Lack of temperature-sensitivity of rat liver pyruvate kinase (Short Communication)

Rat liver pyruvate kinase, prepared by Sephadex treatment of a 10(5)g supernatant in phosphate buffer, is quite stable and gives reproducible results when a variety of parameters are altered in the enzyme assay. Incubation of this preparation at 25 degrees C or 0-2 degrees C has no effect on the activation by fructose 1,6-diphosphate or inhibition by ATP or alanine.     

Effect of Antilymphocytic Serum on Circulating Interferon in Mice as a Function of the Inducer

MOST investigators concerned with interferon synthesis in vivo have used the experimental procedure described by Baron and Buckler¹, in which circulating interferon is induced by intravenous administration of viruses. When interpreting results, however, it is difficult to know which cells are responsible for circulating interferon synthesis in the animal. Using a radiobiological approach, we have shown that after an intravenous injection of virus, interferon released into the blood stream of mice originates in cell populations of varying radiosensitivities, depending on the virus inoculated². Myxo-virus-induced circulating interferon production is characterized by high radiosensitivity, for serum interferon titres are decreased by more than 90% in C3H/He mice after one total body X-irradiation of 250 r. Moreover, the species specificity of interferon has enabled us to show that circulating interferon induced by Newcastle disease virus (NDV) is of donor type in xenogeneic radiochimaeras, from which we concluded that cells responsible for interferon synthesis with this virus originate from haemopoietic stem cells^3,4. Both granulocytes and lymphocytes fulfil the criteria of very radiosensitive elements derived from haemopoietic stem cells^5,6. We wish to report that myxovirus-induced circulating interferon production is selectively depressed after administration of antilymphocyte serum (ALS).     

Xylem perfusion of tap root segments of Plantago maritima: the physiological significance of electrogenic xylem pumps

Abstract A method is described for perfusing xylem vessels in tap root segments of the halophyte P. maritima. Use of excised segments allowed recording of the trans-root potential (TRP) at both ends of a segment. It was shown that there can be a spatial variation of electrogenic ion pump activity along the xylem in one root segment. The pH of perfusion solutions, differing in buffering capacity, was adjusted by the root segment to pH 5.1–5.6 during How through the xylem. This pH range was similar to that of sap produced by root pressure. The K⁺ activity in the outflow solution (K⁺_out) was rather constant at 12–13 mol m^?l3 despite input K⁺ activities ranging from 8 to 20 mol m^?l3. Addition of fusicoccin (10^?l2 mol m^?l3) to the perfusion solution induced a strong acidification of the xylem sap, a decrease in K⁺_out and an increase in Na⁺_out. Inhibition of aerobic respiration through anoxia inhibited electrogenic proton pumping into the xylem and led to an increase in K⁺_out and a decrease in Na⁺_out. It is suggested that transport of K⁺ and Na⁺ to the shoot of the halophyte P. maritima is regulated in the tap root by means of ion exchange between xylem vessels and xylem parenchyma and that this exchange is energized by proton translocating ATPases.     

Mode of Methomyl and Bipolaris maydis (race T) Toxin in Uncoupling Texas Male-Sterile Cytoplasm Corn Mitochondria

Bipolaris maydis race T toxin (BmT), and its functional analog, methomyl, uncoupled Texas male-sterile (T) cytoplasm mitochondria by decreasing the resistance of the inner membrane to protons. However, unlike protonophoric or ionophoric agents, BmT toxin and methomyl induced irreversible swelling. Packed volume measurements showed that mitochondrial volume was irreversibly increased by methomyl and BmT toxin indicating that mitochondria no longer functioned as differentially permeable osmometers. The decreased resistance of inner mitochondrial membranes to protons and the loss of osmotic volume regulation suggests that methomyl and BmT toxin induced the formation of hydrophilic pores in T mitochondrial inner membranes.     

绒毛膜促性腺激素及其α、β亚单位抗体的抗生育作用

本文研究结果证明给小白鼠子宫分别注射特异的抗hCG及其α、β亚单位血清后,唯有抗hCG及β亚单位血清能表现出显著的抗生育作用。这一结果在经纯化过的hCG及卢亚单位免疫球蛋白G的相同实验中也得到了验证。从而证实着床前的小白鼠胚泡中存在hCG样糖蛋白物质。 特别使人感兴趣的是这类抗体只对妊娠第三天的小白鼠胚泡的着床有明显的抑制效应,这是一个前所未曾遇见的问题。     

Photo-oxidative Degradation of Chlorophyll-a and Unsaturated Lipids in Liposomal Dispersions at Low-Temperature

Liposomal dispersions in water were used as a tool to study photo-oxidation of chlorophyll-a and photo-oxidation of unsaturated lipids at 1 or 4°C. The presence of monogalactosyl diglyceride stimulated chlorophyll-a degradation. In addition the level of linolenic acid was decreased in liposomal dispersions containing chlorophyll-a, dipalmitoyl phosphatidyl choline, and monogalactosyl diglyceride, indicating that monogalactosyl diglyceride and chlorophyll-a were coupled in the preparations. In liposomal dispersions containing equal (molar) quantities of a-tocopherol, monogalactosyl diglyceride, and chlorophyll-a, a-tocopherol fully protected linolenic acid against photo-oxidative degradation, while chlorophyll-a degradation was only slightly reduced. In liposomal preparations containing a-tocopherol, chlorophyll-a and phosphatidyl choline, a-tocopherol catalyzed degradation of chlorophyll-a. Absorption spectra of the liposomal dispersions showed that the presence of a-tocopherol caused increased absorption in red light, which was attributed to structural changes in the liposomal preparations and thus could explain the noted effects. Tocopherol itself was rapidly degraded in chlorophyll-a containing liposomal preparations. Complex formation between chlorophyll-a and monogalactosyl diglyceride in chloroplasts is suggested and protection by a-tocopherol against photo-oxidation in chilling-sensitive plants; a suggestion which is founded on the similarities that exist between chloroplast preparations and liposomal preparations containing chlorophyll-a and monogalactosyl diglyceride as regards photo-oxidative degradation of chlorophyll-a, a-tocopherol and linolenic acid.     

Effect of α-Tocopherol, β-Carotene, Monogalactosyldiglyceride and Phosphatidylcholine on Light-Induced Degradation of Chlorophyll a in Acetone

The effect of α-tocopherol, β-carotene, monogalactosyldi-glyceride and phosphatidylcholine on red light induced degradation of chlorophyll a was studied in acetone at 4°C. Monogalaclosyldi-glyceride was ineffective up to a molar ratio of monogalactosyldi glyceride to chlorophyll of 1:10. α-Tocopherol, β-carotene and phosphatidylcholine inhibited chlorophyll degradation. Maximal protection by α tocopherol and β-carotene was similar (76%) but on a molar basis a tocopherol was less effective. Protection by phosphatidylcholine was less than by a tocopherol and α-carotene but the lipid was effective at a lower ratio of chlorophyll to protectant. Inhibition by phosphatidylcholine was independent of the degree of unsaturation of the fatty acids. Effects of β-carotene and α-tocopherol were additive at suboptimal concentrations, but addition did not increase the maximal protection of 76% by these substances alone. Phosphatidylcholine increased the effectiveness of α-tocopherol and β-carotene independent of their concentrations. It is suggested that interactions between lipids participate in the mechanism protecting chlorophyll a against photooxidation in the chloroplast membrane.     

Influence of ecdysterone, precocene and compounds with juvenile hormone activity on induction, termination and maintenance of diapause in the parasitoid wasp, Nasonia vitripennis

ABSTRACT. Using the Galleria bioassay, no difference could be found between the JH titre of diapausing and developing Nasonia larvae. Compared to the values found in some Lepidoptera, the JH titres in Nasonia larvae are low, c. 14 Galleria units/g live weight. Induction of diapause could not be brought about by topical application of JH I, JH analogues, precocene, or ecdysterone to the maternal generation, nor by treating eggs or larvae with compounds with JH activity. Diapause was easily terminated by topical application of ecdysterone, however. If ecdysterone treatment was preceded by JH-treatment, the percentage of larvae terminating diapause was reduced: JH II seems to be more potent than JH I or JH III in this effect if the interval between JH and ecdysterone treatment is 72 h.