Journal
ANNALS OF MICROBIOLOGY
Volume 62, Issue 3, Pages 1089-1098Publisher
SPRINGER
DOI: 10.1007/s13213-011-0350-2
Keywords
Antifungal activity; Chitosanase; Cyanobacteria; HPLC; q-RT PCR
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Funding
- AMAAS Network project on Microorganisms
- Indian Council of Agricultural Research (ICAR), New Delhi
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A novel antifungal chitosanase from Anabaena fertilissima, strain RPAN1, was characterized as a prelude to its use in biocontrol. The culture grown at 8:16 h L:D photoperiod showed highest chitosanase/antifungal activity under environmental and nutritional conditions of 43 mu M of P level, pH 9.0 and temperature of 27A degrees C. The transcriptional level of chitosanase encoding gene (cho) measured using quantitative real-time PCR (qRT-PCR) also indicated increased expression levels under the same optimized conditions. Under these conditions, cho encoding chitosanase was purified which exhibited a specific activity of 822 U/mg. The chitosanase activity measured using different substrates showed the highest activity against colloidal chitosan. HPLC profile of the products of enzyme activity with different chitosan oligosaccharides revealed the production of dimer units (GlcN)(2) or more, confirming the endo-type nature of the purified chitosanase. The optimum pH and temperature of the purified enzyme was 7.5 and 27A degrees C, respectively. Further, the enzyme was stable in the pH range of 5.5-9.0 up to 12 h and temperature between 27 and 50A degrees C up to 3 h. The enzyme was strongly inhibited by Ag+, Fe3+ and Hg2+ and stimulated by Cu+2 and Zn2+. The investigation revealed significant features regarding the stability of the chitosanase enzyme from A. fertilissima under a broad range of pH and temperature which can help in its effective use in biocontrol.
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