South Asian Journal of Research in Microbiology
https://journalsajrm.com/index.php/SAJRM
<p style="text-align: justify;"><strong>South Asian Journal of Research in Microbiology</strong> <strong>(ISSN: <a href="https://nsl.niscpr.res.in/ISSNPROCESS/issnassignedinfo.jsp">2582-1989</a>) </strong>aims to publish high quality papers (<a href="https://journalsajrm.com/index.php/SAJRM/general-guideline-for-authors">Click here for Types of paper</a>) in all aspects of Microbiology. By not excluding papers based on novelty, this journal facilitates the research and wishes to publish papers as long as they are technically correct and scientifically motivated. The journal also encourages the submission of useful reports of negative results. This is a quality controlled, OPEN peer-reviewed, open-access INTERNATIONAL journal.</p>en-US[email protected] (South Asian Journal of Research in Microbiology)[email protected] (South Asian Journal of Research in Microbiology)Thu, 01 Oct 2026 12:16:57 +0000OJS 3.3.0.21http://blogs.law.harvard.edu/tech/rss60Antimicrobial Susceptibility and Biofilm-Forming Ability of Airborne Bacteria Isolated from Selected Livestock Farms and Abattoirs in Port Harcourt, Nigeria
https://journalsajrm.com/index.php/SAJRM/article/view/532
<p><strong>Background:</strong> Airborne microbial contamination in livestock farms and abattoirs poses significant public health, animal welfare, and food safety risks because of high animal density, inadequate ventilation, and processing activities that generate bioaerosols.</p> <p><strong>Materials and Methods:</strong> This study assessed the distribution, diversity, antibiotic susceptibility, and biofilm-forming potential of airborne microorganisms in six livestock-related environments in Port Harcourt, Nigeria: Piggery Farm, Goat Farm, Cattle Farm, Rumuokoro Abattoir, Eagle Island Abattoir, and Tech Farm Abattoir. Air samples were collected by passive sedimentation using exposed Nutrient Agar, MacConkey Agar, and Sabouraud Dextrose Agar plates placed in areas of high animal activity, waste disposal, and slaughter-processing operations for 10 minutes. The plates were incubated at 37°C for 24–72 hours. Bacterial isolates were identified using colonial morphology, Gram staining, and standard biochemical tests, while fungal isolates were identified based on their macroscopic and microscopic characteristics. Antibiotic susceptibility was determined using the Kirby–Bauer disc diffusion method, and microbial load was expressed as colony-forming units per minute per square metre (CFU/min·m²).</p> <p><strong> </strong></p> <p><strong>Results:</strong> Rumuokoro Abattoir recorded the highest microbial load, with total heterotrophic bacterial count, total coliform count, and total fungal count of 36.38 ± 15.91, 38.60 ± 18.24, and 5.10 ± 0.28 CFU/min·m², respectively. A total of 24 bacterial isolates belonging to nine genera were identified, comprising <em>Staphylococcus</em> spp., <em>Bacillus </em>spp., <em>Lederbergia</em> sp., <em>Micrococcus</em> sp., <em>Serratia</em> spp., <em>Arsenophonus </em>sp., <em>Cronobacter</em> sp., <em>Klebsiella </em>spp., and <em>Citrobacter</em> spp. <em>Staphylococcus </em>spp. showed the highest occurrence (29.2%), followed by <em>Bacillus</em> spp. (20.8%). Five fungal taxa were recovered: <em>Penicillium</em> sp., <em>Mucor</em> sp., <em>Aspergillus niger,</em> <em>Trichophyton </em>sp., and <em>Fusarium </em>sp. Antibiotic susceptibility testing showed that most <em>Bacillus </em>spp. and <em>Staphylococcus</em> spp. were resistant to rifampicin, ceftazidime, azithromycin, and cefuroxime, with only limited susceptibility to gentamicin and levofloxacin. Among the Gram-negative isolates, <em>Serratia</em> spp. and <em>Citrobacter</em> spp. were resistant to all antibiotics tested, whereas <em>Klebsiella</em> spp. and<em> Cronobacter</em> spp. exhibited susceptibility to selected antibiotics with some intermediate responses. Biofilm production was detected in <em>Klebsiella</em> spp., <em>Citrobacter </em>spp., and <em>Bacillus</em> spp.</p> <p><strong>Conclusion:</strong> The livestock farms and abattoirs in the study areas harbours diverse airborne microorganisms, including antibiotic-resistant and biofilm-forming bacterial species, with abattoirs exhibiting the highest microbial contamination.</p>Owhonka Aleruchi, Berembo Beremboba Teleme, Tamunotonye Angel Halliday
Copyright (c) 2026 Author(s). The licensee is the journal publisher. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
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https://journalsajrm.com/index.php/SAJRM/article/view/532Thu, 01 Oct 2026 00:00:00 +0000Influence of Chemical Preservatives on Quality Attributes of Kunu-zaki-a Nigerian Traditional Fermented Cereal Beverage
https://journalsajrm.com/index.php/SAJRM/article/view/533
<p><em>Kunu-zaki</em> is a traditional fermented cereal beverage valued for its accessibility but susceptible to microbial spoilage during storage. This study examined the effects of sodium benzoate (E211), potassium sorbate (E202) and their combination on the physicochemical, microbiological and sensory characteristics of <em>kunu-zaki</em>. Laboratory-prepared beverage samples were allocated to four treatments: sodium benzoate at 0.1% (A), potassium sorbate at 0.1% (B), a combination of both preservatives at 0.05% each (C) and an untreated control (D). Samples were assessed on days 0, 2 and 4 for pH, proximate composition and microbial counts; sensory characteristics were evaluated by 20 panellists using a five-point hedonic scale. The control pH declined from 5.8 to 3.3 during storage, whereas the corresponding day-4 pH values for treatments A, B and C were 5.2, 5.0 and 5.3, respectively. The day-4 total viable counts were 1.0 × 10⁶, 1.0 × 10⁶, 5.0 × 10⁵ and 8.0 × 10⁶ CFU/mL for A, B, C and D, respectively. No yeast/mould count was recorded for treatment C on day 4, whereas the control had a count of 5.0 × 10⁷ CFU/mL. Overall sensory acceptability scores were 3.4, 4.0, 3.8 and 1.6 for samples A–D, respectively. These findings suggest that the preservatives influenced selected quality indicators during four days of storage, although remaining microbial counts preclude conclusions about product safety.</p>Isaac Ayanniran Adesokan, Ekanola Yetunde Aderemi, Bolarinwa Oluwatoyin Olubisi, Adekola Abdulwasiu, Adeniji Abiodun Abiola
Copyright (c) 2026 Author(s). The licensee is the journal publisher. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
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https://journalsajrm.com/index.php/SAJRM/article/view/533Thu, 15 Oct 2026 00:00:00 +0000An Alternative Approach to Extraction of Enzymes from Saccharomyces cerevisiae Using Snail Slime and Hydraulic Pressure
https://journalsajrm.com/index.php/SAJRM/article/view/534
<p>The need for environmentally sustainable enzyme extraction methods has increased due to the growing demand for industrial bioprocesses. In this study, slime from <em>Achatina achatina</em> combined with syringe-needle hydraulic pressure was used to lyse <em>Saccharomyces cerevisiae</em> cells and recover a crude intracellular enzyme extract. Cells from a stock of a highly ethanol-tolerant strain of <em>Saccharomyces cerevisiae</em> isolated from palm wine were cultured on modified Potato Dextrose Agar (PDA) supplemented with 0.5% potassium phosphate (K<sub>2</sub>HPO<sub>4</sub>) and incubated in a candle jar for 3 days. A standardised yeast suspension was prepared from the resulting colonies. Equal volumes of <em>Saccharomyces cerevisiae</em> suspension and snail slime (1:1 ratio) were mixed and left to stand for 1 hour. The mixture was repeatedly homogenized by hydraulic pressure through repeated syringe-needle (340 µm) passage for three rounds. The lysed cell suspension was filtered through a 0.45 µm membrane filter to obtain a crude enzyme extract. The extract was evaluated for its ethanol production potential using glucose solutions at different concentrations (1%, 2.5%, 5%, 7.5%, and 10% v/v). The results showed that no ethanol was detected at 1% glucose, while ethanol yield increased progressively with increasing glucose concentration, from 0.27% v/v at 2.5% glucose concentration to 0.37% v/v at 10% glucose concentration. The absence of ethanol at 1% glucose likely reflected insufficient carbon substrate, whereas higher glucose levels supported measurable enzymatic activity. These findings indicated that snail slime-assisted lysis combined with hydraulic pressure effectively disrupted yeast cells and yielded active enzyme extracts capable of ethanol production. This approach offers a simple, eco-friendly, and low-cost alternative to conventional crude enzyme extraction techniques and may have potential applications in industrial biotechnology and cell-free ethanol production systems.</p>Joy Uchechukwu Ezeonyilimba, Lekiah Pedro Peekate, Lawrence O. Amadi, Salome Ibietela Douglas
Copyright (c) 2026 Author(s). The licensee is the journal publisher. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
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https://journalsajrm.com/index.php/SAJRM/article/view/534Sat, 17 Oct 2026 00:00:00 +0000