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Pseudomonas isolation agar

Manufactured by HiMedia
Sourced in India

Pseudomonas isolation agar is a selective and differential culture medium used for the isolation and identification of Pseudomonas species from environmental and clinical samples. It contains ingredients that inhibit the growth of most other bacteria, allowing Pseudomonas species to grow more readily.

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4 protocols using pseudomonas isolation agar

1

Comprehensive Microbial Characterization Protocol

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Culture, morphophysiology and biochemical characters of the microbial isolates were studied following standard methods (Ventosa et al., 1998 (link)). The isolates were checked for colony characters, motility, shape/size of the organism, and Gram and endospore staining. Biochemical tests, hydrolysis to carbohydrates and its metabolism as well as tolerance to NaCl were performed. Colony characters of isolates were observed on HiCrome Bacillus agar, rapid HiEnterococci agar, rapid HiColiform agar, Enterococcus confirmatory agar, Kligler iron agar, Chapman stone agar, Pikovskaya's agar, KG agar, Pseudomonas isolation agar, Hifluoro Pseudomonas agar base phenylalanine agar, triple sugar-iron agar, coagulase mannitol agar and HiCrome staph agar base for characterization of the bacteria (HiMedia Pvt Ltd, Mumbai).
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2

Analytical Characterization of Biochemical Compounds

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All chemicals used were of analytical grade. Thiobarbituric acid (TBA), trichloroacetic acid (TCA), 1,1,3,3-tetramethoxypropane, Brij-L23, tetramethylmurexide, and L-β-(3,4 dihydroxyphenyl) alanine (L-DOPA) were procured from Sigma Aldrich (St. Louis, MO, USA). Potassium carbonate and copper (II) sulfate were purchased from Thermo Fisher Scientific (Auckland, New Zealand). The microbial media (eosin methylene blue agar (EMB), Pseudomonas isolation agar (PIA), plate count agar (PCA), triple sugar iron agar, and Mueller–Hinton broth (MHB) were acquired from Himedia (Mumbai, India).
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3

Isolation of Fluorescent Pseudomonads from Drought-Prone Soils

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Rhizosphere adhering soil samples were collected from ten different locations of green gram cultivating areas of Jorhat district of Assam, located in 26.75°N and 94.22°E of North East India. Sampling sites were selected based on minimal annual precipitation, i.e mainly drought prone areas. Sampling was carried out during the month of October (vegetative growth phase) and February (reproductive growth phase), 2011–2012. Soils were clay loam in texture with pH of 3.5 to 4. The soil samples from each location were combined and passed through 0.2 cm sieve and preserved at 4°C until use. A total of 120 fluorescent pseudomonad colonies were obtained upon growth on King’s B agar (KB) and Pseudomonas isolation agar (Hi Media, Mumbai, India) medium by incubating at 30±2°C for 24 hours The isolates were stored in 20% glycerol stock at −80°C until use.
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4

Microbial Enumeration and Isolation

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All chemicals used were of analytical grade. Plate count agar was procured from Difco (Maryland, USA). Eosin methylene blue (EMP) agar, triple sugar iron agar, and Pseudomonas isolation agar were obtained from Himedia (Mumbai, India).
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