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Rapid api kits

Manufactured by bioMérieux
Sourced in France

Rapid API kits are a line of laboratory test kits produced by bioMérieux. The kits are designed to provide rapid identification and quantification of specific biological agents or analytes in various sample types. The core function of these kits is to enable efficient and accurate testing in clinical, food, or environmental settings.

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2 protocols using rapid api kits

1

Comprehensive Microbial Characterization of Organic Fertilizer

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The standard method for total aerobic plate count was adopted in analyzing the aerobic bacteria in the fermenting material; inoculum, digestate, and solid organic fertilizer in this study employing nutrient agar, eosin methylene blue (EMB) agar, peptone water, and MacConkey agar. All samples were collected aseptically and in triplicates while presumptive isolates were characterized by phenotypic methods and the probable ones further identified using appropriate rapid API kits (BioMerieux, France) as previously reported28 (link)–33 (link).
To characterize the anaerobic bacteria, samples were initially cultured on two enriched media (Reinforced Clostridia medium and blood agar) in anaerobic chambers at 37º C between 5 and 7 days. This was meant to detect members of the Clostridia and other facultative anaerobes in the samples. After this, Brain Heart Infusion agar was employed in fully growing developed colonies followed by counting and recording46 (link). The phenotypic features of the presumptive isolates were determined after which appropriate rapid API kits were used for their final confirmation47 (link). For fungal evaluation, samples were cultured on Potato dextrose agar and grown for 5–7 days before identification by hypha and spore morphology and those of the fruiting bodies48 .
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2

Characterization of Aerobic and Anaerobic Bacteria in Anaerobic Digestion

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Aerobic bacteria involved at every stage of the AD were isolated and characterized following standard methods with specific media. Biochemical and phenotypic methods were used in the identification and suspected candidates were confirmed with the aid of appropriate rapid API kits (BioMerieux). Fungal organisms were isolated by culturing samples on Potato dextrose agar (PDA) and the dynamics of fungal hyphae, structures/morphology of cell spores and the nature of their fruiting bodies were employed in their identification. Facultative Clostridium species and other anaerobic acidogens were isolated anaerobically using two important media (Reinforced Clostridia medium and blood agar) at temperature of 37 °C for approximately one week. Biochemical procedures were followed in the preliminary characterization and the suspected isolates were identified using appropriate rapid API kits as reported (Ayandiran and Dahunsi, 2017) . All analyses were carried out weekly in triplicates in the Microbiology laboratory of Biological Sciences Department, Covenant University, Ota, Nigeria.
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