Beer yeast cell bodies containing high ribonucleic acid content and their production method
a technology of ribonucleic acid and yeast, which is applied in the field of brewers yeast cell bodies containing can solve the problems of not being able to achieve the high ribonucleic acid conten
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example 1
[0036] The recovered brewer's yeast (which was collected after beer production) was subjected to the treatment according to this invention in a batch system in a 30-L fermentation tank. The medium for use containing nutrient ingredients consisted of the following composition, for example: 400 g ammonium sulfate, 1620 g liquid sugar, 30 g KH2PO4, 200 g NaCl, 50 g yeast extract, 16 L water and other additives such as a defoaming agent.
[0037] The yeast recovered after beer production was washed by sieving and exchanging for fresh water, and centrifuged at 3000 rpm. The obtained yeast precipitate, 4 Kg, was added to the 30-L fermentation tank containing the medium. Under aeration the activation treatment of the yeast was carried out. The treatment conditions were a pH of 4.0, a temperature of 15° C., the quantity of airflow of 1 VVM and an agitation rate of 200 rpm; and the treatment continued for 7 hours. Subsequently, the yeast cell body was recovered by centrifugation. The yeast cel...
example 2
[0038] Following the method described in Example 1, the activation treatment was carried out under the identical conditions except that only the treatment temperature of yeast was changed from 15 to 19° C. Here, the treatment time was set to be as long as 24 hours, which exceeded 7 hours in Example 1. Sampling was conducted at 0, 2, 4, 6, 8, 12, 16, 20 and 24 hours after the start of treatment and the contents of ribonucleic acid were determined. As FIG. 2 shows, the content of ribonucleic acid increased in proportion to the treatment time with the peak of the content (exceeding 10% but less than 12%) appearing 12 hours later, but showed the tendency to decrease thereafter. Therefore, the level of the increase of ribonucleic acid in weight was lowered at a treatment temperature of 10° C. relative to the 15° C. used in Example 1. The content of ribonucleic acid at the peak point reached greater than about three times that at the start of treatment. The timing for recovery under these...
example 3
[0039] The media similar to that used in Example 1 were prepared in different types, but none of them contained NaCl (sodium chloride). NaCl (200 g) was added to the media after the lapses of predetermined times from the start of treatment and the activation treatment of yeast was carried out on the respective media according to the method described in Example 1. The timing of NaCl addition was set at 2, 4, and 6 hours after the start of treatment. The contents of ribonucleic acid for the dried yeast cell bodies recovered from the respective lots were determined and plotted in FIG. 3. The content of ribonucleic acid was highest in the lot where NaCl was added 4 hours after the start of treatment and it was increased by about 40% compared to the case where NaCl was added at the time of start (Example 1). Accordingly, it has become apparent that the content of ribonucleic acid can be enhanced more by establishing the timing of NaCl addition as appropriate.
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