By Leslie A. Hickle, William L. Fitch
content material: Analytical chemistry of Bacillus thuringiensis : an summary / Leslie A. Hickle and William L. Fitch --
ancient points of the quantification of the energetic aspect percent for Bacillus thuringiensis items / George Tompkins, Reto Engler, Michael Mendelsohn, and Phillip Hutton --
Bioassay equipment for quantification of Bacillus thuringiensis [delta]-endotoxin / Clayton C. Beegle --
Specificity of insecticidal crystal proteins : implications for commercial standardization / R. Milne, A.Z. Ge, D. Rivers, and D.H. Dean --
In vitro analyses of Bacillus thuringiensis [delta]-endotoxin motion / George E. Schwab and Paul Culver --
id of entomocidal pollutants of Bacillus thuringiensis by means of high-performance liquid chromatography / Takashi Yamamoto --
Characterization of parasporal crystal pollutants of Bacillus thuringiensis Subspecies kurstaki traces HD-1 and NRD-12 : use of oligonucleotide probes and cyanogen bromide mapping / L. Masson, M. Bossé, G. Préfontaine, L. Péloquin, P.C.K. Lau, and R. Brousseau --
improvement of a high-performance liquid chromatography assay for Bacillus thuringiensis var. san diego [delta]-endotoxin / Leonard Wittwer, Denise Colburn, Leslie A. Hickle, and T.G. Sambandan --
Use of sodium dodecyl sulfate-polyacrylamide gel electrophoresis to quantify Bacillus thuringiensis [delta]-endotoxins / Susan M. Brussock and Thomas C. Currier --
Quantitative immunoassay of insecticidal proteins in Bacillus thuringiensis items / R. Gene Groat, James W. Mattison, and Eric J. French --
The light-scattering characterization of [delta]-endotoxin creation in inclusion our bodies / Fritz S. Allen, Betty J.M. Hannoun, Tammy B. Hebner, and Kathryn Nette --
Quantification of Bacillus thuringiensis insect keep an eye on protein as expressed in transgenic vegetation / Roy L. Fuchs, Susan C. MacIntosh, Duff A. Dean, John T. Greenplate, Frederick J. Perlak, Jay C. Pershing, Pamela G. Marrone, and David A. Fischhoff --
High-performance liquid chromatography research of 2 [beta]-exotoxins produced via a few Bacillus thuringiensis lines / Barry L. Levinson.
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Extra info for Analytical Chemistry of Bacillus thuringiensis
The authors suggest that extracellular virus gains intracellular access after a primary surface recognition and binding event involving the endotoxin receptor, and that toxin competitively inhibits binding of virus to the receptor. The possibility of shared receptor recognition regions in viral d toxi protei migh hav some bearing on evolutionar endotoxins. Î Brush Border Membrane Vesicles As stated in the preceding sections, the epithelium of the insect midgut is a complex multicompartmental system.
Assay pH is elevated as high as possible even though full toxin solubilization cannot be achieved. Plunpotentiality of some cell lines might obviate doubts concerning the relevance of findings obtained from cultured cells of non-midgut origin. Essentially, the broader relevance of information gleaned from cultured ceil systems is often challenged, but this rarely impacts on the ultimate utility of the in vitro approach. t kurstaki which had been enzymatically processed with gut proteases from T\ nL Cytotoxicity was completely abolished by heat treatment of the toxin, or by prior incubation of the toxin with specific antiserum, thereby confirming the protein identity of the toxic component.
ACS Symposium Series; American Chemical Society: Washington, DC, 1990. 38 ANALYTICAL CHEMISTRY OF BACILLUS THURINGIENSIS interaction at the apical membrane. This in turn leads to destruction of the potassium ion gradient as well as the potential difference across tne membrane. Subsequent to such disruption in the equilibrium provided by this gating mechanism would be a rise in the intracellular pH. t endotoxin-induced inhibition of the short circuit current in M . sexta midgut preparations. This in turn provided additional evidence for an endotoxin effect on transmembrane ion flux.