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Studying some of the optimal conditionals for the best bacterial isolates from soil and its effects on their growth rates
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Abstract<p>The current study aimed to use some bacterial isolates from the local soil of Baghdad city by study the effects of temperature, pH and incubation period on the growth rates of isolated bacteria and choose the optimal conditions for their diversity and for understanding bacterial growth and their requirements for survival and proliferation. This information can be applied to obtain their high growth rate for use in various fields such as agriculture, medicine and environmental sciences in the future. And it used to assess the degree of variation in across bacteria species in pH, temperature and incubation period. A number of local bacterial isolates as <italic>Enterobacter cloacae</italic>, <italic>Aeromonas hydrophila, Pantoea spp.</italic>, <italic>Pseudomonas mendocina</italic> and <italic>Serratia fonticola</italic> identified in this study. The growth rate of the bacterial isolates was tested by growing each bacterial isolate in a different range of pH (4, 7 and 10) and under the influence of several temperatures (52, 35 and 50) and within different incubation periods (24, 48 and 72) hours The optimal conditions were determined by measuring the optical density (absorbance) at a wavelength of 600 nm, which represents bacterial growth. The optimal conditions for <italic>E. cloacae</italic> were determined to be a pH of 10 and a temperature of 35°C after a 72hour incubation period. Similarly, <italic>A. hydrophila</italic> exhibited optimal growth at a pH of 7 and a temperature of 35°C after a 72hour incubation period. <italic>Pantoea</italic> spp. demonstrated optimal growth at a pH of 7 and a temperature of 25°C after a 24hour incubation period. <italic>P. mendocina</italic> displayed optimal growth at a pH of 7 and a temperature of 25°C after a 72hour incubation period. Lastly, <italic>S. fonticola</italic> exhibited optimal growth at a pH of 7 and a temperature of 50°C after a 72hour incubation period.</p>
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Publication Date
Thu Nov 19 2020
Journal Name
Indonesian Journal Of Chemistry
Determination of Eugenol in Personal-Care Products by Dispersive Liquid-Liquid Microextraction Followed by Spectrophotometry Using &lt;i&gt;p&lt;/i&gt;-Amino-&lt;i&gt;N,N&lt;/i&gt;-dimethylaniline as a Derivatizing Agent
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Two simple methods for the determination of eugenol were developed. The first depends on the oxidative coupling of eugenol with p-amino-N,N-dimethylaniline (PADA) in the presence of K3[Fe(CN)6]. A linear regression calibration plot for eugenol was constructed at 600 nm, within a concentration range of 0.25-2.50 μg.mL–1 and a correlation coefficient (r) value of 0.9988. The limits of detection (LOD) and quantitation (LOQ) were 0.086 and 0.284 μg.mL–1, respectively. The second method is based on the dispersive liquid-liquid microextraction of the derivatized oxidative coupling product of eugenol with PADA. Under the optimized extraction procedure, the extracted colored product was determined spectrophotometrically at 618 nm. A l

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