scholarly journals The Isolation and some properties of liquid crystalline substances from solanaceous plants infected with three strains of tobacco mosaic virus

Tobacco mosaic was the first disease shown to be caused by a filter-passing virus, and Beijerinck (1898) suggested as its cause a “contagium vivum fluidum", Since then many other theories have been advanced, but there has been little positive evidence to indicate whether the virus more nearly resembled organisms such as small bacteria or chemical molecules such as the larger proteins. Recently, however, Stanley has isolated from tobacco (1936a) and tomato (Stanley and Loring 1936) plants suffering from mosaic a protein which he describes as crystalline and as possessing the properties of the virus. When susceptible plants were inoculated with this protein at a dilution of 10 -9 they developed typical symptoms of the disease. The protein was obtained from infective sap by repeated precipitation with 40% saturated ammonium sulphate solution, and by adsorption on and washing from celite. The “crystals” described by Stanley were small needles produced by precipitation with acid ammonium sulphate. A number of statements in Stanley’s earlier paper (1935 more especially those dealing with the nitrogen content and the serological activity, made us doubt the purity of his product, and preliminary experiments with methods similar to those used for the preparation of suspensions of potato virus “X” (Bawden and Pirie 1936) gave us products with much higher precipitation end-points with antisera than those claimed by Stanley. We have now exchanged material with Dr. Stanley and find no gross differences in the activities of our respective products. We have found, however, that by further purification the protein in neutral solution can be obtained in liquid crystalline states. Also, as will be shown later, there are considerable differences in the chemical descriptions given of the virus protein; some of these differences have already been resolved, and others presumably will be by future work.

Parasitology ◽  
1935 ◽  
Vol 27 (3) ◽  
pp. 450-460 ◽  
Author(s):  
Kenneth M. Smith

The symptoms produced by a green strain of tomato streak virus 1 upon a variety of Solanaceous plants are described. A yellow variant of the streak virus which appears to have arisen during the culturing of the green strain is also described. This variant produces local yellow spots upon all inoculated leaves of White Burley tobacco.Healthy tobacco plants have been infected with the green strain of the streak virus by spraying them with a virus suspension from an atomiser.The behaviour of the green and yellow virus strains when, co-existing in the tobacco plant is discussed.Filtration through graded collodion membranes shows that the two strains have different filtration end-points and that therefore they can be separated by this means. The difference in filterability is considered to be a quantitative effect and cannot yet be assigned to difference in particle size.Immunity tests have shown that a complete cross-immunity exists between the green and yellow strains of streak themselves, between them and two other strains of streak which produce local lesions and between the green and yellow strains and tobacco virus 1. No immunity was found between the streak viruses and those of tobacco necrosis, tobacco ringspot, tomato spotted wilt and potato virus X.The yellow strain of streak produced local yellow spots on mature leaves of White Burley tobacco. This suggests that the chlorophyll is actually attacked by the virus, and that the formation of the chlorotic spots is not due merely to the inhibition of plastid formation by the virus.


Author(s):  
R. Morris

Summary A simple, economical method is described for the radioimmunoassay of cortisol in serum. Extraction is avoided by heating the diluted serum to inactivate cortisol-binding globulin. The radioimmunoassay is carried out in a single disposable scintillation vial without centrifugation. Free and bound steroid is separated by partition between ammonium sulphate solution and liquid scintillation fluid. Accuracy, precision and sensitivity are satisfactory. Normal ranges obtained are comparable to those obtained by other radioimmunoassay methods for cortisol.


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