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From another study that mainly focused on the isolation of Candida albicans and
other clinically significant yeasts , the method used in the isolation of fungi made use of
Sabourauds Dextrose Agar (SDA) and Brain Heart Infusion Agar added with 5% Sheep
Blood (BHIA) plates. The cultured fungi inoculated on the agar plates were incubated at
30C and examined at 10 days for any observable yeast growth. Significant fungal
growth observed during routine bacteriological cultures whether from the SDA or BHIA
plates were identified using the conventional method of criteria in regards to their growth
and colonial morphology. For the confirmation and identification of Candida spp, the
VITEK2 Automated System was used. (Hamid et. Al, 2014)
R: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4362108/
R: http://www.agriculturejournals.cz/publicFiles/84781.pdf
Another also tested for the antioxidant activity of extracts obtained from white
and colored peas (Pisum sativum). The seed coats were cracked to separate from their
cotyledons, they were then sieved and cleaned manually. The seed coats were stored
inside an airtight container for analysis. Before subjecting the pure seed coats to a 12-
hour Soxhlet extraction with hexane, they were finely grounded. ( Troszynska et al,
2002)
R: http://agriculturejournals.cz/publicFiles/50862.pdf
The experiment by Gibbs and Horecker utilized pea roots and leaves
approximately 11 to 13 days old. The research requires the use of homogenized 120
grams of washed pea roots and 1200 mL acetone at -10C, filtered Pea Root Acetone
Powder which was subjected to a blender and filtered by suction.
The experiment also utilized pea leaf extracts through grinding 120 grams of
leaves, separated from their stems, together with same equivalents of acid-washed,
cold sand and 20ml of cold 0.25 M KHCO3. The preparation of the leaf extracts were
carried out at 0-4C. ( Gibbs et al, 1954)
R: https://www.ncbi.nlm.nih.gov/pubmed/13174590
The study made by Mauch, Hadwiger and Boller utilized carefully-split in half,
2cm long immature pea pods. The pea pods were grounded in liquid nitrogen and
homogenized in 0.1 M sodium citrate buffer, pH 5.0, at a ratio of 1:2 (w/v) thru the
conventional method using mortar and pestle. The solution was centrifuged (10 min,
l0,0Q0g), and the supernatant was used as the preparation to be used. (Mauch et al,
1983)
R: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1064341/
In another study also made by Mauch, Hadwiger and Boller used freshly
harvested immature pea pods (about 4 d after anthesis, 220 + 50 mg fresh weight) were
carefully split in half. The pea pods were grounded in liquid nitrogen with the use of
mortar and pestle. The product was extracted with cold 0.1 M Tris-HCl (pH 7.5),
containing 1 mM phenylmethylsulfonyl fluoride. The precipitates were further removed
by centrifugation at 20,000g for 20 minute. in the experiment, processes were carried
out on ice or at 4C in a cold room. ( Mauch et al, 1988)
R: https://www.ncbi.nlm.nih.gov/pubmed/16666142
R: https://www.ncbi.nlm.nih.gov/pubmed/13174550
The study by Greenberg and Galston utilized immature buds of peas, consisting
mainly of unexpanded leaflets, then stored in a beaker with crushed ice. The pea buds
were crushed with ignited sand and a minute volume of phosphate buffer with a ph of 7,
using the conventional method of mortar and pestle that had been pre-cooled at -15C.
The product was then subjected to centrifugation near 0C at 24000 x g for 30 minutes
to an hour. (Greenberg and Galston, 1959)
R: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC541239/