2012
DOI: 10.1007/s13213-012-0538-0
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Exoglucanase production by Aspergillus niger grown on wheat bran

Abstract: β-Exoglucanase production on the lignocellulosic material, wheat bran, by Aspergillus niger under solid state fermentation (SSF) on a laboratory scale was investigated. Different fermentation parameters, such as moisture content, initial pH, temperature, depth of the substrate, and inoculum size on exoglucanase production were optimized. Moisture content of 40 %, pH of 7.0, substrate depth of 1.0 cm, inoculum size of 2×10 6 spores/g of wheat bran, and temperature at 30 °C were optimal for maximum production of… Show more

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Cited by 16 publications
(2 citation statements)
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“…However, the exact optimal inoculum size varies with specific conditions (strains, inoculation strategies, and so on). Subhosh Chandra et al optimized the inoculum size of 2 × 10 6 spores/g for maximum metabolites using WB . With the increase of inoculation amount, the target fungi inhibit the survival of other microorganisms to become the dominant colony in the matrix, thus shortening the delay period and further accelerating the synthesis and secretion of specific enzymes.…”
Section: Resultsmentioning
confidence: 99%
“…However, the exact optimal inoculum size varies with specific conditions (strains, inoculation strategies, and so on). Subhosh Chandra et al optimized the inoculum size of 2 × 10 6 spores/g for maximum metabolites using WB . With the increase of inoculation amount, the target fungi inhibit the survival of other microorganisms to become the dominant colony in the matrix, thus shortening the delay period and further accelerating the synthesis and secretion of specific enzymes.…”
Section: Resultsmentioning
confidence: 99%
“…(2) Exoglucanase Activity. Exoglucanase activity as flter paperase (FPase) activity in the hydrolyzate was determined according to the method described by Chandra and Reddy [52] as follows: 1 mL of the hydrolyzate (i.e., the cocktail enzymes) was mixed with 2 mL of 0.1 M citrate bufer pH 4.8 containing 0.05 g of flter paper (Whatman no.1). Te tube was incubated at 50 °C for 1 h. Te liberated TRSs were measured by the DNSA method, as described before, at λ 540 nm .…”
Section: (Hemi) Cellulolytic Enzymes Assaysmentioning
confidence: 99%