1975
DOI: 10.1177/004051757504500511
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Amino-Acid Composition of Total Protein of Cotton

Abstract: The amino-acid composition of the total protein of cotton and primary wall of cotton have been determined after acid hydrolysis. Some amino acids (pro, thr, ile, phe, met, lys, his) not reported previously to be in cotton have been found. Cotton and primary wall of cotton contain free amino acids in addition to protein.

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Cited by 5 publications
(4 citation statements)
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“…Tripp and co-workers attributed most of this to protein. In addition to measuring the protein amino acids in the cotton fiber and primary wall, Wakelyn discovered free amino acids in cotton fiber and in primary wall preparations [50]. We have also detected nitrogenous compounds in methanol extracts of raw cotton lint [7].…”
Section: Resultsmentioning
confidence: 99%
“…Tripp and co-workers attributed most of this to protein. In addition to measuring the protein amino acids in the cotton fiber and primary wall, Wakelyn discovered free amino acids in cotton fiber and in primary wall preparations [50]. We have also detected nitrogenous compounds in methanol extracts of raw cotton lint [7].…”
Section: Resultsmentioning
confidence: 99%
“…Weight loss values obtained in these acid protease scouring are comparable to acid pectinase (0.31-4.0%), alkaline pectinase (1.5-3.8%) scouring as reported in the literature (Calafell & Garriga, 2004;Sahin & Gursoy, 2005;Traore & Diller, 2000). However, the weight loss values obtained in the protease scouring is much higher than the protein residues normally present in the unscoured samples (Wakelyn, 1975) that also suggest removal of other impurities like protopectin and waxy substances attached to the protein.…”
Section: Weight Lossmentioning
confidence: 83%
“…Fermentation was carried out, separately for both the sources, in a 250 mL Erlenmeyer's flask by transferring 10 mL of inoculum into 90 mL of fermentation medium and incubating at 37°C under shaking conditions. Samples were collected for 120 h at an interval of 12 h from both the cultures, centrifuged at 10,000 rpm for 15 min and the supernatant was used as enzyme source (Dahot, 1993;Wakelyn, 1975).…”
Section: Inoculum Preparationmentioning
confidence: 99%
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