US2015104557A1PendingUtilityA1

Method for the cultivation of microorganisms of the genus thraustochytriales by using an optimized low salt medium

Assignee: NUTRINOVA GMBHPriority: Nov 10, 2003Filed: Oct 28, 2014Published: Apr 16, 2015
Est. expiryNov 10, 2023(expired)· nominal 20-yr term from priority
A23K 1/146A23L 1/3008A23V 2002/00C12P 7/6427A23L 33/12C12N 1/12A23K 10/37C12N 1/14C12P 7/64C12P 7/6434C12P 7/6472
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Claims

Abstract

The invention relates to an optimized method for cultivating microorganisms of the genus Thraustochytriales , according to which the microorganisms are cultivated in a low salt medium without adding sodium salts and chloride salts, the total salt content being less than 3.5 g/L (corresponding to less than 10 percent of sea water salt content), whereupon the PUFAs are isolated from the microorganisms and/or the medium. The invention especially relates to novel optimized media having a substantially reduced total salt content, above all a particularly reduced NaCl content. The production of PUFAs can be substantially improved and significantly simplified by using a novel combination of different salts as a media composition in which the overall weight ratios of ions do not exceed 1.75 g/L. Furthermore, said medium preferably contains no added sodium salt and chloride salt at all, which helps prevent environmental damages caused by wastewaters containing salt.

Claims

exact text as granted — not AI-modified
1 . A method for cultivating microorganisms of the order  Thraustochytriales , wherein the microorganisms are cultivated in a fermentation medium without adding sodium salts and chloride salts, the total salt content is less than 3.5 g/L of total salts. 
     
     
         2 . The method according to  claim 1 , wherein the microorganisms bring forth a production of more than 30 wt % oil per unit of weight of dry biomass. 
     
     
         3 . The method according to  claim 1 , wherein up to 3 g/L CaCO 3 . 
     
     
         4 . The method according to  claim 1 , wherein the microorganisms bring forth a production of more than 10% DHA per dry biomass. 
     
     
         5 . The method according to  claim 1 , wherein the microorganisms bring forth a production of more than 5% DPA per dry biomass. 
     
     
         6 . The method according to  claim 1 , characterized by the use of the fermentation medium, the total salt content of which is in the range <15% of the salt content of sea water. 
     
     
         7 . The method according to  claim 1 , characterized in that the sum of the weight fractions of Na +  and Cl −  ions in the low salt medium comprises less than 1.75 g/L. 
     
     
         8 . The method according to  claim 1 , characterized in that the total sodium content of the fermentation medium is less than 150 mg/L. 
     
     
         9 . The method according to  claim 1 , characterized in that the total chloride content of the fermentation medium is less than 250 mg/L. 
     
     
         10 . The method according to  claim 1 , characterized in that the fermentation medium comprises glucose, yeast extract, magnesium sulfate, calcium carbonate and potassium phosphate. 
     
     
         11 . The method according to  claim 1 , characterized in that the fermentation medium comprises glucose, corn steep liquor, magnesium sulfate, calcium carbonate and potassium phosphate. 
     
     
         12 . The method according to  claim 10 , characterized in that the fermentation medium comprises magnesium sulfate, calcium carbonate and potassium phosphate at less than 3 g/L each. 
     
     
         13 . The method according to  claim 1 , characterized in that the fermentation medium has a pH value of between 3 and 10. 
     
     
         14 . The method according to  claim 1 , characterized in that the cultivation takes place between 10° C. and 40° C. 
     
     
         15 . The method according to  claim 1 , characterized in that the cultivation takes place for 1 to 10 days. 
     
     
         16 . The method according to  claim 1 , characterized in that the microorganism belongs to the genus  Schizochytrium, Thraustochytrium  or  Ulkenia.    
     
     
         17 . The method according to  claim 1 , characterized in that the microorganism is  Ulkenia  sp. SAM 2179. 
     
     
         18 . The method according to  claim 1 , characterized in that the microorganism is  Schizochytrium  sp. SR 21. 
     
     
         19 . Oil having a content of at least 10% DHA, produced using a method according to  claim 1  and subsequent isolation of the oil from the culture broth and/or the biomass available therein. 
     
     
         20 . Oil having a content of at least 5% DHA, produced using a method according to  claim 1  and subsequent isolation of the oil from the culture broth and/or the biomass available therein. 
     
     
         21 . DHA of at least 90% purity, produced using a method according to  claim 1  and subsequent isolation of the DHA from the culture broth and/or the biomass available therein. 
     
     
         22 . DPA of at least 90% purity, produced using a method according to  claim 1  and subsequent isolation of the DPA from the culture broth and/or the biomass available therein. 
     
     
         23 . Biomass obtainable by means of a method according to  claim 1  and subsequent separation of the biomass from the culture broth. 
     
     
         24 . Animal feed comprising biomass according to  claim 23 . 
     
     
         25 . Foodstuff for human nutrition comprising biomass according to  claim 23 .

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