4.4 Article

The Possible Mechanisms Involved in Citrinin Elimination by Cryptococcus podzolicus Y3 and the Effects of Extrinsic Factors on the Degradation of Citrinin

Journal

JOURNAL OF MICROBIOLOGY AND BIOTECHNOLOGY
Volume 27, Issue 12, Pages 2119-2128

Publisher

KOREAN SOC MICROBIOLOGY & BIOTECHNOLOGY
DOI: 10.4014/jmb.1707.07051

Keywords

Citrinin; Cryptococcus podzolicus; degradation; extrinsic factor

Funding

  1. National Key Research and Development Program of China [2016YFD0400902]
  2. National Natural Science Foundation of China [31571899]
  3. Priority Academic Program Development (PAPD) of Jiangsu Higher Education Institutions

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Citrinin (CIT) is a toxic secondary metabolite produced by fungi belonging to the Penicillium, Aspergillus, and Monascus spp. This toxin has been detected in many agricultural products. In this study, a strain Y3 with the ability to eliminate CIT was screened and identified as Cryptococcus podzolicus, based on the sequence analysis of the internal transcribed spacer region. Neither uptake of CIT by cells nor adsorption by cell wall was involved in CIT elimination by Cryptococcus podzolicus Y3. The extracellular metabolites of Cryptococcus podzolicus Y3 stimulated by CIT or not showed no degradation for CIT. It indicated that CIT elimination was attributed to the degradation of intracellular enzyme(s). The degradation of CIT by C. podzolicus Y3 was dependent on the type of media, yeast concentration, temperature, pH, and initial concentration of CIT. Most of the CIT was degraded by C. podzolicus Y3 in NYDB medium at 42 h but not in PDB medium. The degradation rate of CIT was the highest (94%) when the concentration of C. podzolicus Y3 was 1 x 10(8) cells/ml. The quantity of CIT degradation was highest at 28 degrees C, and there was no degradation observed at 35 degrees C. The study also showed that acidic condition (pH 4.0) was the most favorable for CIT degradation by C. podzolicus Y3. The degradation rate of CIT increased to 98% as the concentration of CIT was increased to 20 mu g/ml. The toxicity of CIT degradation product(s) toward HEK293 was much lower than that of CIT.

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