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J Bata

Publications and source records attributed to J Bata.

21 records · Page 2Linked to original sources

Glycoside hydrolase production by an anaerobic rumen fungus Caecomyces communis.

The ruminal fungus Caecomyces communis was grown anaerobically either in a discontinuous cultivation system or in a fermentor with daily withdrawal and addition of fresh medium. Lowe and Orpin media were tested. The best culture conditions for glycoside hydrolase production were obtained in Lowe medium with daily fresh medium addition, whereas the Orpin medium with ruminal fluid was favourable to fungal growth and to the enzyme export process. Among glycoside hydrolases assessed in both culture fluid and cellular homogenate, beta-D-fucosidase activity was preponderant. Most studied enzymes were mainly associated with cells (from 50% to 99%). Glycoside hydrolase activities were constitutive, but their level was regulated by a carbon source. beta-D-fucosidase and beta-D-xylosidase activity production was activated by the association of glucose plus cellobiose, whereas beta-D-glucosidase activity production was stimulated by cellobiose alone. Enzyme release could be favoured by glucose alone or by Ray grass hay added to glucose plus cellobiose.

Anaerobiosis↗

[Alpha 1-antitrypsin/lymphocyte interactions: cytofluorometry study].

Purified alpha 1-antitrypsin (alpha 1AT) was previously shown to prevent primary antibody response and lymphocyte DNA synthesis. We have reported that radiolabelled alpha 1-AT could bind to human lymphocytes and inhibit surface proteolytic activity. However, the radiolabelling method brings no information on the eventual heterogeneity of alpha 1AT distribution among the population nor on the presence of alpha 1AT on untreated lymphocytes. In this report, we have investigated these two points using indirect fluorescence followed by flow cytofluorometric analysis. The presence of alpha 1AT was revealed on a variable percentage of untreated peripheral blood and tonsillar lymphocytes. The incubation of cells with additional alpha 1AT induced an increase of the percentages of fluorescent lymphocytes. This binding was specific and could be inhibited by pretreatment with the protease inhibitor tosyl-L-phenylalanine-chloromethyl-ketone (TPCK) (2 X 10(-5)M). Furthermore, TPCK and EDTA (3 mM) could displace alpha 1AT initially bound to the lymphocyte surface.

Cell Separation↗