◽  
Natural Populations ◽  
Starch Gel Electrophoresis ◽  
Biochemical Genetics ◽  
Linkage Groups ◽  
Electrophoretic Variants ◽  
Starch Gel

Abstract Starch gel electrophoresis has shown that natural populations of Fundulus heteroclitus have electrophoretic variants for at least 21 loci. We provide inheritance data for 10 polymorphic systems: esterases (Est-B, EST-C, and Est-D); aspartate amlnotransferases (Aat-A, and Aat-B); mannosephosphate isomerase (Mpl-A); acid phosphatase (Ap-A); phosphoglucomutase (Pgm-B); hexose-6-phosphate dehydrogenase (H6pdh-A); and fumarase (Fum-A). Variants for nine of these loci segregate as autosomally inherited codominant alleles. The other system, EST-C, does not reflect such inheritance. We have identified two possible linkage groups: H6pdh-A may be loosely linked to Pgm-B, and Fum-A appears to be linked to Pgm-A. Tissue specificity and intracellular localization for all these loci are also presented.

Allozyme divergence and evolutionary relationships among Populus deltoides, P. nigra, and P. maximowiczii

Genome ◽  
1990 ◽  
Vol 33 (1) ◽  
pp. 44-49 ◽  
Author(s):  
Om P. Rajora ◽  
Louis Zsuffa
Keyword(s):  
Gel Electrophoresis ◽  
Populus Deltoides ◽  
Genetic Identity ◽  
Starch Gel Electrophoresis ◽  
Root Tips ◽  
Frequency Distributions ◽  
Starch Gel ◽  
The Mean ◽  
Populus Species ◽  
Allozyme Loci

Horizontal starch gel electrophoresis of enzymes was used to study genetic divergence among Populus deltoides Marsh. (section Aigeiros Duby, Salicaceae), P. nigra L. (section Aigeiros), and P. maximowiczii Henry (section Tacamahaca Spach.) at 37 to 40 allozyme loci coding for 12 enzyme systems in root tips. These three Populus species were genetically distinct from each other. Populus deltoides, P. nigra, and P. maximowiczii had mutually exclusive alleles at two loci, and each of these species had unique alleles at many loci. Certain allozyme loci were detected only in one or two of these species. Frequency distributions of allozyme loci were bimodal with respect to genetic identity for comparisons between any two species. The mean genetic distance was 0.36 ± 0.10 between P. deltoides and P. nigra, 0.39 ± 0.09 between P. deltoides and P. maximowiczii, and 0.34 ± 0.10 between P. nigra and P. maximowiczii. The enzyme electrophoretic evidence indicated a monophyletic origin of the three Populus species.Key words: poplars, genetic identity and divergence, allozymes, molecular evolution, phylogenetics.

Sinapine Esterase. II . Specificity and Change of Sinapine Esterase Activity During Germination of Raphanus sativus

1980 ◽  
Vol 35 (11-12) ◽  
pp. 963-966 ◽  
Author(s):  
Dieter Strack ◽  
Gerhild Nurmann ◽  
Gesine Sachs
Keyword(s):  
Enzyme Activity ◽  
Gel Electrophoresis ◽  
Esterase Activity ◽  
Raphanus Sativus ◽  
Lag Phase ◽  
Starch Gel Electrophoresis ◽  
Rapid Degradation ◽  
Choline Esters ◽  
Starch Gel ◽  
Naphthyl Acetate

Abstract Following a 20 to 24 h lag-phase after sowing, the onset of both rapid degradation of sinapine (sinapolycholine) and rapid increase in sinapine esterase activity in cotyledons of Raphanus sativus was observed. After 2 days of germination maximal enzyme activity was reached and declined in subsequent germination stages as rapidly as it had appeared. Esterases, active against indophenyl acetate, showed highest activity in dry seeds, declining to more than 50% between the 1st and 3rd day of germination. Starch gel electrophoresis showed that all protein extracts contained a multiplicity of esterases, active against α-naphthyl acetate. When gels were incubated with sinapine, one new band appeared, stainable with diazotized ρ-nitroaniline. This band represents sinapine esterase activity. Tests for substrate specificity towards cinnamic acid choline esters showed highest enzyme activity with sinapine. Studies on the occurrence of sinapine esterase in other Brassicaceae revealed that the enzyme activity coincides with the occurrence and degradation of sinapine.

Subcellular localization and drug-Induced changes; of rat liver and kidney esterases

1968 ◽  
Vol 46 (2) ◽  
pp. 207-212 ◽  
Author(s):  
W. S. Schwark ◽  
D. J. Ecobichon
Keyword(s):  
Rat Liver ◽  
Gel Electrophoresis ◽  
Esterase Activity ◽  
Microsomal Fraction ◽  
Starch Gel Electrophoresis ◽  
Drug Induced ◽  
Liver Esterase ◽  
Liver And Kidney ◽  
Starch Gel ◽  
Induced Changes

The subcellular distribution of the esterases of rat liver and kidney was examined by differential centrifugation followed by quantitative titrimetric analysis, starch-gel electrophoresis, and electron microscopy of the subcellular fractions. The esterases were found primarily in the microsomal fraction of the cell. Soluble or cytoplasmic forms of esterases were also found. These conclusions were substantiated by induction studies with DDT and sodium phenobarbitone. Both drugs were capable of inducing liver esterase activity, DDT being more potent. In contrast to the liver, increased kidney esterase activity was not induced by these compounds.

scholarly journals Genetic variation of Abies alba Mill. in Polish part of Sudety Mts.

2014 ◽  
Vol 70 (3) ◽  
pp. 215-219 ◽  
Author(s):  
Andrzej Lewandowski ◽  
Maciej Filipiak ◽  
Jarosław Burczyk
Keyword(s):  
Gel Electrophoresis ◽  
Abies Alba ◽  
Silver Fir ◽  
Allozyme Polymorphism ◽  
Starch Gel Electrophoresis ◽  
Expected Heterozygosity ◽  
Starch Gel ◽  
The Mean ◽  
Allozyme Loci ◽  
Two Populations

The genetic structure of silver fir (<em>Abies alba</em> Mill.) was investigated among 8 populations from Sudety Mts. and 2 additional populations from other parts of Poland. Nine enzyme systems controlled by 13 allozyme loci were analyzed using starch gel electrophoresis. The mean expected heterozygosity, ranging from 0.06 to 0.11 and was lower compared to that found in other conifers. The mean genetic distance among all silver fir populations was 0.005. The Sudeten group of populations appeared to be genetically different from the two populations from other parts of Poland, indicating that at least two different centers are responsible for the current distribution of allozyme polymorphism in the tested populations.

Sign in / Sign up

Export Citation Format

Share Document