CN102603814B - Method for increasing crystalizing efficiency of xylose in xylose mother solution - Google Patents
Method for increasing crystalizing efficiency of xylose in xylose mother solution Download PDFInfo
- Publication number
- CN102603814B CN102603814B CN201210056432.5A CN201210056432A CN102603814B CN 102603814 B CN102603814 B CN 102603814B CN 201210056432 A CN201210056432 A CN 201210056432A CN 102603814 B CN102603814 B CN 102603814B
- Authority
- CN
- China
- Prior art keywords
- xylose
- efficiency
- xylose mother
- liquid
- filtration
- 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.)
- Expired - Fee Related
Links
- SRBFZHDQGSBBOR-IOVATXLUSA-N D-xylopyranose Chemical compound O[C@@H]1COC(O)[C@H](O)[C@H]1O SRBFZHDQGSBBOR-IOVATXLUSA-N 0.000 title claims abstract description 109
- PYMYPHUHKUWMLA-UHFFFAOYSA-N arabinose Natural products OCC(O)C(O)C(O)C=O PYMYPHUHKUWMLA-UHFFFAOYSA-N 0.000 title claims abstract description 61
- SRBFZHDQGSBBOR-UHFFFAOYSA-N beta-D-Pyranose-Lyxose Natural products OC1COC(O)C(O)C1O SRBFZHDQGSBBOR-UHFFFAOYSA-N 0.000 title claims abstract description 61
- 238000000034 method Methods 0.000 title claims abstract description 20
- 239000010413 mother solution Substances 0.000 title abstract 4
- 238000000855 fermentation Methods 0.000 claims abstract description 38
- 230000004151 fermentation Effects 0.000 claims abstract description 38
- 240000004808 Saccharomyces cerevisiae Species 0.000 claims abstract description 23
- 238000001914 filtration Methods 0.000 claims abstract description 22
- 230000001954 sterilising effect Effects 0.000 claims abstract 2
- 239000007788 liquid Substances 0.000 claims description 35
- 239000012528 membrane Substances 0.000 claims description 28
- 235000014680 Saccharomyces cerevisiae Nutrition 0.000 claims description 21
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 8
- 238000005374 membrane filtration Methods 0.000 claims description 8
- 238000000108 ultra-filtration Methods 0.000 claims description 8
- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonia chloride Chemical compound [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 claims description 6
- 239000003085 diluting agent Substances 0.000 claims description 5
- 239000011148 porous material Substances 0.000 claims description 5
- 229910052757 nitrogen Inorganic materials 0.000 claims description 4
- 235000016709 nutrition Nutrition 0.000 claims description 4
- 230000035764 nutrition Effects 0.000 claims description 4
- 239000002994 raw material Substances 0.000 claims description 4
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 claims description 3
- 235000019270 ammonium chloride Nutrition 0.000 claims description 3
- BFNBIHQBYMNNAN-UHFFFAOYSA-N ammonium sulfate Chemical compound N.N.OS(O)(=O)=O BFNBIHQBYMNNAN-UHFFFAOYSA-N 0.000 claims description 3
- 229910052921 ammonium sulfate Inorganic materials 0.000 claims description 3
- 235000011130 ammonium sulphate Nutrition 0.000 claims description 3
- 239000004202 carbamide Substances 0.000 claims description 3
- 235000013877 carbamide Nutrition 0.000 claims description 3
- 238000003756 stirring Methods 0.000 claims description 3
- 241000235347 Schizosaccharomyces pombe Species 0.000 claims description 2
- 230000004907 flux Effects 0.000 claims description 2
- 239000002054 inoculum Substances 0.000 claims description 2
- 230000001105 regulatory effect Effects 0.000 claims 1
- 229930182830 galactose Natural products 0.000 abstract description 15
- WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 abstract description 9
- 239000000084 colloidal system Substances 0.000 abstract description 9
- 239000008103 glucose Substances 0.000 abstract description 9
- PYMYPHUHKUWMLA-WDCZJNDASA-N arabinose Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)C=O PYMYPHUHKUWMLA-WDCZJNDASA-N 0.000 abstract description 6
- 239000000243 solution Substances 0.000 abstract description 6
- 239000000126 substance Substances 0.000 abstract description 5
- 102000004169 proteins and genes Human genes 0.000 abstract description 4
- 108090000623 proteins and genes Proteins 0.000 abstract description 4
- WQZGKKKJIJFFOK-PHYPRBDBSA-N alpha-D-galactose Chemical compound OC[C@H]1O[C@H](O)[C@H](O)[C@@H](O)[C@H]1O WQZGKKKJIJFFOK-PHYPRBDBSA-N 0.000 abstract description 3
- 230000000694 effects Effects 0.000 abstract description 3
- WQZGKKKJIJFFOK-VFUOTHLCSA-N beta-D-glucose Chemical compound OC[C@H]1O[C@@H](O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-VFUOTHLCSA-N 0.000 abstract description 2
- 238000004519 manufacturing process Methods 0.000 abstract description 2
- 239000012530 fluid Substances 0.000 abstract 3
- 238000007865 diluting Methods 0.000 abstract 1
- 235000012041 food component Nutrition 0.000 abstract 1
- 230000002503 metabolic effect Effects 0.000 abstract 1
- 239000012452 mother liquor Substances 0.000 description 18
- 239000000706 filtrate Substances 0.000 description 7
- 239000006228 supernatant Substances 0.000 description 7
- 238000002425 crystallisation Methods 0.000 description 5
- 230000008025 crystallization Effects 0.000 description 5
- 239000012535 impurity Substances 0.000 description 5
- 238000005119 centrifugation Methods 0.000 description 4
- 229920002521 macromolecule Polymers 0.000 description 4
- 239000002207 metabolite Substances 0.000 description 4
- 238000000926 separation method Methods 0.000 description 4
- 241000894006 Bacteria Species 0.000 description 3
- 239000004744 fabric Substances 0.000 description 3
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 2
- 239000012141 concentrate Substances 0.000 description 2
- 238000010790 dilution Methods 0.000 description 2
- 239000012895 dilution Substances 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- 238000000746 purification Methods 0.000 description 2
- 238000009423 ventilation Methods 0.000 description 2
- 241000609240 Ambelania acida Species 0.000 description 1
- 239000005909 Kieselgur Substances 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- 240000008042 Zea mays Species 0.000 description 1
- 235000005824 Zea mays ssp. parviglumis Nutrition 0.000 description 1
- 235000002017 Zea mays subsp mays Nutrition 0.000 description 1
- 239000010905 bagasse Substances 0.000 description 1
- 230000000903 blocking effect Effects 0.000 description 1
- 239000006227 byproduct Substances 0.000 description 1
- 235000005822 corn Nutrition 0.000 description 1
- 238000009295 crossflow filtration Methods 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 238000004042 decolorization Methods 0.000 description 1
- 230000007812 deficiency Effects 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 235000013305 food Nutrition 0.000 description 1
- 238000004128 high performance liquid chromatography Methods 0.000 description 1
- 230000007062 hydrolysis Effects 0.000 description 1
- 238000006460 hydrolysis reaction Methods 0.000 description 1
- 229910052943 magnesium sulfate Inorganic materials 0.000 description 1
- 235000019341 magnesium sulphate Nutrition 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 229910000402 monopotassium phosphate Inorganic materials 0.000 description 1
- 235000019796 monopotassium phosphate Nutrition 0.000 description 1
- 235000015097 nutrients Nutrition 0.000 description 1
- PJNZPQUBCPKICU-UHFFFAOYSA-N phosphoric acid;potassium Chemical compound [K].OP(O)(O)=O PJNZPQUBCPKICU-UHFFFAOYSA-N 0.000 description 1
- 238000009991 scouring Methods 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- -1 xylose Small molecules Chemical class 0.000 description 1
Landscapes
- Preparation Of Compounds By Using Micro-Organisms (AREA)
- Separation Using Semi-Permeable Membranes (AREA)
Abstract
Description
(一) 技术领域 (1) Technical field
本发明属于生物和化工领域,特别涉及一种提高木糖母液中木糖结晶效率的方法。 The present invention belongs to the fields of biology and chemical industry, and in particular relates to a method for improving the crystallization efficiency of xylose in xylose mother liquor.
(二) 背景技术 (2) Background technology
木糖产品主要是以玉米芯、甘蔗渣等为原料,经水解、净化、蒸发、结晶、离心、烘干等工序制成的白色结晶体,在轻工、食品、化工行业中具有广泛的用途。木糖母液浓度在60%左右,其中木糖40~50%,另外,葡萄糖15~20%,阿拉伯糖15~30%,半乳糖8~12%,由于这些组分的存在,木糖母液无法结晶,只能作为副产品出售。 Xylose products are mainly white crystals made from corn cobs and bagasse through hydrolysis, purification, evaporation, crystallization, centrifugation, drying and other processes. They are widely used in light industry, food and chemical industries. The concentration of xylose mother liquor is about 60%, of which xylose is 40~50%, in addition, glucose is 15~20%, arabinose is 15~30%, galactose is 8~12%, due to the existence of these components, xylose mother liquor cannot Crystallized and sold only as a by-product.
虽然目前有报道利用模拟移动床提纯木糖母液生产木糖和阿拉伯糖的工艺(专利号200710014175.8),并且已规模化生产,但木糖母液的预处理不彻底,其中存在的半乳糖、胶体、蛋白以及酵母发酵产生的代谢产物以及破碎的菌体不能彻底除去,给脱色过滤带来了很大的难度。由于传统的真空转鼓过滤和板框过滤工艺,液体流动的方向和过滤的方向是一致的,液体中胶体等杂质很快直接附着在过滤介质上,将过滤介质堵塞,不能除去料液中所含的胶体和蛋白等物质,一般板框过滤脱色后的发酵液,平均每平方米滤布的过滤量在2~3m3,之后不得不更换滤布,进行清洗;另外,真空转鼓过滤过程中还需消耗大量的硅藻土等助滤剂,一方面增加了过滤的运行成本,另一方面助滤剂可以带走部分物料,增加了物料的损失;最后,由于木糖和半乳糖的HPLC色谱峰距离很近,利用模拟移动床分离液不能将半乳糖从木糖组分中出去,导致半乳糖大部分都存在于木糖组分中,使木糖的纯度大幅度降低,半乳糖的存在使得木糖结晶的收率在30%左右。 Although it has been reported to use a simulated moving bed to purify the xylose mother liquor to produce xylose and arabinose (patent number 200710014175.8), and it has been produced on a large scale, the pretreatment of the xylose mother liquor is not thorough, and the galactose, colloid, Proteins, metabolites produced by yeast fermentation and broken bacteria cannot be completely removed, which brings great difficulty to decolorization and filtration. Due to the traditional vacuum drum filtration and plate-and-frame filtration process, the direction of liquid flow is consistent with the direction of filtration. Impurities such as colloids in the liquid will directly adhere to the filter medium quickly, blocking the filter medium and unable to remove all impurities in the liquid. Colloid and protein and other substances contained in the plate and frame filter decolorized fermentation broth, the average filtration capacity of filter cloth per square meter is 2~3m 3 , and then the filter cloth has to be replaced and cleaned; in addition, the vacuum drum filtration process It also needs to consume a large amount of filter aids such as diatomaceous earth, which increases the operating cost of filtration on the one hand, and on the other hand, filter aids can take away part of the material, increasing the loss of materials; finally, due to the xylose and galactose The distance between the HPLC chromatographic peaks is very close, and the galactose cannot be removed from the xylose component by using the simulated moving bed separation liquid, resulting in most of the galactose existing in the xylose component, which greatly reduces the purity of xylose, and the galactose The presence of xylose makes the yield of xylose crystallization about 30%.
(三) 发明内容 (3) Contents of the invention
本发明为了弥补现有技术的不足,提供了一种步骤简单、分离精度高的提高木糖母液中木糖结晶效率的方法。 In order to make up for the deficiencies of the prior art, the present invention provides a method for improving the crystallization efficiency of xylose in xylose mother liquor with simple steps and high separation precision.
本发明是通过如下技术方案实现的: The present invention is achieved through the following technical solutions:
一种提高木糖母液中木糖结晶效率的方法,以木糖母液为原料,主要包括如下步骤: A method for improving xylose crystallization efficiency in xylose mother liquor, using xylose mother liquor as raw material, mainly includes the following steps:
(1)将木糖母液稀释至15~25%的浓度后加入占稀释液重量0.1~1%的氮素营养,然后调节稀释液的pH值为4.0~4.5,于115~120℃下灭菌30分钟,降温至24~26℃后接入酵母菌种,接种量为每升稀释液12g干酵母,然后于20~40℃下进行发酵; (1) Dilute the xylose mother liquor to a concentration of 15~25%, add nitrogen nutrition accounting for 0.1~1% of the weight of the diluted solution, then adjust the pH value of the diluted solution to 4.0~4.5, and sterilize at 115~120°C After 30 minutes, cool down to 24~26°C and insert yeast strains, the inoculum amount is 12g of dry yeast per liter of dilution, and then ferment at 20~40°C;
(2)将发酵液离心,离心清液打回发酵罐,浓液打入酵母罐储存; (2) Centrifuge the fermentation broth, return the centrifuged supernatant to the fermenter, and pour the concentrated liquid into the yeast tank for storage;
(3)将离心清液经错流管式膜于35~80℃下过滤,采用膜孔径为1000Da~0.1微米的超滤膜,超滤清液收集入超滤液罐,超滤浓液再次经过离心,回收料液。 (3) Filtrate the centrifuged supernatant through a cross-flow tubular membrane at 35-80°C, using an ultrafiltration membrane with a membrane pore size of 1000Da~0.1 micron, collect the ultrafiltrate into the ultrafiltrate tank, and ultrafiltrate the concentrate again After centrifugation, the feed liquid is recovered.
本发明将木糖母液稀释后,加入营养成分,灭菌,然后接种酵母进行发酵,出去木糖母液中的葡萄糖和半乳糖,发酵液离心分离出酵母后,发酵清液通过错流管膜过滤处理,除去发酵液中所含的胶体以及发酵过程中产生的游离蛋白等发酵代谢产物,最后得到含木糖和阿拉伯糖的超滤清液,用于后续生产。 The invention dilutes the xylose mother liquor, adds nutrients, sterilizes, inoculates yeast for fermentation, removes glucose and galactose in the xylose mother liquor, centrifuges the fermentation liquor to separate the yeast, and filters the fermentation supernatant through a cross-flow tube membrane Treatment, removal of fermentation metabolites such as colloids contained in the fermentation broth and free protein produced during the fermentation process, and finally an ultrafiltrate containing xylose and arabinose is obtained for subsequent production.
本发明的更优方案为: A better solution of the present invention is:
步骤(1)中,氮素营养为尿素、氯化铵或硫酸铵,其加入量为稀释液重量的0.3~0.5%。 In step (1), the nitrogen nutrition is urea, ammonium chloride or ammonium sulfate, and the amount added is 0.3-0.5% of the weight of the diluent.
步骤(1)中,酵母菌种为面包酵母、啤酒酵母或粟酒裂殖酵母中的一种或多种。 In step (1), the yeast strain is one or more of baker's yeast, brewer's yeast or Schizosaccharomyces pombe.
步骤(1)中,发酵时,通气量为1:0.1~0.4,搅拌速度为50~100转/min,发酵时间为48h。 In step (1), during fermentation, the ventilation rate is 1:0.1-0.4, the stirring speed is 50-100 rpm, and the fermentation time is 48 hours.
步骤(2)中,发酵液离心采用碟片式离心机。 In step (2), a disc centrifuge is used for the centrifugation of the fermentation broth.
步骤(3)中,超滤膜孔径为100000Da,运行温度为35~40℃,过滤压力位0.05~0.3MPa,平均通量为60L/m2·h。 In step (3), the pore size of the ultrafiltration membrane is 100,000 Da, the operating temperature is 35~40°C, the filtration pressure is 0.05~0.3MPa, and the average flux is 60L/m 2 ·h.
步骤(3)中,所述错流管式膜过滤包括循环过滤和连续过滤,连续过滤时,离心清液进入膜过滤设备,经过一次膜过滤后,膜前液继续进入第二组超滤膜,最后至第三组超滤膜,超滤液统一收集于超滤液罐,膜前液收集于离心前罐,混合下一批料液后再次经过离心、超滤,达到最大化利用料液的目的;循环过滤时,离心清液进入膜过滤设备,经过一定的循环时间,超滤清液收集于超滤液罐,而超滤浓液再次经过离心,回收料液。 In step (3), the cross-flow tubular membrane filtration includes circulation filtration and continuous filtration. During continuous filtration, the centrifuged liquid enters the membrane filtration equipment, and after a membrane filtration, the pre-membrane liquid continues to enter the second set of ultrafiltration membranes , and finally to the third group of ultrafiltration membranes, the ultrafiltrate is collected in the ultrafiltrate tank uniformly, the pre-membrane liquid is collected in the centrifuge front tank, and the next batch of feed liquid is mixed and then centrifuged and ultrafiltered again to maximize the use of feed liquid The purpose; during circulation filtration, the centrifuged supernatant enters the membrane filtration equipment, after a certain cycle time, the ultrafiltrated supernatant is collected in the ultrafiltrate tank, and the ultrafiltered concentrate is centrifuged again to recover the feed liquid.
本发明基于酵母发酵、模拟移动床提纯木糖母液的基础上,寻求一种能彻底除去木糖母液中半乳糖、胶体以及酵母发酵过程中产生的破碎菌体和代谢产物的方法,得到比较纯净的木糖和阿拉伯糖的混合液。 On the basis of yeast fermentation and simulated moving bed purification of xylose mother liquor, the present invention seeks a method that can completely remove galactose, colloid, and broken bacteria and metabolites produced in the xylose mother liquor in the yeast fermentation process, and obtain relatively pure A mixture of xylose and arabinose.
本发明利用错流管式膜过滤工艺,使发酵液在一定压力下通过错流管式膜,收集滤过液作为下工序原料。错流管式过滤工艺,液体流动方向和过滤方向呈垂直状态,过滤方向垂直于膜表面,液体流动方向则平行于膜表面;由于液体的快速流动,使得胶体等杂质不能停留在过滤介质表面,即使杂质暂时附着在过滤介质表面,快速流动的液体可以及时将其冲刷掉,所以错流式过滤不容易堵塞过滤介质,由于木糖母液中所含的杂质存在分子量上的巨大差别,胶体以及酵母发酵过程中产生的破碎菌体和代谢产物属于大分子物质,分子量在十万或几十万以上,而木糖、阿拉伯糖等微小分子物质,分子量在几百左右,所以利用膜设备可以将胶体等大分子物质截留,而木糖等成分则可以透过膜,在滤过液一端聚集,由于本发明采用错流管式膜过滤,发酵液在膜一侧以切线方向高速通过,而木糖等小分子以垂直于膜的方向通过,大分子被截留在膜的发酵液一侧,由于发酵液高速流动的冲刷作用,使大分子物质不能在膜表面停留,不容易堵塞膜孔,发酵液经过膜过滤工艺以后,活性炭脱色后板框过滤时平均每平方米滤布的过滤量可达到8~10m3. The invention utilizes the cross-flow tubular membrane filtration process to make the fermented liquid pass through the cross-flow tubular membrane under a certain pressure, and collect the filtrate as the raw material for the next process. In the cross-flow tubular filtration process, the liquid flow direction and the filtration direction are perpendicular, the filtration direction is perpendicular to the membrane surface, and the liquid flow direction is parallel to the membrane surface; due to the rapid flow of the liquid, impurities such as colloids cannot stay on the surface of the filter medium. Even if the impurities are temporarily attached to the surface of the filter medium, the fast-flowing liquid can wash them away in time, so cross-flow filtration is not easy to block the filter medium. Due to the huge difference in molecular weight of the impurities contained in the xylose mother liquor, colloids and yeast The broken bacteria and metabolites produced during the fermentation process belong to macromolecular substances with a molecular weight of more than 100,000 or hundreds of thousands, while micromolecular substances such as xylose and arabinose have a molecular weight of about several hundred, so the colloid can be separated by using membrane equipment. Macromolecular substances such as xylose are intercepted, while xylose and other components can pass through the membrane and gather at one end of the filtrate. Since the present invention adopts cross-flow tubular membrane filtration, the fermentation broth passes through the membrane side at a high speed in a tangential direction, while the xylose Small molecules pass through in a direction perpendicular to the membrane, and macromolecules are trapped on the side of the fermentation broth of the membrane. Due to the scouring effect of the high-speed flow of the fermentation broth, the macromolecules cannot stay on the surface of the membrane, and it is not easy to block the pores of the membrane. After the membrane filtration process, the average filtration capacity per square meter of filter cloth can reach 8~10m 3 .
本发明步骤简单,处理成本低,分离精度高,分离效果好,大大减轻了后续处理难度,可大幅度提高产品收率,适于广泛推广应用。 The invention has simple steps, low processing cost, high separation precision and good separation effect, greatly reduces the difficulty of follow-up processing, can greatly increase product yield, and is suitable for wide popularization and application.
(四) 具体实施方式 (4) Specific implementation methods
实施例1: Example 1:
取稀释至20%木糖母液200ml,调pH4.3,加入1g尿素,灭菌后冷却至室温。接种面包酵母2.4g添加面包酵母,于35℃摇床中,进行发酵。发酵24小时后,发酵液浓度为17.4%,测定葡萄糖的含量为0.23%,半乳糖含量12.32%,48小时后,葡萄糖含量为0,半乳糖含量为1.72%。 Take 200ml of xylose mother liquor diluted to 20%, adjust pH to 4.3, add 1g of urea, sterilize and cool to room temperature. Inoculate 2.4 g of baker's yeast, add baker's yeast, and ferment in a shaker at 35°C. After 24 hours of fermentation, the concentration of the fermented liquid was 17.4%, the measured glucose content was 0.23%, and the galactose content was 12.32%. After 48 hours, the glucose content was 0, and the galactose content was 1.72%.
实施例2: Example 2:
取稀释至20%木糖母液200ml,调pH4.7,加入1g氯化铵,灭菌后冷却至室温。接种面包酵母2.4g添加面包酵母,于35℃摇床中,进行发酵。发酵24小时后,发酵液浓度为17.8%,测定葡萄糖的含量为0,半乳糖含量6.828%,48小时后,葡萄糖含量为0,半乳糖含量为1.587%。 Take 200ml of xylose mother liquor diluted to 20%, adjust the pH to 4.7, add 1g of ammonium chloride, sterilize and cool to room temperature. Inoculate 2.4 g of baker's yeast, add baker's yeast, and ferment in a shaker at 35°C. After 24 hours of fermentation, the concentration of the fermentation broth was 17.8%, the measured glucose content was 0, and the galactose content was 6.828%. After 48 hours, the glucose content was 0, and the galactose content was 1.587%.
实施例3: Example 3:
将木糖母液原料用泵打入30m3发酵罐中,加入工艺用水稀释至浓度为21.5%,稀释液约占发酵罐容积的2/3。按0.4%比例加入磷酸二氢钾、硫酸铵和硫酸镁,调节pH4.4,于115~120℃灭菌30min,待温度降至35℃后, 接种360kg面包酵母,开始发酵。发酵条件为:温度35~38℃,pH4.0~4.5,搅拌速度64转/min,通风量1:0.2。发酵约9h后浓度为18.2%,测定发酵液中葡萄糖的含量为0.37%,半乳糖含量为12.54%。发酵48小时后,葡萄糖含量为0,半乳糖含量为1.39%,结束发酵。然后将发酵液打入碟片离心机进行离心。发酵液经碟片离心机离心后,清液打回发酵罐,浓液打入酵母罐储存。 Pump the xylose mother liquor raw material into a 30m3 fermentation tank, add process water to dilute to a concentration of 21.5%, and the dilution accounts for about 2/3 of the volume of the fermentation tank. Add potassium dihydrogen phosphate, ammonium sulfate and magnesium sulfate at a ratio of 0.4%, adjust the pH to 4.4, and sterilize at 115-120°C for 30 minutes. After the temperature drops to 35°C, inoculate 360kg of baker's yeast and start fermentation. The fermentation conditions are: temperature 35~38°C, pH 4.0~4.5, stirring speed 64 rpm, ventilation rate 1:0.2. After about 9 hours of fermentation, the concentration was 18.2%, the glucose content in the fermentation broth was determined to be 0.37%, and the galactose content was 12.54%. After 48 hours of fermentation, the glucose content was 0, the galactose content was 1.39%, and the fermentation ended. The fermentation broth is then put into a disc centrifuge for centrifugation. After the fermentation liquid is centrifuged by a disc centrifuge, the clear liquid is returned to the fermenter, and the thick liquid is transferred to the yeast tank for storage.
实施例4: Example 4:
木糖母液发酵液502kg,浓度为17.8%,温度为34℃,过滤压力0.1~0.3MPa。所用膜孔径为100,000Da,通过膜设备后,得到滤液466.144kg,浓度为17%,透明。膜平均流量为1447g/min。 膜前液31.52kg,固含量为4.6%,粘稠,不透明。 Xylose mother liquor fermentation broth 502kg, concentration 17.8%, temperature 34°C, filtration pressure 0.1~0.3MPa. The pore size of the membrane used is 100,000Da. After passing through the membrane equipment, 466.144kg of filtrate is obtained, the concentration is 17%, and it is transparent. The membrane average flow rate is 1447g/min. The pre-membrane solution is 31.52kg, with a solid content of 4.6%, viscous and opaque.
实施例5: Example 5:
分别取膜滤液和发酵离心清液100mL,浓度为21.5%,加入2g活性炭,于55~60℃保温40min,用滤纸过滤。截止过滤时间为16min,测定膜滤液和发酵离心清液体积,其中膜滤液85 mL,发酵离心清液41 mL,过滤效率替提升了一倍左右。 Take 100mL of membrane filtrate and fermentation centrifuge liquid respectively, the concentration is 21.5%, add 2g of activated carbon, incubate at 55~60℃ for 40min, and filter with filter paper. The cut-off filtration time was 16 minutes, and the volumes of the membrane filtrate and the fermentation supernatant were measured. The membrane filtrate was 85 mL, and the fermentation supernatant was 41 mL. The filtration efficiency was about doubled.
Claims (5)
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN201210056432.5A CN102603814B (en) | 2012-03-06 | 2012-03-06 | Method for increasing crystalizing efficiency of xylose in xylose mother solution |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN201210056432.5A CN102603814B (en) | 2012-03-06 | 2012-03-06 | Method for increasing crystalizing efficiency of xylose in xylose mother solution |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CN102603814A CN102603814A (en) | 2012-07-25 |
| CN102603814B true CN102603814B (en) | 2015-01-07 |
Family
ID=46521636
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN201210056432.5A Expired - Fee Related CN102603814B (en) | 2012-03-06 | 2012-03-06 | Method for increasing crystalizing efficiency of xylose in xylose mother solution |
Country Status (1)
| Country | Link |
|---|---|
| CN (1) | CN102603814B (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2023116302A1 (en) | 2021-12-26 | 2023-06-29 | 浙江华康药业股份有限公司 | Method for co-producing erythritol and arabinose from xylose mother liquor |
Families Citing this family (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN103012506A (en) * | 2012-09-07 | 2013-04-03 | 山东绿健生物技术有限公司 | Energy-saving process for extracting crystallized xylose and arabinose from xylose mother liquor |
| CN106946691A (en) * | 2017-03-31 | 2017-07-14 | 山东福洋生物科技有限公司 | A kind of method for reclaiming fermented product in fermented product mother liquor |
| CN109880861A (en) * | 2019-03-06 | 2019-06-14 | 四川金象赛瑞化工股份有限公司 | A kind of method that xylose mother liquid continuously produces furfural |
| CN112480185B (en) * | 2020-11-09 | 2024-02-09 | 河南豫鑫糖醇有限公司 | Process for extracting xylose by biological method |
Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN101643752A (en) * | 2009-06-26 | 2010-02-10 | 安徽丰原发酵技术工程研究有限公司 | Method for producing xylitol and L-arabinose by xylose mother liquor |
| CN101857523A (en) * | 2010-06-07 | 2010-10-13 | 禹城绿健生物技术有限公司 | Method for producing xylitol and arabitol simultaneously by utilizing xylose mother liquid |
-
2012
- 2012-03-06 CN CN201210056432.5A patent/CN102603814B/en not_active Expired - Fee Related
Patent Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN101643752A (en) * | 2009-06-26 | 2010-02-10 | 安徽丰原发酵技术工程研究有限公司 | Method for producing xylitol and L-arabinose by xylose mother liquor |
| CN101857523A (en) * | 2010-06-07 | 2010-10-13 | 禹城绿健生物技术有限公司 | Method for producing xylitol and arabitol simultaneously by utilizing xylose mother liquid |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2023116302A1 (en) | 2021-12-26 | 2023-06-29 | 浙江华康药业股份有限公司 | Method for co-producing erythritol and arabinose from xylose mother liquor |
| US11866756B2 (en) | 2021-12-26 | 2024-01-09 | Zhejiang Huakang Pharmaceutical Co., Ltd. | Methods for co-producing erythritol and arabinose by using xylose mother liquor |
Also Published As
| Publication number | Publication date |
|---|---|
| CN102603814A (en) | 2012-07-25 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US11555049B2 (en) | Method for separation and purification of n-acetylglucosamine | |
| CN101863822B (en) | Production method for extracting tryptophan from fermentation liquor by one-step refining | |
| CN106188167B (en) | A method of separation and Extraction N- acetyl group-D- Glucosamine and D- Glucosamine from ammonia sugar fermentation liquid | |
| CN102603814B (en) | Method for increasing crystalizing efficiency of xylose in xylose mother solution | |
| CN101550101A (en) | Method for clean purifying L-tryptophan by utilizing fermented liquid | |
| CN101085734A (en) | Method for purifying itaconic acid fermentation liquor or extracting itaconic acid from itaconic acid mother liquid by film device | |
| CN105646193A (en) | Method used for separating and extracting lactic acid from fermentation broth | |
| CN106544372A (en) | A kind of method that gamma aminobutyric acid is purified from zymotic fluid | |
| CN112778149A (en) | Method for extracting and separating beta-alanine from fermentation liquor | |
| CN102978250A (en) | Method for producing Gamma-aminobutyric acid through centrifugal mother liquid of glutamic acid | |
| CN101928736A (en) | A kind of separation and purification process of gamma-aminobutyric acid | |
| CN105017360A (en) | Vitamin B12 preparation method | |
| CN111039808A (en) | A kind of method for extracting tyrosine from fermentation broth | |
| CN102676606A (en) | Process for clarifying and removing impurities from fermentation liquor of xylose mother liquid | |
| CN101654413A (en) | Method for extracting and separating L-isoleucine employing three-stage film cascade | |
| US11274122B2 (en) | Separation of enzymes from Trichoderma reesei by filter press and tangential filtration on a ceramic membrane | |
| CN102241707A (en) | Method for extracting L-arabinose and preparing xylitol | |
| CN109678743B (en) | A kind of isolation and purification method of Valine | |
| CN103130664A (en) | Process method of extracting gamma-aminobutyric acid through membrane separation technique | |
| CN102476989B (en) | Succinic acid separating apparatus and method based on full membrane separation system | |
| CN104278071B (en) | The extracting method of cephalosporin | |
| CN112694413A (en) | Method for extracting L-homoserine from fermentation liquor | |
| CN105622342B (en) | A kind of method for detaching 2,3- butanediols | |
| CN103468753A (en) | Water saving method in process of producing sodium gluconate through aspergillus niger fermentation | |
| CN106518700A (en) | Glutamicacid membrane method production process |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| C06 | Publication | ||
| PB01 | Publication | ||
| C53 | Correction of patent of invention or patent application | ||
| CB03 | Change of inventor or designer information |
Inventor after: Yu Li Inventor after: Xin Cheng Xin Inventor after: Jing Wenli Inventor after: Liu Hailiang Inventor before: Xin Cheng Xin Inventor before: Jing Wenli Inventor before: Liu Hailiang |
|
| COR | Change of bibliographic data |
Free format text: CORRECT: INVENTOR; FROM: XIN CHENGFU JING WENLI LIU HAILIANG TO: YU LI XIN CHENGFU JING WENLI LIU HAILIANG |
|
| C10 | Entry into substantive examination | ||
| SE01 | Entry into force of request for substantive examination | ||
| C14 | Grant of patent or utility model | ||
| GR01 | Patent grant | ||
| CF01 | Termination of patent right due to non-payment of annual fee |
Granted publication date: 20150107 |
|
| CF01 | Termination of patent right due to non-payment of annual fee |