1976
DOI: 10.1111/j.1365-2672.1976.tb04165.x
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The Application of Miniaturized Methods for the Characterization of Various Organisms Isolated from the Animal Gut

Abstract: Miniaturized methods for the characterization of streptococci, lactobacilli and aerobic Gram negative rods are described and the results obtained with 461 cultures from the calf rumen and quail gut tabulated. The methods afford a considerable saving in time and materials without concomitant loss of accuracy.

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Cited by 55 publications
(10 citation statements)
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“…The different isolates on the basis of characteristics of colony morphology (shape, surface and color), cell morphology (shape and size), phenotypic and lactobacillus specifi c biochemical features were investigated. Eight bacterial isolates were considered to belong to the genus lactobacillus based on morphological, cultural and biochemical characteristics [Jayne- Williams, 1976]. Representative 16S rDNA amplicons of each of the different profi les were selected for sequencing.…”
Section: Resultsmentioning
confidence: 99%
“…The different isolates on the basis of characteristics of colony morphology (shape, surface and color), cell morphology (shape and size), phenotypic and lactobacillus specifi c biochemical features were investigated. Eight bacterial isolates were considered to belong to the genus lactobacillus based on morphological, cultural and biochemical characteristics [Jayne- Williams, 1976]. Representative 16S rDNA amplicons of each of the different profi les were selected for sequencing.…”
Section: Resultsmentioning
confidence: 99%
“…Isolates were phenotypically assigned to the genus level on the basis of: cell morphology, Gram-positive and catalase-negative, according to the methods and criteria described by Sharpe (42) and Kandler and Weiss (26); CO 2 production from glucose in MRS broth containing inverted Durham tubes (32); hydrolysis of arginine, growth at 15 °C and 45 °C, tolerance to 20, 40, 65 g L -1 NaCl. The acid production from carbohydrates (fructose, glucose, mannitol, lactose, mannose, rhamnose, glycerol, arabinose, sorbose, dulcitol, amygdalin, melibiose, melezitose, starch, tagatose, arabitol, ribose, maltose, galactose, and xylose) was evaluated by using a miniaturized assay in microtiter plates, as described by Jayne-Williams (25). Ability to ferment carbohydrate substrates was studied, using the API 50 CHL system (BioMérieux, Lyon, France), following the manufacturer recommendations.…”
Section: Methodsmentioning
confidence: 99%
“…All isolates were grown in MRS broth at 30C for 24 h, purified by streaking on MRS agar and maintained in MRS broth plus 30% (w/v) glycerol (Merck) at –20C. The gram‐positive and catalase‐negative strains were subjected to the following physiological and biochemical tests: gas (CO 2 ) formation from glucose, arginine hydrolysis, growth in 8 and 10% NaCl, growth at 4, 10, 15, 37 and 45C, dextran production and fermentation of the following sugars: maltose, mannitol, melibiose, lactose, L‐arabinose, sucrose, raffinose, cellobiose, trehalose, ribose, sorbitol, D‐xylose and galactose according to Sharpe (1979) using the miniplate method described by Jayne‐Williams (1976). Sugar fermentation pattern was, also, determined using API 50 CHL (BioMerieux, Marcy l'Etoile, France), and the identification was performed by the computer program APILAB Plus (France).…”
Section: Methodsmentioning
confidence: 99%