Effect of various methods of immobilization on the stability of a microbial biosensor for surfactants based onPseudomonas rathonis T

The operating and storage stability of a receptor element of an amperometric biosensor based on thePseudomonas rathonis strain T capable of degrading surfactants was tested. Microbial cells were immobilized by incorporation in gels (agar, agarose, and calcium-alginate), polyvinyl alcohol membrane, adhesion to Chromatographic paper GF/A, or by cross-linking induced by glutaric aldehyde. Incorporation of microbial cells in agar gel provides long-standing conservation of their activity and viability during measurements of high concentrations of surfactants and allows the receptor element of the biosensor to be rapidly recovered after measurements.     

Collagen receptors mediate early events in the attachment of epithelial (MDCK) cells

Summary Madin-Darby canine kidney (MDCK) cells kept in suspension culture for 12–15 hr displayed high-affinity binding sites for¹²⁵I-lathyritic (soluble) collagen (120,000/cell,K _D =30nm) and preferred collagens types I and IV over laminin or fibronectin as substrates during the first hour of attachment. On the other hand, after 4 hr, attachment to all four substrates was equally efficient. Upon challenge with a collagen substrate, the high-affinity sites were rapidly recruited on it (T1/2=6 min). Their occupancy by soluble collagen triggered the exocytosis of a second large population of low-affinity collagen binding sites that included laminin and seems to be involved in a second cell-attachment mechanism. These results are compatible with a twostep model of MDCK cell attachment to the substrate: first, via high-affinity collagen binding sites, and second, via laminin of cellular origin.     

Prophylactic and curative effects of Bacopa monniera in gastric ulcer models.

Bacopa monniera Wettst. (BM, syn. Herpestis monniera L; Scrophulariaceae), is an Ayurvedic drug used as a rasayana. Its fresh juice was earlier reported to have significant antiulcerogenic activity. In continuation, methanolic extract of BM (BME) standardized to bacoside-A content (percentage-38.0 ± 0.9), when given in the dose of 10–50 mg/kg, twice daily for 5 days, showed dose-dependent anti-ulcerogenic on various gastric ulcer models induced by ethanol, aspirin, 2 h cold restraint stress and 4 h pylorus ligation. BME in the dose of 20 mg/kg, given for 10 days, twice daily showed healing effects against 50% acetic acid-induced gastric ulcers. Further work was done to investigate the possible mechanisms of its action by studying its effect on various mucosal offensive acid-pepsin secretion and defensive factors like mucin secretion, mucosal cell shedding, cell proliferation and antioxidant activity in rats. BME 20 mg/kg showed no effect on acid-pepsin secretion, increased mucin secretion, while it decreased cell shedding with no effect on cell proliferation. BME showed significant antioxidant effect per se and in stressed animals. Thus, the gastric prophylactic and curative effects of BME may be due to its predominant effect on mucosal defensive factors.     

Collagen type I fibril packing in vivo and in vitro

Reviewed are works concerning the mechanisms of collagen (type I) fibril packing and the influence of macromolecular structure and physicochemical parameters of the medium on the process.     

Carboxylierungsreaktionen in Agaricus bisporus III. Pyruvat und Phosphoenolpyruvat als CO2-Acceptoren

Zusammenfassung Zellfreie Extrakte aus Agaricus bisporus bilden Malat, Fumarat und Aspartat einerseits aus Pyruvat und CO₂ in Gegenwart von Mn²⁺ und andererseits aus Phosphoenolpyruvat und CO₂ in Gegenwart von Mg²⁺.Die Carboxylierung von Pyruvat wird durch ATP und NADPH₂ deutlich gefördert, ist aber unabhängig von der Anwesenheit von CoA-Estern. Die Reaktion erfährt durch pCMB, Oxalat und Avidin eine Hemmung.Die Carboxylierung von Phosphoenolpyruvat wird durch ADP, nicht aber durch GDP und IDP gefördert.Aus den Ergebnissen wird geschlossen, daß bei der Carboxylierung von Pyruvat sowohl Pyruvatcarboxylase als auch Malatenzym wirksam sind, während für die Oxalacetatsynthese aus Phosphoenolpyruvat PEP-Carboxykinase verantwortlich ist.Die Bedeutung der drei Enzyme im Zusammenhang mit der Ernährung des Kulturchampignons aus dem natürlichen Substrat, mit der Glucogenese und der Steuerung des Citronensäurecyclus wird diskutiert.

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Carboxylation reactions in Agaricus bisporus III. Pyruvate and phosphoenolpyruvate as CO₂-acceptors

Summary Cell-free extracts from Agaricus bisporus catalyze the synthesis of malate, fumarate and aspartate from pyruvate and CO₂ in the presence of Mn²⁺, and from phosphoenolpyruvate and CO₂ with Mg²⁺ (partially replaceable by Mn²⁺).The carboxylation of pyruvate is highly stimulated by ATP and NADPH₂, but is not affected by CoA-esters. The reaction is inhibited by pCMB, oxalate and avidin.The carboxylation of phosphoenolpyruvate is stimulated by ADP, but not by IDP and GDP.From cofactor-requirement and inhibitor studies it is concluded, that there are two enzymes, pyruvatecarboxylase and malic enzyme, which catalyze the carboxylation of pyruvate. Phosphoenolpyruvate carboxykinase is responsible for the CO₂-fixation into oxaloacetate.The significance of these three enzymes is discussed in connection with the nutrition of the fungus from its natural growth substrate and with the regulation of glycogenesis and the citric acid cycle.

     

Hyperosid,das Hauptflavonolglykosid von Davidia involucrata Baill.

Summary Hyperosid (quercetin-3-galactoside) was isolated from the bracts of the dove tree and identified by paper chromatography, melting point determinations, UV- and IR-spectroscopy. The yield of crystalline hyperosid was approximately 1% of the dry weight. It is the main glycoside of the bracts and also appears in the green leaves, but is absent in the bark, wood and fruit. Quercitrin (quercetin-3-rhamnoside) is also present, in minor amount. No other flavonol glycoside could be detected. The analytical results are discussed in relation to their possible taxonomic and physiological implications.     

Expression of a maize proteinase inhibitor gene is induced in response to wounding and fungal infection: systemic wound-response of a monocot gene

The isolation and characterization of cDNA and genomic clones encoding a proteinase inhibitor protein (MPI) in maize is reported. Accumulation of the MPI mRNA is induced in response to fungal infection in germinating maize embryos. The expression pattern of the MPI gene, in healthy and fungal infected maize tissues, was examined and compared with the expression pattern of a gene that codes for a pathogenesis-related protein (the PRms protein) from maize. These two genes are induced by fungal infection, however different signals trigger their activation. Accumulation of the proteinase inhibitor mRNA is more a consequence of the wound produced by the penetration and colonization of the host tissues by the pathogen, than the result of a direct molecular recognition of the pathogen by the plant, as is the case for the induction of the PRms gene. Wounding, or treatment with abscisic acid or methyl jasmonate, stimulate MPI mRNA accumulation, but not PRms mRNA accumulation. Local and systemic induction of the MPI gene expression in response to wounding occurs in maize plants. To the authors' knowledge, this is the first example of a gene from a monocotyledonous species that clearly shows a systemic wound response. The possible functional implications for the existence of different signal transduction pathways that simultaneously activate a battery of defense mechanisms against potential pathogens are discussed.     

Round-cell mutants of Salmonella typhimurium produced by transposition mutagenesis: Lethality of rodA and mre mutations

Summary Thirty-three insertions of transposon Tn10l6l7 into genes involved in the control of rod cell shape were isolated in Salmonella typhimurium by the characteristic glossy appearance of colonies composed of spherical cells. Genetic tests demonstrated that 25 (76%) were insertions in the rodA gene, 7 (21 %) were mre mutants, and 1 (3%) was a divD mutant. No insertion in the pbpA gene were found. Insertions in cell shape genes only appeared when strains displaying resistance to mecillinam (not caused by -lactamase production) were employed. Neither rodA nor mre insertions could be transduced to wild-type strains but they were normally accepted by mecillinam-resistant derivatives and by cya and crp mutants, which, unlike the corresponding Escherichia coli strains, did not display resistance to mecillinam. On the other hand, the divD insertion could be efficiently transduced to any strain. It is concluded that the rodA, mre, and divD genes are involved in the control of rod cell shape but, in addition, the RodA and Mre products perform some function(s) that is essential for wild-type cells but dispensable for some mecillinam-resistant strains, and for cya and crp mutants.