Purification and characterization of a novel cold‐adapted phytase from Rhodotorula mucilaginosa strain JMUY14 isolated from Antarctic
A yeast producing a cold‐adapted phytase was isolated from Antarctic deep‐sea sediment and identified as a Rhodotorula mucilaginosa strain JMUY14 of basidiomycetous yeasts. It was cultured in fermentation optimized by a response surface methodology based on the Box–Behnken design. The maximum activi...
Published in: | Journal of Basic Microbiology |
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Main Authors: | , , |
Other Authors: | |
Format: | Article in Journal/Newspaper |
Language: | English |
Published: |
Wiley
2015
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Subjects: | |
Online Access: | http://dx.doi.org/10.1002/jobm.201400865 https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1002%2Fjobm.201400865 https://onlinelibrary.wiley.com/doi/pdf/10.1002/jobm.201400865 |
Summary: | A yeast producing a cold‐adapted phytase was isolated from Antarctic deep‐sea sediment and identified as a Rhodotorula mucilaginosa strain JMUY14 of basidiomycetous yeasts. It was cultured in fermentation optimized by a response surface methodology based on the Box–Behnken design. The maximum activity of phytase reached 205.447 U ml −1 , which was close to the predicted value of 201.948 U ml −1 and approximately 3.4 times higher than its initial activity. The extracellular phytase was purified by 15.2‐fold to homogeneity with a specific activity of 31,635 U mg −1 by (NH 4 ) 2 SO 4 precipitation, and a combination of DEAE Sepharose Fast Flow, SP Sepharose Fast Flow, and Sephadex G‐100. The molecular weight of the purified enzyme was estimated to be 63 kDa and its pI was 4.33. Its optimal temperature and pH were 50 °C and 5.0, respectively. Its activity was 85% at 37 °C, and showed good stability at pH 3.0∼7.0. When compared with mesophilic counterparts, the phytase not only exhibited a higher activity during 20∼30 °C but also had a low K m (247 µM) and high k cat (1394 s −1 ). The phytase activity was slightly stimulated in the presence of Mg 2+ , Fe 2+ , Fe 3+ , K + , Na + , Ca 2+ , EDTA, and EGTA and moderately inhibited by Cu 2+ , Zn 2+ , Mn 2+ , Ag + , PMSF, SDS, and phenylgloxal hydrate. It was resistant to both pepsin and trypsin. Since the phytase produced by the R. mucilaginosa JMUY14 showed a high specific activity, good pH stability, strong protease resistance, and high activity at low temperature, it has great potential for feed applications, especially in aquaculture. |
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