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Xylanase production by Penicillium chrysogenum (PCL501) fermented on cellulosic wastes

TLDR
Out of the three agro-wastes used in this study, wheat bran holds the greatest promise for cost-effective production of the xylanase enzyme, as the carbon source is the highest inducer of the enzyme in the fungus.
Abstract
Xylanase production by Penicillium chrysogenum PCL501, newly isolated from wood-wastes, was monitored at 24 h intervals for a period 168 h in media containing four different carbon sources (oatspelt xylan, wheat bran, sawdust, and sugarcane pulp). The highest xylanase activity of 6.47 Units mL-1 was obtained at 96 h in media containing wheat bran whereas media containing sugarcane pulp gave a peak value of 1.39 Units mL-1 at 144 h. Sawdust and xylan gave a peak xylanase activity of 1.35 and 0.79 Units mL-1 respectively at 120 h. Maximum protein released in xylan-containing media was 0.38 mg mL-1. Higher protein yield was obtained in media containing the agro-wastes, with wheat bran giving the highest value of 1.14 mg mL-1. The maximum specific xylanase activities were 2.59, 8.52, 16.06, and 9.36 Units mg Protein -1 for sawdust, sugarcane pulp, wheat bran and xylan respectively. Out of the three agro-wastes used in this study, wheat bran holds the greatest promise for cost-effective production of the xylanase enzyme. The carbon source is the highest inducer of the enzyme in the fungus.

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Citations
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Potential of Penicillium Species in the Bioremediation Field

TL;DR: Several studies conducted with different strains of imperfecti fungi, Penicillium spp.
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Production, purification, and characterization of a major Penicillium glabrum xylanase using Brewer's spent grain as substrate.

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One-factor-at-a-time (OFAT) optimization of xylanase production from Trichoderma viride-IR05 in solid-state fermentation

TL;DR: In this paper, the authors dealt with the production of enzyme xylanase by solid substrate fermentation using Trichoderma viride -IR05 and found that sugarcane bagasse was the best substrate for enzyme synthesis.
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Cost-Effective Production and Optimization of Alkaline Xylanase by Indigenous Bacillus mojavensis AG137 Fermented on Agricultural Waste

TL;DR: Produced xylanase was introduced as an alkaline-active and stable one, displaying suitable thermostability feature, confirmed by HPLC analysis, and all xylan enzyme properties highlight its promising uses in industrial scale.
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Xylanases: An Overview

TL;DR: Its distribution, structural aspects and industria l/ biotechnological applications are reviewed and studies related to cloning of the gene encoding endo-1,4-�≤ -xylanase with the objectives of overproducing the enzyme and altering its properties to suit commercial applications are discussed.
References
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Journal Article

Protein Measurement with the Folin Phenol Reagent

TL;DR: Procedures are described for measuring protein in solution or after precipitation with acids or other agents, and for the determination of as little as 0.2 gamma of protein.
Journal ArticleDOI

Utilization of banana waste for the production of lignolytic and cellulolytic enzymes by solid substrate fermentation using two Pleurotus species (P. ostreatus and P. sajor-caju)

TL;DR: Leaf biomass was found to be a more suitable substrate compared to pseudostems for enzyme production and very low levels of cellulolytic enzyme activities were detected compared to lignin degrading enzymes by both the organisms.
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