Identification of Australian wheat cultivars by laboratory procedures: examination of pure samples of grain

1974 ◽  
Vol 14 (71) ◽  
pp. 796 ◽  
Author(s):  
CW Wrigley ◽  
KW Shepherd

Three laboratory procedures have been examined for the identification of about fifty wheat cultivars currently grown in Australia. The most discriminating of these methods is starch gel electrophoresis of gliadin proteins extracted from a single grain or from meal. This procedure is capable of identifying many of the cultivars directly. However, in some cases identification is complicated by the observation of more than one biotype for a cultivar on the basis of this test. By comparison, a larger number of grains can be examined by the qualitative phenol test but it is less discriminating. Additional information is provided by applying the test to glumes. Thirdly, quantitative assessment of grain hardness, measuring either particle size index or pearling resistance, gives a division of cultivars into about five groups. Specific results are listed for all methods so that the most suitable procedure can be chosen for distinguishing a particular group of cultivars.


1982 ◽  
Vol 33 (3) ◽  
pp. 409 ◽  
Author(s):  
CW Wrigley ◽  
PJ Robinson ◽  
WT Williams

The gliadin protein compositions of 79 wheat genotypes from Australia, New Zealand and North America, and one rye cultivar have been examined by starch gel electrophoresis. Interrelationships in the patterns thus obtained were investigated using a computer-generated inverse minimum spanning tree. Certain components were frequently found to occur together, presumably because their synthesis is controlled by closely linked genes. In addition, by using a network-generating program, associations between gliadins and many morphological (plant, head and grain), agronomic and quality attributes were studied. In many cases, specific gliadin components were found to be closely associated with certain attributes. In such cases a direct cause and effect cannot be inferred, but the approach indicates associations that warrant further study.



1964 ◽  
Vol 12 (01) ◽  
pp. 126-136 ◽  
Author(s):  
Karl H. Slotta ◽  
J. D Gonzalez

SummaryWhen urea or ε-amino caproic acid were used as solublizing agents for plasminogen in electrophoretic experiments, only one broad band of the proenzyme was obtained on acetate cellulose, in starch block, and in acrylamide gel. In starch gel electrophoresis, however, both forms of plasminogen – the native or euglobulin and Kline’s or Pseudoglobulin plasminogen – separated into six bands. These migrated toward the cathode at room temperature in borate or veronal buffer in the alkaline range and showed full activity in fibrinagar-streptokinase plates.



Genetics ◽  
1973 ◽  
Vol 74 (4) ◽  
pp. 595-603
Author(s):  
D Borden ◽  
E T Miller ◽  
D L Nanney ◽  
G S Whitt

ABSTRACT The isozymic patterns of tyrosine aminotransferase, NADP malate dehydrogenase, NADP isocitrate dehydrogenase, and tetrazolium oxidase were examined by starch-gel electrophoresis in Tetrahymena pyriformis, syngen 1. The genetics of the alleles controlling these enzymes was studied through a breeding program. Each enzyme locus was shown to assort vegetatively, as do other loci in this organism. A detailed analysis of the assortment process for the tyrosine aminotransferase locus indicated that the rate of stabilization of heterozygotes into pure types was essentially identical to previously-reported rates for other loci.



1963 ◽  
Vol 41 (1) ◽  
pp. 369-387 ◽  
Author(s):  
J. M. Neelin

By varying conditions of starch gel electrophoresis, factors contributing to the resolution of myogen proteins from chicken breast muscle have been studied. Variables examined included composition of the myogen extractant, protein concentration, ionic strength of electrophoretic media, pH of gel media, plane and direction of electrophoresis, and the nature of cations and anions in gel media and bridge solutions. The significance of anions was more closely studied with constant buffer systems, and gradient systems in which bridge electrolyte differed from, and gradually altered, the gel medium. Optimal separation was obtained in gradient systems with 0.10 M sodium chloride bridge solutions, and gel media of sodium cacodylate, pH 6.9, μ 0.010, which resolved 12 cationic zones, and sodium veronal, pH 7.4, μ 0.010, which resolved 10 anionic zones. These buffers in two-dimensional sequence revealed a total of about 24 components in this myogen.



1981 ◽  
Vol 59 (5) ◽  
pp. 771-775 ◽  
Author(s):  
Moira M. Ferguson ◽  
David L. G. Noakes ◽  
Roy G. Danzmann

Examination of 17 presumptive gene loci by starch-gel electrophoresis revealed differential mobilities only at acid phosphatase-1, alcohol dehydrogenase, esterase-1, and phosphoglucomutase between Nocomis biguttatus and N. micropogon. No intraspecific variation was observed for any loci. The genetic identity (I) and genetic distance (D) were 0.874 and 0.134, respectively. The correlation of electrophoretic mobilities and nuptial tubercle pattern in sexually dimorphic males supports the present taxonomic distinction of these species and provides a simple, unambiguous means of identifying any individuals.Stepwise discriminant function analysis of a series of mensural characters was used to compare fish identified as to species by electrophoresis. At best this correctly assigned fish to their respective species in 85.7% of cases, with a probability of misclassification of 0.1335.This study suggests these two are sibling species, based on a comparison of biochemical and morphological differentiation.



1967 ◽  
Vol 120 (2) ◽  
pp. 255-267 ◽  
Author(s):  
Koichiro Aoki ◽  
Joji Hori ◽  
Kazuro Kawashima


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