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Titolo:
Oxoid CO2 Gen (TM) atmosphere generation system for growth of capnophilic bacteria: an evaluation
Autore:
Turner, A; Hart, IT;
Indirizzi:
Russells Hall Hosp, Dept Microbiol, Dudley DY1 2HQ, W Midlands, England Russells Hall Hosp Dudley W Midlands England DY1 2HQ W Midlands, England Oxoid Ltd, Basingstoke RG24 8PW, Hants, England Oxoid Ltd Basingstoke Hants England RG24 8PW oke RG24 8PW, Hants, England
Titolo Testata:
BRITISH JOURNAL OF BIOMEDICAL SCIENCE
fascicolo: 3, volume: 56, anno: 1999,
pagine: 182 - 187
SICI:
0967-4845(1999)56:3<182:OCG(AG>2.0.ZU;2-O
Fonte:
ISI
Lingua:
ENG
Keywords:
bacteriological techniques; carbon dioxide; evaluation studies; growth substances;
Tipo documento:
Article
Natura:
Periodico
Settore Disciplinare:
Life Sciences
Citazioni:
14
Recensione:
Indirizzi per estratti:
Indirizzo: Turner, A Russells Hall Hosp, Dept Microbiol, Dudley DY1 2HQ, W Midlands, England Russells Hall Hosp Dudley W Midlands England DY1 2HQ s, England
Citazione:
A. Turner e I.T. Hart, "Oxoid CO2 Gen (TM) atmosphere generation system for growth of capnophilic bacteria: an evaluation", BR J BIOMED, 56(3), 1999, pp. 182-187

Abstract

The Oxoid CO2 Gen(TM) system is compared with BBL(R) GasPak(R) and a carbon dioxide (CO2) incubator to evaluate its ability to support and enhance the growth of capnophilic bacteria. Clinical samples (n = 109) from various anatomical sites and 23 spiked samples are evaluated. The criteria used to compare the systems include amount of growth, colony size, colony morphologyand haemolysis. Isolation rates, amounts of growth and morphology were similar in each system, but colony diameter was significantly larger in the jar-based systems. Significantly larger colonies grew in CO2 Gen(TM) than in BBL(R) GasPak(R). alpha-Haemolytic zones n ere significantly larger in jar-based systems than in the CO2 incubator, and significantly larger in CO2 Gen(TM) than in BBL(R) GasPak". beta-haemolytic zones were significantly larger in CO2 Gen(TM) than in the CO2 incubator. The CO2 Gen(TM) system appearsto be an excellent alternative to established methods for generating an environment for capnophilic incubation.

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Documento generato il 29/03/20 alle ore 09:06:26