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Research Paper

Rapid development of xylanase assay conditions using Taguchi methodology

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Pages 424-431 | Received 29 Mar 2016, Accepted 13 Apr 2016, Published online: 19 Jul 2016
 

ABSTRACT

The present investigation is mainly concerned with the rapid development of extracellular xylanase assay conditions by using Taguchi methodology. The extracellular xylanase was produced from Aspergillus niger (KP874102.1), a new strain isolated from a soil sample of the Baramura forest, Tripura West, India. Four physical parameters including temperature, pH, buffer concentration and incubation time were considered as key factors for xylanase activity and were optimized using Taguchi robust design methodology for enhanced xylanase activity. The main effect, interaction effects and optimal levels of the process factors were determined using signal-to-noise (S/N) ratio. The Taguchi method recommends the use of S/N ratio to measure quality characteristics. Based on analysis of the S/N ratio, optimal levels of the process factors were determined. Analysis of variance (ANOVA) was performed to evaluate statistically significant process factors. ANOVA results showed that temperature contributed the maximum impact (62.58%) on xylanase activity, followed by pH (22.69%), buffer concentration (9.55%) and incubation time (5.16%). Predicted results showed that enhanced xylanase activity (81.47%) can be achieved with pH 2, temperature 50°C, buffer concentration 50 Mm and incubation time 10 min.

Disclosure of Potential Conflicts of Interest

No potential conflicts of interest were disclosed.

Funding

This material is based on work supported by the National Institute of Technology, Agartala, India. The authors would like to acknowledge the National Institute of Technology, Agartala, Ministry of Human Resource and Development, Government of India for Fellowship 0000-0003-4637-991X.

Compliance with Ethical Standards

This article does not contain any studies with human participants or animals performed by any of the authors.

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