Role of carbohydrate as an antigenic determinant of a glycoprotein from rye-grass (Lolium perenne) pollen.

The carbohydrate component of Glycoprotein 2 (12% carbohydrate) from rye-grass (Lolium perenne) pollen has saccharide sequences that contribute to its antigenicity. Radioimmunoassay inhibition tests show that the antiserum to this glycoprotein cross-reacts with a number of other plant glycoproteins. In contrast, antiserum to another glycoprotein from rye-grass pollen, Glycoprotein 1 (5% carbohydrate), does not cross-react with any of the test glycoconjugates. Treatment of glycoproteins with sodium metaperiodate (0.02 M, 4 degree C, 6 h, in the dark) causes the loss of their ability to cross-react antigenically with Glycoprotein 2, and a loss of capacity to bind 125I-labelled concanavalin A. The cross-reactivity of this plant glycoprotein with other glycoconjugates imposes limitations on the interpretation of ultrastructural studies aimed at localizing a particular glycoprotein to a cellular site by using fluorescent or ferritin-labelled antisera. A radioimmunoassay inhibition technique for quantitative determination of the amounts of antigens in plants is also described.     

Immunofluorescent localization of two water-soluble glycoproteins including the major allergen from the pollen of ryegrass,Lolium perenne

Summary Two major glycoproteins have been localized in sectioned grains of ryegrass pollen by direct and indirect immunofluorescence methods using Fluorescein isothiocyanate (FITC)-labelled IgC fractions of antisera. These glycoproteins are the major allergen Group 1 allergen, and a principal antigen Antigen A. Four methods of fixation were employed: freeze-drying, methanol, 2.5% glutaraldehyde and 4% paraformaldehyde for 1 h at 4°C. The post-embedding staining technique of immunocytochemistry was used: anthers were embedded directly, or after dehydration, in JB-4 plastic resin and antibody reacted with sectioned pollen.The effects of these fixatives on the antibody combining sites of the antigens were quantified by a solid phase radioimmunoassay using [¹²⁵I]protein A to measure antibody binding. Glutaraldehyde was the only fixative to significantly depress antibody binding of both Antigen A and Group 1 allergen to their homologous antisera. This radioimmunoassay was modified to reyeal that FITC conjugation to either antibody did not impair antigen binding. In mature pollen, these antigens were located in the cytoplasm and in the complex wall. In developing grains early in the maturation period, specific fluorescence was concentrated at the periphery of the cytoplasm.     

Alteration in cell division, morphology and motility induced by the toxic principle of lupinosis.

A number of experiments are described in which the effect of the toxins causing lupinosis on cell morphology and motility is examined. The toxins arrested cells in metaphase leading to abnormal profiles, and inhibited leucocyte migration. Similar results were obtained with colchicine on cell division and, from the evidence obtained, it is suggested that the mechanism of action of the two agents is similar and that the same binding sites are probably involved.     

Ubiquinone synthetic pathway in flagellation of Salmonella typhimurium.

Flagellation of Salmonella typhimurium was found to require a functional pathway for ubiquinone synthesis as well as growth in the presence of aliphatic or aromatic carboxylic acids. Selection for constitutive flagellation eliminated the requirement for growth in the presence of added carboxylic acids.     

The effect of cross-linking spectrin-actin complexes with band 4.1 on the state of polymerization of the actin

The polymerization of actin in the presence of spectrin tetramers and band 4.1 isolated from the human erythrocyte has been measured using a fluorescence energy transfer technique. The results show that the cross-linking of spectrin-actin complexes by band 4.1 results in a limited depolymerization of actin filaments and a concomitant rise in the critical actin concentration. The phenomenon may explain in part the existence of actin in the erythrocyte cytoskeleton as short oligomers rather than as long filaments.     

Ultrastructural Features of the Oral Region of Amicronucleate Paramecium tetraurelia in Autogamy1

ABSTRACT Amicronucleate Paramecium tetraurelia fails to develop an oral apparatus but resorbs the pre-existing one in the sexual cycle. Previous cytological studies have revealed the presence of a shallow, oral depression with a few scattered basal bodies after autogamy or conjugation. The present ultrastructural study of the ectoplasm beneath the oral depression revealed only the presence of a disorganized filamentous reticulum and small blocks of cytopharyngeal ribbons. In addition, beneath the oral depression, a large number of discoidal vesicles were found, similar to but larger in diameter than those normally associated with the cytopharynx of vegetative cells. The oral structures found in amicronucleates in autogamy might be remnants of the pre-existing oral apparatus, but the possibility that they were newly developed was not excluded. The morphogenetic interest of these structures was discussed. It is evident that amicronucleates in autogamy do not develop an extensive oral ultrastructural organization.     

论山东、辽宁寒武系炒米店组底部(古丈阶顶部)小凤凰虫(Fenghuangella Yang in Zhou et al.,1977)北大核心

本文对在山东济南市钢城区九龙山和辽宁东部大连市白家山寒武系炒米店组底部报道的小凤凰虫,进行了详细的描述及修订。根据与小凤凰虫共生的三叶虫对于华北地台区苗岭统与芙蓉统的界线进行了深入探讨,将产有小凤凰虫的Liostracina simesi-Placosema convexa组合带作为华北地台区苗岭统古丈阶最上部的一个化石带,而将Prochuangia mansuyi的首现作为华北地台区芙蓉统排碧阶的底界,对于华南斜坡相区和华北地台区苗岭统和芙蓉统之间界线划分和对比具有重要意义。