1992
DOI: 10.1007/bf01198765
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Some universal media for the isolation, growth and purity checking of a broad spectrum of microorganisms

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1993
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Cited by 7 publications
(3 citation statements)
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“…AYM agar medium, comprising yeast extract, mannitol, agar‐agar, and essential nutrients, were prepared and autoclaved for sterilization. The nodule tissues were inoculated onto AYM agar plates, and following an incubation period, individual bacterial colonies were developed (Malik, 1992 ), using Congo red , whereby only rhizobia were morphologically identified from other microorganisms.…”
Section: Methodsmentioning
confidence: 99%
“…AYM agar medium, comprising yeast extract, mannitol, agar‐agar, and essential nutrients, were prepared and autoclaved for sterilization. The nodule tissues were inoculated onto AYM agar plates, and following an incubation period, individual bacterial colonies were developed (Malik, 1992 ), using Congo red , whereby only rhizobia were morphologically identified from other microorganisms.…”
Section: Methodsmentioning
confidence: 99%
“…Cance, 1968). Strains were conserved by regular subcultures under sterile mineral oil and refrigeration (5°C-10°C), as described by Malik (1992).…”
Section: Methodsmentioning
confidence: 99%
“…A pre-culture was prepared by inoculating a single colony in 10 ml of peptone medium consisting of (gl -1 ) peptone 30, yeast extract 10 and NaCl 5 (pH 7.0) and inoculated on a rotary shaker (240 rpm) for 24 h. The numbers of aerobic, heterotrophic, chemolithoautotrophic bacteria were determined on nutrient agar media for the isolation, growth and purification of microorganisms (Malik, 1992). Selective media with (NH4)2SO4 or Na NO2 were used in order to determine the most probable number of nitrite and nitrate bacteria respectively and peptonated water was used for ammonifying bacteria (Pochon, 1954;Gerhardt et al, 1994).…”
Section: Cultivation Mediamentioning
confidence: 99%