Determination of Rubella Hemagglutination-Inhibiting Antibody in Whole Blood

A technique is described for determination of rubella hemagglutination-inhibiting antibody in only 50 to 100 muliters of whole blood.     

Use of a New Buffer System with Formalinized Sheep Erythrocytes in the Rubella Hemagglutination-Inhibition Test

The increased sensitivity and improved agglutination and settling patterns of formalinized sheep erythrocytes in a new buffer, HEPES (N-2-hydroxyethylpiperazine N'-2'-ethanesulfonic acid), make this system more suitable for use in the rubella hemagglutination-inhibition test.     

Influence of added limestone and fertilizers upon the micro-nutrient content of forage tissue and soil

Summary Five rates of limestone and 4 rates of fertilizers were used in a split-plot design to study their effects under field conditions on Mo, Cu, B, Mn, and Zn levels in mixed forage tissue and soil, and on the forage yield. An increase in soil pH resulted in an increase in Mo and Cu content of plant tissue while B, Mn, and Zn decreased. The micro-nutrient content of the tissue increased as the harvesting season progressed. Increasing rates of applied fertilizer did not affect the micro-nutrient content of the forage tissue or soil. Liming to a pH of 5.6 and above reduced the availability of Mn and Zn in the soil. In general, the available B was low at pH values greater than 6.1. Lime did not affect the quantities of Mo and Cu in the soil. Manganese is supplied in large quantities by limestone and is not apt to be deficient in limed soil. However, addition of B and Zn may be required on the high pH soils of Eastern Canada in future. Molybdenum was adequate where the soil was limed to a pH of 6.1 or greater. The dry-matter yield of forage increased significantly with successive increases in lime up to pH 6.6 and with each increment of fertilization. Contribution No.226, Research Branch, Research Station, P.O. Box 1210, Charlottetown, P.E.I. and No.166, Experimental Farm, Nappan, N.S.     

Effect of N,P, and K on root yield and nutrient levels in the leaves and roots of rutabagas grown in a greenhouse

Summary Experiments were conducted to determine the influence of N, P, and K and of the NP and NK interactions on root yields and tissue concentrations of N, P, and K of rutabagas grown on a sandy loam soil under greenhouse conditions. Root yields were increased by applications of N and K but not by added P. The yield response to N was dependent on K supply. The highest dry matter content in roots was associated with the lowest rates of N and K and the lowest root yields. The N content of tissue at the early vegetative stage increased with increasing rates of N and decreased with increasing rates of P and K. The N content of root tissue at harvest increased at the highest rates of N but was unaffected by rates of P and K. The P and K content of root tissue increased with increasing rates of P and K, respectively. The levels of nutrients in early vegetative tissue associated with optimum yields were about 2.6, 0.24, and 2.0% for N, P, and K, respectively. The corresponding values in the leaf tissue at harvest were about 1.2, 0.12, and 1.5% N, P, and K, respectively. Contribution No.222.     

Inter-character relationships and heterosis observed in opaque-2 maize crosses and in their normal analogues

Summary Hybrids obtained from two series of diallel crosses made between six o ₂ converted inbred lines on the one hand and their normal analogues on the other were compared for twenty-five characters including yield and several of the yield components, including the parents. Observations on simple inter-character correlation coefficients presented here have shown that the majority of the correlations at the o ₂ level are of the same order as at the normal level. A number of correlations of the o ₂ type are inferior to those of their normal analogues, whereas a few are favoured by the o ₂ gene including the correlation of grain yield with kernels per row. A measure of heterosis for each hybrid over its mid-parent also demonstrated that the o ₂ types show poorer heterosis in more cases than do their normal counterparts. Still, in nearly 40 percent of the cases the o ₂ hybrids were found to be more heterotic than their normal analogues, particularly for the various maturity characters and several of the yield components. Thus, the possibility of improvement exists in breeding maize with the opaque-2 gene.     

Protein synthesis in rabbit reticulocytes: control of protein synthesis initiation by a met-tRNA Met f deacylase and peptide chain initiation factors

The 0.5M KCl wash of rabbit reticulocyte ribosomes (I fraction) catalyzes the deacylation of Met-tRNA_f^Met. Upon DEAE-cellulose column chromatography, the deacylase activity elutes with the 0.1M KCl wash of the column (f1) and is well-resolved from the peptide chain initiation factors (1–3). The deacylase activity is specific for Met-tRNA_f^Met (retic., $\text{E.}$$\text{coli}$). Other aminoacyl tRNAs tested including fMet-tRNA_f^Met (retic., $\text{E.}$$\text{coli}$), Phe-tRNA ($\text{E.}$$\text{coli}$), Val-tRNA (retic.), and Arg-tRNA (retic.) are completely resistant to the action of the deacylase. In the presence of the peptide chain initiation factor (IF1) and GTP, retic. Met-tRNA_f^Met forms the initiation complex Met-tRNA_f^Met:IF1:GTP (2), and in this ternary complex Met-tRNA_f^Met is not degraded by the deacylase. $\text{E.}$$\text{coli}$ Met-tRNA_f^Met binds to IF1 independent of GTP, and in this complex, this Met-tRNA_f^Met is degraded by the deacylase.Prior incubation of f1 with Met-tRNA_f^Met (retic.) strongly inhibited protein synthesis initiation, presumably due to deacylation of the initiator tRNA. This inhibition by f1 was completely prevented when Met-tRNA_f^Met (retic.) was pre-incubated with peptide chain initiation factors.     

Inhibition of protein synthesis directed by added viral and cellular messenger RNAs in extracts of interferon-treated Ehrlich ascites tumor cells. Location and dominance of the inhibitor(s)

Protein synthesis directed by exogenous (viral or cellular) messengers is impaired, but endogenous protein synthesis is not affected in an extract of interferon-treated Ehrlich ascites tumor cells (INT-extract). Protein synthesis directed by exogenous messengers is also impaired in a mixture of an INT-extract with an extract from control cells. This reveals that the impairment is due to one or more inhibitors in the INT-extract. The nondialyzability of the inhibitor(s) is probably an indication of large molecular size. In a not incubated INT-extract much of the inhibitory activity is in the high speed sediment fraction i.e., is presumably bound directly or indirectly to ribosomes. During incubation of the extract most of the inhibitory activity is released into the high speed supernatant fraction. The dose-response curve shows that in our conditions the translation of cellular messengers (from mouse L cells) is as sensitive to impairment by the inhibitor(s) as that of viral messengers (from reovirus or from encephalomyocarditis virus).