CN101302551A - Antierythrite production method - Google Patents

Antierythrite production method Download PDF

Info

Publication number
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
Authority
CN
China
Prior art keywords
erythritol
content
fermentation
glucose
production method
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Pending
Application number
CNA2008100168100A
Other languages
Chinese (zh)
Inventor
李悦明
张希铭
徐建春
孙慧彬
刘同照
陈金凤
曲文强
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
QINGDAO LANGYATAI (GROUP) CO Ltd
Original Assignee
QINGDAO LANGYATAI (GROUP) CO Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by QINGDAO LANGYATAI (GROUP) CO Ltd filed Critical QINGDAO LANGYATAI (GROUP) CO Ltd
Priority to CNA2008100168100A priority Critical patent/CN101302551A/en
Publication of CN101302551A publication Critical patent/CN101302551A/en
Pending legal-status Critical Current

Links

Landscapes

  • Preparation Of Compounds By Using Micro-Organisms (AREA)

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

A kind of erythritol production method
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.
CNA2008100168100A 2008-06-11 2008-06-11 Antierythrite production method Pending CN101302551A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CNA2008100168100A CN101302551A (en) 2008-06-11 2008-06-11 Antierythrite production method

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CNA2008100168100A CN101302551A (en) 2008-06-11 2008-06-11 Antierythrite production method

Publications (1)

Publication Number Publication Date
CN101302551A true CN101302551A (en) 2008-11-12

Family

ID=40112650

Family Applications (1)

Application Number Title Priority Date Filing Date
CNA2008100168100A Pending CN101302551A (en) 2008-06-11 2008-06-11 Antierythrite production method

Country Status (1)

Country Link
CN (1) CN101302551A (en)

Cited By (6)

* Cited by examiner, † Cited by third party
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

Cited By (8)

* Cited by examiner, † Cited by third party
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

Similar Documents

Publication Publication Date Title
CN101857523B (en) Method for producing xylitol and arabitol simultaneously by utilizing xylose mother liquid
CN101302551A (en) Antierythrite production method
CN109439552B (en) Aspergillus oryzae BLCY-006 and application thereof in preparation of galactooligosaccharides
CN101467780A (en) Edible fungus beverage
CN101775413B (en) Technique for producing xylitol and dulcitol simultaneously
CN107299063B (en) Preparation method of black-skin termitomyces liquid strain
CN102888332B (en) Preparation method of red date vinegar
CN101475972B (en) Method for producing L-arabinose from corncob
CN114134189B (en) Method for synchronously producing low-calorie syrup containing trehalose and erythritol
CN102994574A (en) Method for producing xylitol by employing corn stalks
CN102703525B (en) Method for increasing yield of erythritol by adjusting osmotic pressure of fermentation liquor
CN107083407B (en) Preparation, separation, impurity removal and purification method of L-malic acid
CN102703334B (en) Strain producing erythritol and method for producing erythritol by using strain
CN103911402B (en) A kind of method utilizing beet fermenting lactic acid
CN105861251B (en) A kind of blueberry mixed health wine product
CN109504733A (en) A kind of preparation method of antierythrite
JP2002017336A (en) Vinegar made from honey as raw material and method for producing the same
CN105087519B (en) Gene engineering inulinase and its method that crystal diabetin is prepared as raw material using jerusalem artichoke
CN102816802A (en) Method for producing potassium gluconate through fermentation of Aspergillus niger
CN100510089C (en) Method for preparing ethyl alcohol with watermelon
CN102796797B (en) Method for preparing xylitol and its intermediate D-xylosone by microbial transformation of glucose and strain used in the same
CN104694331A (en) Brewing method of three-berry wine
CN110172488A (en) A kind of preparation process producing isomaltoketose
CN106349311B (en) The method that S Ademetionines are extracted from yeast fermentation broth
CN107460081A (en) A kind of method that Sugarcane fruit wine is prepared using nanofiltration sugar-cane juice

Legal Events

Date Code Title Description
C06 Publication
PB01 Publication
C10 Entry into substantive examination
SE01 Entry into force of request for substantive examination
C02 Deemed withdrawal of patent application after publication (patent law 2001)
WD01 Invention patent application deemed withdrawn after publication

Application publication date: 20081112