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Journal ArticleDOI

A rapid and easy method for the detection of microbial cellulases on agar plates using gram's iodine

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TLDR
This is the first report on the use of Gram’s iodine for the detection of cellulase production by microorganisms using plate assay, which is rapid and efficient and can be easily performed for screening large numbers of microbial cultures of both bacteria and fungi.
Abstract
Screening for cellulase-producing microorganisms is routinely done on carboxymethylcellulose (CMC) plates. The culture plates are flooded either with 1% hexadecyltrimethyl ammonium bromide or with 0.1% Congo red followed by 1 M NaCl. In both cases, it takes a minimum of 30 to 40 minutes to obtain the zone of hydrolysis after flooding, and the hydrolyzed area is not sharply discernible. An improved method is reported herein for the detection of extracellular cellulase production by microorganisms by way of plate assay. In this method, CMC plates were flooded with Gram’s iodine instead of the reagents just mentioned. Gram’s iodine formed a bluish-black complex with cellulose but not with hydrolyzed cellulose, giving a sharp and distinct zone around the cellulase-producing microbial colonies within 3 to 5 minutes. The new method is rapid and efficient; therefore, it can be easily performed for screening large numbers of microbial cultures of both bacteria and fungi. This is the first report on the use of Gram’s iodine for the detection of cellulase production by microorganisms using plate assay.

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Citations
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Journal ArticleDOI

Synergistic Effects of Cellulase-Producing Microorganisms for Future Bioconversion of Lignocellulosic Biomass

TL;DR: Findings of synergistic effects of microbial consortia could bring a future work to develop high efficient cellulase producing systems for further industry application.
Patent

Fast screening method for cellulase-yielding strain based on dyeing method

TL;DR: In this article, a fast screening method for a cellulase-yielding strain based on a dyeing method was proposed, which consisted of the following steps: culturing and dyeing screening, wherein culturing comprises selection and preparation of a culture medium and constant-temperature culture by employing the culture medium, and screening, namely weighing 5-10mL of a I2/KI aqueous solution with the mass percentage by concentration of 0.2-1.0%, adding the solution into a cultured slab where bacterial colonies grow fully, and lightly swinging the slab,

Eksplorasi Jamur Alkalotoleran dari Desa Sukolilo Barat, Kecamatan Labang, Kabupaten Bangkalan, Madura, Jawa Timur Helga Lusiana, MG Isworo Rukmi dan Budi Rahardjo

TL;DR: The result of amylolytic test showed Trichoderma longibrachiatum have the highest activity at pH 8, while Fusarium sp 2 (IMD-24) showed the highestactivity at pH 9.0, and Aspergillus flavus showed highest proteolytic activity a t pH 8.0.
Posted ContentDOI

Production,characterization and applications of cellulase from thermophilic Anoxybacillus and Bacillus

TL;DR: In this paper , four thermophilic bacteria were screened for thermostable cellulase production on the basis of clear zone formation with 1 % CMC and all the isolates gave maximum activity in presence of CMC upto range of 4.1-4.9 U/mL.
References
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Journal ArticleDOI

Cellulases and related enzymes in biotechnology

TL;DR: The present article is an overview of the biotechnological state-of-the-art for cellulases and related enzymes.
Journal ArticleDOI

The biological degradation of cellulose

TL;DR: The study of cellulolytic enzymes at the molecular level has revealed some of the features that contribute to their activity and an increasing number of three-dimensional structures are becoming available for cellulases and xylanases belonging to different families, which will provide paradigms for molecular modeling of related enzymes.
Journal ArticleDOI

The Properties of Fungal and Bacterial Cellulases with Comment on their Production and Application

TL;DR: Structure de la cellulose, sources et production d'enzymes cellulolytiques: regulation, secretion, mutation, mutation et clonage, multiplicite des enzymes.
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