Standardisation of assay procedure and some properties of ribonuclease from Aspergillus candidus.
IR@CSIR-CFTRI
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Relation |
http://ir.cftri.com/5477/
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Title |
Standardisation of assay procedure and some properties of ribonuclease from Aspergillus candidus.
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Creator |
Mohammad Kunhi, A. A.
Singh, R. |
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Subject |
03 Fungi
05 Enzymes |
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Description |
Screening of several fungal cultures resulted in the selection of an isolate of Aspergillus candidus which produced a considerable amount of RNA-degrading enzyme in both surface and submerged methods of cultivation. The conditions for the assay of the RNAase were standardized at pH 4.5, 55 ~ and using 0.25 ~o yeast RNA as substrate. The enzyme was stable at pit 5.2. EDTA was found to activate the enzyme slightly. At temperatures 50-- 60 ~ there was considerable loss in enzyme activity which was traced to the presence of a contaminating protease which presumably degraded the RNAase optimally at this temperature. The protease could be preferentially inactivated at or above 75 ~ The crude enzyme, in addition to RNAaso was found to possess DNAase, nonspecific phosphodiesterase and 3'- and 5'-phosphomonoesterase activities. |
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Date |
1981
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Type |
Article
PeerReviewed |
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Format |
pdf
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Language |
en
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Identifier |
http://ir.cftri.com/5477/1/Folia%20Microbiol.%2026%2C%20328--333%20%281981%29.pdf
Mohammad Kunhi, A. A. and Singh, R. (1981) Standardisation of assay procedure and some properties of ribonuclease from Aspergillus candidus. Folia Microbiologica, 26 (4). pp. 328-333. |
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