CN101302551A - Antierythrite production method - Google Patents
Antierythrite production method Download PDFInfo
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- CN101302551A CN101302551A CNA2008100168100A CN200810016810A CN101302551A CN 101302551 A CN101302551 A CN 101302551A CN A2008100168100 A CNA2008100168100 A CN A2008100168100A CN 200810016810 A CN200810016810 A CN 200810016810A CN 101302551 A CN101302551 A CN 101302551A
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- erythritol
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- fermentation
- glucose
- production method
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Abstract
The invention discloses a method for producing erythritol. Glucose is taken as raw material, candidalipolytica is taken as a fermentation strain, shaking culture as well as first-stage and second-stage inoculum development are performed, then the fermentation in a fermentation tank is carried out, mycoprotein impurities in zymotic fluid are removed by a ceramic membrane after the fermentation is finished, then a sodium membrane is used to selectively pass through the erythritol so as to extract the erythritol, and finally the erythritol product is obtained through condensation crystallization and separation drying. The method has the advantages of short incubation period, high extraction yield, low production cost and so on.
Description
Technical field
The present invention relates to a kind of method of cultivation of erythritol.
Background technology
Erythritol is a kind of four carbon polyols that not only contained sweet taste but also empty calory.It extensively is present in marine alga, mushroom, melon, grape, pears and the leavened food; Simultaneously, also be present in the tissue and body fluid of humans and animals.Erythritol has low energy value, high dosis tolerata, has no side effect, diabetics's edible, the non-advantageous characteristic such as carious tooth that cause, and extremely is fit to be applied in the functional foodstuff.The preparation method of erythritol is mainly microbe fermentation method, and its suitability for industrialized production is to be raw material with starch, is formed through fermentation by osmophilic yeast.Present production method, fermentation period adopts Plate Filtration technology, the long control that is unfavorable for fermenting process to microbiological contamination of fermentation period more than 150 hours when fermented liquid separates, the Plate Filtration technical point is unfavorable for the removing of impurity such as tropina from fermented liquid, and extraction yield has only 75%.
Summary of the invention
Task of the present invention is to provide a kind of erythritol production method, and this method has fermentation period weak point, good separating effect, extraction yield advantages of higher.
Its technical solution is:
With glucose is raw material, and Candida lipolytica is a fermentation strain, through shaking table cultivation and one-level, secondary seed enlarged culturing, carries out ferment tank then, 25-35 ℃ of jar temperature, and tank pressure 0-0.1MPa, dissolved oxygen 20%-80% saturation ratio is at C
6H
12O
6H
2The O initial content is 20-40%, inorganic salt MgSO
47H
2O content is 0.04-0.08%, (NH
4)
2SO
4Content is 0.04-0.06%, KH
2PO
4Content is 0.10-0.15%, CuSO
4Content is 0.04-0.06%, yeast extract paste content is to ferment under the condition of 0.80-0.90%, fermentation period 100-120 hour, fermented liquid is removed tropina impurity with ceramic membrane, pass through erythritol with sodium film selectivity then, erythritol is extracted, and last condensing crystal, separation drying obtain the erythritol product.
The invention has the beneficial effects as follows: shortened fermentation period, help the control of fermenting process to microbiological contamination, guarantee the quality of fermented liquid, subsequent handlings such as the filtration ground that more helps fermented liquid carries out, and adopts membrane separation technique can improve the clarity of feed liquid, reduces because of the extraction of factor affecting products such as impurity and the quality of product, mother liquor after separating in addition can be got back to ferment tank once more, make full use of the glucose in the mother liquor, improved utilization ratio of raw materials, reduced production cost.
Embodiment
For the ease of understanding the present invention, come more detailed description the present invention below in conjunction with embodiment.Yet these embodiment just play the effect of explanation, and the present invention is not limited to these embodiment.
Embodiment 1: be raw material with glucose, Candida lipolytica is a fermentation strain, through shaking table cultivation and one-level, secondary seed enlarged culturing, carries out ferment tank at last, 25 ℃ of jar temperature, and tank pressure 0MPa, dissolved oxygen 20% saturation ratio is at C
6H
12O
6H
2The O initial content is 20%, inorganic salt MgSO
47H
2O content is 0.04%, (NH
4)
2SO
4Content is 0.04%, KH
2PO
4Content is 0.10%, CuSO
4Content is 0.04%, yeast extract paste content is to ferment under 0.80% the condition, fermentation period is 100 hours, fermented liquid is removed impurity such as tropina with ceramic membrane, pass through erythritol with U.S.'s import sodium film selectivity then, erythritol is extracted, and last condensing crystal, separation drying obtain the erythritol product.After tested, the sugar degree of erythritol is 0.07%, and extraction yield is 80%.
Embodiment 2: be raw material with glucose, Candida lipolytica is a fermentation strain, through shaking table cultivation and one-level, secondary seed enlarged culturing, carries out ferment tank at last, 30 ℃ of jar temperature, and tank pressure 0.05MPa, dissolved oxygen 50% saturation ratio is at C
6H
12O
6H
2The O initial content is 30%, inorganic salt MgSO
47H
2O content is 0.06%, (NH
4)
2SO
4Content is 0.05%, KH
2PO
4Content is 0.13%, CuSO
4Content is 0.05%, yeast extract paste content is to ferment under 0.86% the condition, fermentation period is 110 hours, fermented liquid is removed impurity such as tropina with ceramic membrane, pass through erythritol with U.S.'s import sodium film selectivity then, erythritol is extracted, and last condensing crystal, separation drying obtain the erythritol product.After tested, the sugar degree of erythritol is 0.06%, and extraction yield is 82%.
Embodiment 3: be raw material with glucose, Candida lipolytica is a fermentation strain, through shaking table cultivation and one-level, secondary seed enlarged culturing, carries out ferment tank at last, 35 ℃ of jar temperature, and tank pressure 0.1MPa, dissolved oxygen 80% saturation ratio is at C
6H
12O
6H
2The O initial content is 40%, inorganic salt MgSO
47H
2O content is 0.08%, (NH
4)
2SO
4Content is 0.06%, KH
2PO
4Content is 0.15%, CuSO
4Content is 0.06%, yeast extract paste content is to ferment under 0.90% the condition, fermentation period is 120 hours, fermented liquid is removed impurity such as tropina with ceramic membrane, pass through erythritol with U.S.'s import sodium film selectivity then, erythritol is extracted, and last condensing crystal, separation drying obtain the erythritol product.After tested, the sugar degree of erythritol is 0.08%, and extraction yield is 81%.
Claims (1)
1, a kind of erythritol production method, it is characterized in that: be raw material with glucose, Candida lipolytica is a fermentation strain, through shaking table cultivation and one-level, secondary seed enlarged culturing, carry out ferment tank then, at 25-35 ℃ of jar temperature, tank pressure 0-0.1MPa, dissolved oxygen 20%-80% saturation ratio is at C
6H
12O
6H
2The O initial content is 20-40%, inorganic salt MgSO
47H
2O content is 0.04-0.08%, (NH
4)
2SO
4Content is 0.04-0.06%, KH
2PO
4Content is 0.10-0.15%, CuSO
4Content is 0.04-0.06%, yeast extract paste content is to ferment under the condition of 0.80-0.90%, fermentation period 100-120 hour, fermented liquid is removed tropina impurity with ceramic membrane, pass through erythritol with sodium film selectivity then, erythritol is extracted, and last condensing crystal, separation drying obtain the erythritol product.
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CNA2008100168100A CN101302551A (en) | 2008-06-11 | 2008-06-11 | Antierythrite production method |
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CNA2008100168100A CN101302551A (en) | 2008-06-11 | 2008-06-11 | Antierythrite production method |
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CN101302551A true CN101302551A (en) | 2008-11-12 |
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Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN102154383A (en) * | 2010-12-29 | 2011-08-17 | 保龄宝生物股份有限公司 | Method for producing phycite by using corn meal |
CN102703525A (en) * | 2012-06-20 | 2012-10-03 | 江南大学 | Method for increasing yield of erythritol by adjusting osmotic pressure of fermentation liquor |
CN104694585A (en) * | 2015-04-02 | 2015-06-10 | 诸城东晓生物科技有限公司 | Production method of erythritol |
CN104726503A (en) * | 2015-04-03 | 2015-06-24 | 诸城东晓生物科技有限公司 | Method for producing erythritol in fermentation tank |
CN105624227A (en) * | 2016-03-01 | 2016-06-01 | 苏州艾缇克药物化学有限公司 | Method for preparing (S)-3-hydroxytetrahydrofuran based on erythritol microorganisms |
CN110564782A (en) * | 2019-09-23 | 2019-12-13 | 安徽丰原生物化学股份有限公司 | Erythritol fermentation production method |
-
2008
- 2008-06-11 CN CNA2008100168100A patent/CN101302551A/en active Pending
Cited By (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN102154383A (en) * | 2010-12-29 | 2011-08-17 | 保龄宝生物股份有限公司 | Method for producing phycite by using corn meal |
CN102154383B (en) * | 2010-12-29 | 2011-11-30 | 保龄宝生物股份有限公司 | Method for producing phycite by using corn meal |
CN102703525A (en) * | 2012-06-20 | 2012-10-03 | 江南大学 | Method for increasing yield of erythritol by adjusting osmotic pressure of fermentation liquor |
CN102703525B (en) * | 2012-06-20 | 2013-10-30 | 江南大学 | Method for increasing yield of erythritol by adjusting osmotic pressure of fermentation liquor |
CN104694585A (en) * | 2015-04-02 | 2015-06-10 | 诸城东晓生物科技有限公司 | Production method of erythritol |
CN104726503A (en) * | 2015-04-03 | 2015-06-24 | 诸城东晓生物科技有限公司 | Method for producing erythritol in fermentation tank |
CN105624227A (en) * | 2016-03-01 | 2016-06-01 | 苏州艾缇克药物化学有限公司 | Method for preparing (S)-3-hydroxytetrahydrofuran based on erythritol microorganisms |
CN110564782A (en) * | 2019-09-23 | 2019-12-13 | 安徽丰原生物化学股份有限公司 | Erythritol fermentation production method |
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Application publication date: 20081112 |