World Journal of Microbiology and Biotechnology

, Volume 30, Issue 4, pp 1301–1313

Lindane degradation by Candida VITJzN04, a newly isolated yeast strain from contaminated soil: kinetic study, enzyme analysis and biodegradation pathway

Original Paper

DOI: 10.1007/s11274-013-1551-6

Cite this article as:
Salam, J.A. & Das, N. World J Microbiol Biotechnol (2014) 30: 1301. doi:10.1007/s11274-013-1551-6


A new yeast strain was isolated from sugarcane cultivation field which was able to utilize lindane as sole carbon source for growth in mineral medium. The yeast was identified and named as Candida sp. VITJzN04 based on a polyphasic approach using morphological, biochemical and 18S rDNA, D1/D2 and ITS sequence analysis. The isolated yeast strain efficiently degraded 600 mg L−1 of lindane within 6 days in mineral medium under the optimal conditions (pH 7; temperature 30 °C and inoculum dosage 0.06 g L−1) with the least half-life of 1.17 days and degradation constant of 0.588 per day. Lindane degradation was tested with various kinetic models and results revealed that the reaction could be described best by first-order and pseudo first-order models. In addition, involvement of the enzymes viz. dechlorinase, dehalogenase, dichlorohydroquinone reductive dechlorinase, lignin peroxidase and manganese peroxidase was noted during lindane degradation. Addition of H2O2 in the mineral medium showed 32 % enhancement of lindane degradation within 3 days. Based on the metabolites identified by GC–MS and FTIR analysis, sequential process of lindane degradation by Candida VITJzN04 was proposed. To the best of our knowledge, this is the first report of isolation and characterization of lindane-degrading Candida sp. and elucidation of enzyme systems during the degradation process.


Candida Enzymes Kinetics Lindane Pathway 

Supplementary material

11274_2013_1551_MOESM1_ESM.doc (66 kb)
Supplementary material 1 (DOC 66 kb)

Copyright information

© Springer Science+Business Media Dordrecht 2013

Authors and Affiliations

  1. 1.Bioremediation Lab, Environmental Biotechnology Division, School of Biosciences and TechnologyVIT UniversityVelloreIndia

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