CN107183312B - Method for promoting drying and dehydration of potato pulp and application thereof - Google Patents
Method for promoting drying and dehydration of potato pulp and application thereof Download PDFInfo
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- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23K—FODDER
- A23K10/00—Animal feeding-stuffs
- A23K10/30—Animal feeding-stuffs from material of plant origin, e.g. roots, seeds or hay; from material of fungal origin, e.g. mushrooms
- A23K10/37—Animal feeding-stuffs from material of plant origin, e.g. roots, seeds or hay; from material of fungal origin, e.g. mushrooms from waste material
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- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23K—FODDER
- A23K10/00—Animal feeding-stuffs
- A23K10/10—Animal feeding-stuffs obtained by microbiological or biochemical processes
- A23K10/12—Animal feeding-stuffs obtained by microbiological or biochemical processes by fermentation of natural products, e.g. of vegetable material, animal waste material or biomass
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- A—HUMAN NECESSITIES
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- A23K10/00—Animal feeding-stuffs
- A23K10/10—Animal feeding-stuffs obtained by microbiological or biochemical processes
- A23K10/14—Pretreatment of feeding-stuffs with enzymes
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- A—HUMAN NECESSITIES
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- A23V2400/169—Plantarum
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- Y02P60/00—Technologies relating to agriculture, livestock or agroalimentary industries
- Y02P60/80—Food processing, e.g. use of renewable energies or variable speed drives in handling, conveying or stacking
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Abstract
本发明公开了一种促进马铃薯渣干燥脱水的方法及其应用,属于生物质资源利用领域。本发明以鲜马铃薯渣为发酵底物,添加果胶酶、纤维素酶、半纤维素酶中的至少一种进行酶解处理,并接种植物乳杆菌和酵母菌混合菌液,固态厌氧发酵,可以有效防止马铃薯渣腐败变质,改善马铃薯渣的营养价值,并使得马铃薯渣快速脱水,容易干燥,具有较好的经济和环境效益。
The invention discloses a method for promoting drying and dehydration of potato residues and an application thereof, belonging to the field of biomass resource utilization. In the present invention, fresh potato residue is used as fermentation substrate, at least one of pectinase, cellulase and hemicellulase is added to carry out enzymolysis treatment, and mixed bacterial liquid of Lactobacillus plantarum and yeast is inoculated, and solid-state anaerobic fermentation is carried out. , can effectively prevent the potato dregs from spoilage, improve the nutritional value of the potato dregs, and make the potato dregs quickly dehydrate, easy to dry, and have good economic and environmental benefits.
Description
技术领域technical field
本发明涉及一种促进马铃薯渣干燥脱水的方法及其应用,属于生物质资源利用领域。The invention relates to a method for promoting drying and dehydration of potato residues and application thereof, and belongs to the field of biomass resource utilization.
背景技术Background technique
中国的马铃薯种植面积和总产量位居世界首位,每年有大量的马铃薯用于淀粉和全粉的加工。在生产马铃薯淀粉的过程中,产生了大量的废弃物马铃薯渣,平均每生产1吨马铃薯淀粉约产生6~7吨的马铃薯渣。随着马铃薯淀粉产业的迅速发展,马铃薯渣不能得到良好的综合利用问题已经成为制约马铃薯淀粉加工行业发展的瓶颈问题。China's potato planting area and total output ranks first in the world, and a large amount of potato is used for starch and whole flour processing every year. In the process of producing potato starch, a large amount of waste potato dregs is produced, and about 6-7 tons of potato dregs are produced for every 1 ton of potato starch produced on average. With the rapid development of potato starch industry, the problem that potato residue cannot be well utilized has become a bottleneck problem restricting the development of potato starch processing industry.
马铃薯渣主要由水、细胞碎片和残余淀粉颗粒组成。鲜马铃薯渣的含水量可达90%,同时还有纤维素、半纤维素和果胶等持水力较强的物质,使得薯渣不易干燥,干燥成本高,并且马铃薯渣自带33种菌:28种细菌、4种霉菌、1种酵母菌,导致马铃薯渣不易储存、运输,容易腐败变质,产生不良气味。薯渣的转化利用和增效问题得不到解决,容易堆积腐败,造成环境问题,给企业带来困扰与损失。马铃薯渣的日产量巨大,目前对于马铃薯渣的研究仍停留在小批量的实验研究,仍无法解决防腐以及快速脱水干燥而造成马铃薯渣的堆积腐败,因此,如何快速高效的处理马铃薯渣,抑制马铃薯渣中腐败菌的生长,降低马铃薯渣持水力,实现马铃薯渣快速脱水,降低干燥成本的同时提高马铃薯渣的营养价值,成为了一个亟待解决的问题。Potato residue is mainly composed of water, cell debris and residual starch granules. The water content of fresh potato dregs can reach 90%, and there are also substances with strong water holding capacity such as cellulose, hemicellulose and pectin, which make the potato dregs not easy to dry, and the drying cost is high, and the potato dregs come with 33 kinds of bacteria: 28 kinds of bacteria, 4 kinds of molds, and 1 kind of yeast make potato dregs difficult to store and transport, easy to spoil, and produce bad smell. The transformation, utilization and efficiency improvement of potato residues cannot be solved, and it is easy to accumulate corruption, cause environmental problems, and bring trouble and losses to enterprises. The daily output of potato dregs is huge. At present, the research on potato dregs is still in small batch experimental research, and it is still impossible to solve the accumulation and corruption of potato dregs caused by anti-corrosion and rapid dehydration and drying. The growth of spoilage bacteria in the dregs, reducing the water holding capacity of potato dregs, realizing rapid dehydration of potato dregs, reducing drying costs and improving the nutritional value of potato dregs have become an urgent problem to be solved.
发明内容SUMMARY OF THE INVENTION
本发明要解决的技术问题是提供一种抑制马铃薯渣中杂菌生长、提升马铃薯渣品质并实现快速脱水干燥的方法,可以有效防止马铃薯渣腐败变质,改善马铃薯渣的营养价值,并使得马铃薯渣快速脱水,容易干燥,具有较好的经济和环境效益。The technical problem to be solved by the present invention is to provide a method for inhibiting the growth of miscellaneous bacteria in potato dregs, improving the quality of potato dregs and realizing rapid dehydration and drying, which can effectively prevent potato dregs from spoilage, improve the nutritional value of potato dregs, and make potato dregs Rapid dehydration, easy drying, and good economic and environmental benefits.
本发明的第一个目的是提供一种马铃薯渣的发酵方法,所述方法以鲜马铃薯渣为发酵底物,添加果胶酶、纤维素酶、半纤维素酶中的至少一种进行酶解处理,并接种植物乳杆菌和酵母菌混合菌液,固态厌氧发酵。The first object of the present invention is to provide a fermentation method of potato pomace, which uses fresh potato pomace as a fermentation substrate and adds at least one of pectinase, cellulase and hemicellulase to carry out enzymatic hydrolysis Treatment, and inoculated with Lactobacillus plantarum and yeast mixed bacterial liquid, solid-state anaerobic fermentation.
在本发明的一种实施方式中,所述鲜马铃薯渣,水分含量为85~95%。In an embodiment of the present invention, the fresh potato residue has a moisture content of 85-95%.
在本发明的一种实施方式中,所述酶解处理是以果胶酶与纤维素酶以1~3:1~10的比例进行混合,果胶酶以0.25~13U/g的添加量加入鲜马铃薯渣中。In one embodiment of the present invention, the enzymatic hydrolysis treatment is performed by mixing pectinase and cellulase in a ratio of 1-3:1-10, and adding pectinase in an amount of 0.25-13 U/g in fresh potato residue.
在本发明的一种实施方式中,所述酶解处理是以果胶酶与半纤维素酶以1~3:1~5的比例进行混合,果胶酶以0.25~13U/g的添加量加入鲜马铃薯渣中。In one embodiment of the present invention, the enzymatic hydrolysis treatment is performed by mixing pectinase and hemicellulase in a ratio of 1-3:1-5, and adding pectinase in an amount of 0.25-13 U/g Add to fresh potato pulp.
在本发明的一种实施方式中,所述酶解处理是以果胶酶:纤维素酶:半纤维素酶为1~3:1~10:1~5的比例进行混合,果胶酶以0.25~13U/g的添加量加入鲜马铃薯渣中In an embodiment of the present invention, the enzymatic hydrolysis treatment is performed by mixing pectinase: cellulase: hemicellulase in a ratio of 1 to 3: 1 to 10: 1 to 5, and pectinase to The addition amount of 0.25~13U/g is added to the fresh potato residue
在本发明的一种实施方式中,所述固态厌氧发酵后还进行机械脱水和干燥。In an embodiment of the present invention, the solid-state anaerobic fermentation is followed by mechanical dehydration and drying.
在本发明的一种实施方式中,所述接种是以2~14%(菌液体积mL/发酵底物质量g)的接种量接种植物乳杆菌与酵母菌的混合菌液,所述混合菌液的浓度为(1.0~9.9)×109CFU/mL。In one embodiment of the present invention, the inoculation is to inoculate a mixed bacterial solution of Lactobacillus plantarum and yeast with an inoculum amount of 2-14% (volume of bacterial solution mL/mass of fermentation substrate g), and the mixed bacterial solution is The concentration of the solution was (1.0~9.9)×10 9 CFU/mL.
在本发明的一种实施方式中,所述混合菌液中植物乳杆菌与酵母菌的混合比为1~4:1~5In an embodiment of the present invention, the mixing ratio of Lactobacillus plantarum and yeast in the mixed bacterial solution is 1-4:1-5
在本发明的一种实施方式中,所述方法在加入酶液或菌液后进行机械搅拌混合,或采用In one embodiment of the present invention, the method performs mechanical stirring and mixing after adding the enzyme liquid or bacterial liquid, or adopts
均匀喷洒酶和菌种混合液后层铺堆积。Evenly spray the mixture of enzyme and bacterial strains and then lay them up in layers.
在本发明的一种实施方式中,所述发酵采用密封袋、地坑堆积密封或采用密闭发酵罐等装置实现无氧或者厌氧条件。In an embodiment of the present invention, the fermentation adopts a device such as a sealed bag, a pit stacking seal, or a closed fermenter to achieve anaerobic or anaerobic conditions.
在本发明的一种实施方式中,所述发酵温度为25~39℃,发酵时间为48~120h。In an embodiment of the present invention, the fermentation temperature is 25-39° C., and the fermentation time is 48-120 h.
在本发明的一种实施方式中,所述脱水方式为板框压滤、螺旋挤压、离心脱水或其组合。In an embodiment of the present invention, the dehydration method is plate and frame filter press, screw extrusion, centrifugal dehydration or a combination thereof.
在本发明的一种实施方式中,所述干燥方式为鼓风干燥、气流干燥、环流干燥、闪蒸干燥或其组合。In one embodiment of the present invention, the drying method is forced air drying, air flow drying, circulation drying, flash drying or a combination thereof.
在本发明的一种实施方式中,所述方法具体包括如下步骤:In one embodiment of the present invention, the method specifically includes the following steps:
(1)以鲜马铃薯渣为发酵底物,调整水分含量为85~95%,(1) Using fresh potato residue as the fermentation substrate, adjusting the moisture content to 85-95%,
(2)将果胶酶或果胶酶与纤维素酶、半纤维素酶的混合酶与发酵底物混合,酶添加量为0.25~13U/g,混合比例为(果胶酶)1-3:(纤维素酶)1-10:(半纤维素酶)1-5,机械搅拌或翻动使其混合均匀后接种植物乳杆菌或植物乳杆菌与高活性酵母菌混合菌液,菌液接种量为2~14%(菌液体积mL/发酵底物质量g),混合菌液比例为(植物乳杆菌)1-4:(高活性酵母菌)1-5。机械搅拌或翻动使其混合均匀,密封袋、地坑堆积密封或密闭发酵罐,实现无氧或者厌氧条件,25~39℃下进行固态厌氧发酵48~120h。(2) Mix pectinase or the mixed enzyme of pectinase, cellulase and hemicellulase with the fermentation substrate, the enzyme addition amount is 0.25-13U/g, and the mixing ratio is (pectinase) 1-3 : (Cellulase) 1-10: (Hemicellulase) 1-5, inoculate Lactobacillus plantarum or Lactobacillus plantarum mixed bacterial liquid with highly active yeast after mechanical stirring or stirring to make it evenly mixed, the amount of bacterial liquid inoculum It is 2-14% (bacteria liquid volume mL/fermentation substrate mass g), and the mixed bacterial liquid ratio is (Lactobacillus plantarum) 1-4: (highly active yeast) 1-5. Mechanical stirring or turning to make it evenly mixed, sealing bags and pits to seal or airtight fermenters to achieve anaerobic or anaerobic conditions, and solid-state anaerobic fermentation at 25-39 °C for 48-120 hours.
(3)发酵结束后,采用板框压滤、螺旋挤压、离心方式实现马铃薯渣的脱水。(3) After the fermentation is completed, the dehydration of potato residue is realized by means of plate and frame filter press, screw extrusion and centrifugation.
(4)脱水后,采用鼓风、气流干燥、环流干燥、闪蒸干燥或其组合方式干燥马铃薯渣。(4) After dehydration, use blast drying, air drying, circulation drying, flash drying or a combination thereof to dry the potato dregs.
有益效果:(1)本发明通过接种混合微生物进行厌氧发酵,结合酶法处理马铃薯渣,以果胶酶为主,纤维素或半纤维素为辅,使微生物生长过程中提供酶解适宜的pH,而酶解的产物为菌种生长提供营养源,使二者相互发挥协同作用,在不额外添加营养物质的基础上,提高鲜马铃薯渣发酵水平。菌种代谢产物丰富了马铃薯渣的营养组成,提高马铃薯渣作为饲料的应用价值,同时增强抑制腐败变质的能力,并且极大程度上使被马铃薯渣结合的水游离出,实现马铃薯渣的快速脱水和高效干燥,干燥120min后含水率低于30%,干燥240min后含水率低于10%。相比提取马铃薯渣中有效成分、青贮饲料等处理,成本优势明显,可以更好的适应我国马铃薯渣的综合利用的现状和需求。Beneficial effects: (1) In the present invention, anaerobic fermentation is carried out by inoculating mixed microorganisms, combined with enzymatic treatment of potato residues, with pectinase as the main ingredient and cellulose or hemicellulose as a supplement, so as to provide suitable enzymes for enzymatic hydrolysis during the growth of microorganisms. pH, and the products of enzymatic hydrolysis provide a nutrient source for the growth of bacteria, so that the two can play a synergistic role with each other, and improve the fermentation level of fresh potato residue without adding additional nutrients. The metabolites of the bacteria enrich the nutritional composition of potato residues, improve the application value of potato residues as feed, and at the same time enhance the ability to inhibit spoilage, and release the water bound by potato residues to a large extent, realizing rapid dehydration of potato residues And efficient drying, the moisture content is less than 30% after drying for 120min, and the moisture content is less than 10% after drying for 240min. Compared with the extraction of effective components and silage from potato residues, the cost advantage is obvious, and it can better adapt to the current situation and needs of comprehensive utilization of potato residues in my country.
(2)本发明的方法以鲜马铃薯渣为发酵底物,可直接处理马铃薯渣,与其它混合麦麸、米糠等原料发酵处理相比,极大地降低了前处理成本和处理难度,并使本发明的方法处理后的马铃薯渣得率提高1.38~1.88倍。(2) The method of the present invention uses fresh potato dregs as a fermentation substrate, and can directly process potato dregs. Compared with other raw material fermentation processes such as mixed wheat bran and rice bran, the pretreatment cost and the processing difficulty are greatly reduced, and the cost of The yield of potato residues treated by the method of the invention is increased by 1.38-1.88 times.
(3)本发明采用酶结合菌种发酵,使酶与微生物发生协同作用,提高发酵水平,菌种代谢产物有益于丰富马铃薯渣的营养组成并抑制马铃薯腐败变质,还能大幅降低鲜马铃薯渣的黏度,增强其脱水能力,降低其处理难度同时实现其快速干燥。(3) The present invention adopts enzyme-combined strain fermentation to synergize enzymes and microorganisms, improve fermentation level, and bacterial strain metabolites are beneficial to enrich the nutritional composition of potato dregs and inhibit potato spoilage, and can also greatly reduce the amount of fresh potato dregs. Viscosity, enhance its dehydration ability, reduce its processing difficulty and achieve its rapid drying.
(4)本发明所述的固态厌氧发酵,可明显提高马铃薯渣作为培养基的发酵效果,缩短发酵周期(60h即有较高的发酵水平),提高马铃薯渣的营养价值,菌种丰富有益的代谢产物有机酸、单细胞蛋白等增加了马铃薯渣应用于饲料的优势。发酵后的马铃薯渣中有机酸含量(尤其乳酸)是相比于未经处理的薯渣提高明显,乳酸含量由0.0012mg/g增加到4.787mg/g,粗蛋白含量增幅达42%,显著丰富了马铃薯渣作为饲料的营养成分。(4) The solid-state anaerobic fermentation of the present invention can obviously improve the fermentation effect of potato dregs as a culture medium, shorten the fermentation period (60h has a higher fermentation level), improve the nutritional value of potato dregs, and the bacterial species are rich and beneficial The metabolites of organic acids, single-cell protein, etc. increase the advantages of potato residues used in feed. The organic acid content (especially lactic acid) in the fermented potato residue is significantly higher than that of the untreated potato residue. The lactic acid content increases from 0.0012mg/g to 4.787mg/g, and the crude protein content increases by 42%, which is significantly richer. Potato dregs as a nutritional component of feed.
附图说明Description of drawings
图1为酶法结合菌种发酵处理、未接种发酵处理和未经任何处理的鲜马铃薯渣常温放置五天后霉变情况;A,对照;B,接种微生物后的马铃薯渣;Fig. 1 is the mildew condition of the fresh potato dregs after being placed at room temperature for five days with enzyme method combined with bacterial strain fermentation treatment, uninoculated fermentation treatment and without any treatment; A, control; B, potato dregs after inoculation with microorganisms;
图2为不同处理方式马铃薯渣含水率和干燥时间的关系;A为果胶酶添加量为0.25U/g,接种4%植物乳杆菌;B为只接种4%植物乳杆菌;C为未经任何处理的马铃薯渣;D为果胶酶添加量3.75U/g、果胶酶:纤维素酶的酶活比为1:1,接种4%植物乳杆菌;E为果胶酶添加量为0.25U/g,果胶酶:纤维素酶:半纤维素酶的酶活比为1:2:3,接种4%植物乳杆菌;F为果胶酶添加量为0.25U/g,果胶酶、纤维素酶的酶活比为1:4;G为马铃薯淀粉;H为微晶纤维素;Figure 2 shows the relationship between the moisture content and drying time of potato residues in different treatments; A is the addition of pectinase of 0.25U/g, inoculated with 4% Lactobacillus plantarum; B is only inoculated with 4% Lactobacillus plantarum; C is without Potato dregs of any treatment; D is the addition amount of pectinase 3.75U/g, the enzyme activity ratio of pectinase:cellulase is 1:1, inoculated with 4% Lactobacillus plantarum; E is the addition amount of pectinase is 0.25 U/g, the enzyme activity ratio of pectinase: cellulase: hemicellulase is 1:2:3, inoculated with 4% Lactobacillus plantarum; F is the addition amount of pectinase is 0.25U/g, pectinase , the enzyme activity ratio of cellulase is 1:4; G is potato starch; H is microcrystalline cellulose;
图3为不同处理方式马铃薯渣干燥速率和含水率的关系;A为果胶酶添加量为0.25U/g,接种4%植物乳杆菌;B为只接种4%植物乳杆菌;C为未经任何处理的马铃薯渣;D为果胶酶添加量3.75U/g、果胶酶:纤维素酶的酶活比为1:1,接种4%植物乳杆菌;E为果胶酶添加量为0.25U/g,果胶酶:纤维素酶:半纤维素酶的酶活比为1:2:3,接种4%植物乳杆菌;F为果胶酶添加量为0.25U/g,果胶酶、纤维素酶的酶活比为1:4;G为马铃薯淀粉;H为微晶纤维素。Figure 3 shows the relationship between the drying rate and moisture content of potato residues in different treatments; A is the amount of pectinase added is 0.25U/g, inoculated with 4% Lactobacillus plantarum; B is only inoculated with 4% Lactobacillus plantarum; C is without Potato dregs of any treatment; D is the addition amount of pectinase 3.75U/g, the enzyme activity ratio of pectinase:cellulase is 1:1, inoculated with 4% Lactobacillus plantarum; E is the addition amount of pectinase is 0.25 U/g, the enzyme activity ratio of pectinase: cellulase: hemicellulase is 1:2:3, inoculated with 4% Lactobacillus plantarum; F is the addition amount of pectinase is 0.25U/g, pectinase , The enzyme activity ratio of cellulase is 1:4; G is potato starch; H is microcrystalline cellulose.
具体实施方式Detailed ways
具体实施方式中的植物乳杆菌为植物乳杆菌CCTCC M 2017138或植物乳杆菌CCFM8661(公开于公开号为CN102586148A的国家发明专利中),酵母为商业化的安琪酱油酵母(鲁氏酵母)。The Lactobacillus plantarum in the specific embodiment is Lactobacillus plantarum CCTCC M 2017138 or Lactobacillus plantarum CCFM8661 (published in the national invention patent with publication number CN102586148A), and the yeast is commercialized Angel soy sauce yeast (Saccharomyces ruckeri).
实施例1Example 1
向鲜马铃薯渣中加入1U/g的果胶酶,并接种菌液浓度为5.6×109CFU/mL的植物乳杆菌CCTCC M 2017138菌液,接种量为10%(菌液体积mL/发酵底物质量g),混合均匀后,37℃下固态厌氧发酵72h。发酵结束后离心脱水,对发酵体系菌落总数测定,并取出一定量的马铃薯渣在常温下观察其霉变情况。以鲜马铃薯渣作为对照,在相同条件(37℃下固态厌氧发酵72h)下培养。Add the pectinase of 1U/g to the fresh potato residue, and inoculate the bacterial liquid of Lactobacillus plantarum CCTCC M 2017138 that the bacterial liquid concentration is 5.6×10 9 CFU/mL, and the inoculation amount is 10% (the bacterial liquid volume mL/fermentation bottom). Material amount g), after mixing evenly, solid-state anaerobic fermentation was carried out at 37°C for 72h. After the fermentation, centrifuge dehydration, the total number of colonies in the fermentation system was determined, and a certain amount of potato residue was taken out to observe the mildew condition at room temperature. Using fresh potato residue as a control, it was cultured under the same conditions (solid-state anaerobic fermentation at 37°C for 72h).
测定结果表1所示,添加果胶酶和植物乳杆菌发酵处理可明显降低鲜马铃薯渣体系中菌落总数,菌落总数由2.20×108降低至3.46×107(至少一个数量级)。未接种的鲜马铃薯渣在常温放置2天后发生部分区域霉变,接种植物乳杆菌发酵的马铃薯渣在放置5天后,仍未出现霉变现象(图1)。As shown in Table 1, the addition of pectinase and Lactobacillus plantarum fermentation treatment can significantly reduce the total number of colonies in the fresh potato residue system, from 2.20×10 8 to 3.46×10 7 (at least one order of magnitude). The uninoculated fresh potato dregs had mildew in some areas after being placed at room temperature for 2 days, and the potato dregs fermented with Lactobacillus plantarum did not appear mildew after being placed for 5 days (Figure 1).
表1鲜马铃薯渣处理前后的体系菌落总数的变化。Table 1 Changes in the total number of colonies in the system before and after the treatment of fresh potato residues.
说明此种处理方式可抑制鲜马铃薯渣体系中其他菌的生长,达到防腐的效果,延长其贮藏期,常温密闭可以存放15天以上,缓解日产量巨大的鲜马铃薯渣的处理的压力。It shows that this treatment method can inhibit the growth of other bacteria in the fresh potato dregs system, achieve the effect of anti-corrosion, prolong its storage period, and can be stored for more than 15 days in a closed room at room temperature, which relieves the pressure of processing fresh potato dregs with huge daily output.
实施例2Example 2
分别向鲜马铃薯渣中加入以下物质:Add the following substances to the fresh potato dregs separately:
(1)混合比例为1:4(酶活比)的果胶酶与纤维素酶混合酶液,;(2)混合比例为1:2:3(酶活比)的果胶酶、纤维酶与半纤维素酶混合酶液,果胶酶添加量为0.25U/g;(3)混合比例为1:1(酶活比)的果胶酶与纤维素酶,果胶酶添加量为3.75U/g;(4)果胶酶添加量为0.25U/g。(1) Mixed enzyme solution of pectinase and cellulase with a mixing ratio of 1:4 (enzyme activity ratio); (2) pectinase and cellulase with a mixing ratio of 1:2:3 (enzyme activity ratio) Mix the enzyme solution with hemicellulase, the amount of pectinase added is 0.25U/g; (3) the mixing ratio of pectinase and cellulase is 1:1 (enzyme activity ratio), the amount of pectinase added is 3.75 U/g; (4) The amount of pectinase added was 0.25 U/g.
(2)将上述酶液与鲜马铃薯渣混合均匀后,分别接种菌液浓度为4.40×109CFU/mL的植物乳杆菌CCFM 8661菌液,接种量4%(菌液体积mL/发酵底物质量g),混合均匀后,铺平,密封袋密封或采用膜封闭。37℃下固态厌氧发酵72h。发酵结束后,离心脱水,采用鼓风干燥方式,测定不同方式处理后马铃薯渣的干燥特性曲线,以马铃薯淀粉和微晶纤维素为对照。(2) after above-mentioned enzyme liquid and fresh potato residue are mixed, inoculation concentration is respectively 4.40 × 10 9 CFU/mL Lactobacillus plantarum CCFM 8661 bacterial liquid, inoculum amount 4% (bacteria liquid volume mL/fermentation substrate mass g), after mixing evenly, spread out, seal the bag or seal it with a film. Solid-state anaerobic fermentation at 37°C for 72h. After fermentation, centrifugal dehydration was used, and blast drying was used to measure the drying characteristic curves of potato residues treated in different ways, with potato starch and microcrystalline cellulose as controls.
结果如图2、图3所示,相比于未经处理的马铃薯渣,酶结合接种植物乳杆菌处理的马铃薯渣干燥特性有明显的改善。在相同干燥条件下(55℃为例),相比未经处理的马铃薯渣,酶法结合菌种处理后的马铃薯渣含水量低,干燥160~240min,酶法结合菌种处理后的马铃薯渣的含水量低于10%,而未经处理和只接种菌种发酵的马铃薯渣干燥240min后仍有高于30%的水分含量。处理后的马铃薯渣干燥时间短,不再具有鲜马铃薯渣的胶状形态,而是具有一定流动性的状态,经脱水后处理,结构松散,可实现气流干燥。酶法结合菌种发酵处理的马铃薯渣的干燥特性优于只接种菌种发酵处理和不经处理的马铃薯渣。The results are shown in Figures 2 and 3. Compared with the untreated potato residue, the drying characteristics of the potato residue treated with enzyme combined with inoculation with Lactobacillus plantarum were significantly improved. Under the same drying conditions (55℃ as an example), compared with the untreated potato residue, the potato residue treated by the enzyme method combined with the bacteria has a lower water content. The moisture content of the potato residue was lower than 10%, while the untreated and only inoculated potato residues still had a moisture content higher than 30% after drying for 240 min. The treated potato dregs have a short drying time, and no longer have the gelatinous form of fresh potato dregs, but have a certain fluidity. The drying characteristics of the potato residue treated by enzymatic method combined with strain fermentation were better than those treated only by inoculation strain fermentation and untreated potato residue.
实施例3Example 3
向鲜马铃薯渣中加入混合比例为1:4的果胶酶和纤维素酶,以果胶酶添加量为0.25U/g,混合均匀,接种植物乳杆菌和高活性酵母菌混合菌液,接种量为6%,植物乳杆菌(CCFM 8661)菌液浓度为3.2×109CFU/mL,高活性酵母菌复水比为40:1(水质量:酵母粉质量),高活性酵母菌活菌数为7.9×107CFU/mL,两种菌种混合比例为1:2(体积比),混合均匀后,铺平,密封袋密封或采用膜封闭。37℃下固态厌氧发酵48h。发酵结束后样品离心脱水后,55℃下鼓风干燥。记录样品干燥时间以及干燥终点水分含量、干燥后得率。结果如图2所示。Add pectinase and cellulase with a mixing ratio of 1:4 to the fresh potato residue, with the amount of pectinase added as 0.25U/g, mix well, inoculate the mixed bacterial liquid of Lactobacillus plantarum and highly active yeast, inoculate The amount is 6%, the concentration of Lactobacillus plantarum (CCFM 8661) is 3.2×10 9 CFU/mL, the rehydration ratio of high-activity yeast is 40:1 (water quality: yeast powder quality), high-activity yeast live bacteria The number is 7.9×10 7 CFU/mL, and the mixing ratio of the two strains is 1:2 (volume ratio). After mixing evenly, it is spread out, sealed in a sealed bag or sealed with a film. Solid-state anaerobic fermentation at 37°C for 48h. After the fermentation, the samples were centrifuged and dehydrated, and then air-dried at 55°C. Record the drying time of the sample, the moisture content at the end of drying, and the yield after drying. The results are shown in Figure 2.
添加酶结合菌种发酵处理鲜马铃薯渣(湿渣,含水量为92%),干燥240min后含水率降到10%。并且本发明的处理方式可以明显降低离心、压滤后马铃薯渣的含水率。干燥后,马铃薯渣有酯香气味,并可作为饲料,增进动物的采食。经过本发明处理后的马铃薯渣含水量为13.4%,物料得率为7.20g/100g。The fresh potato residue (wet residue, moisture content of 92%) was fermented by adding enzymes combined with bacterial strains, and the moisture content was reduced to 10% after drying for 240 min. In addition, the treatment method of the present invention can significantly reduce the moisture content of the potato residue after centrifugation and filter-pressing. After drying, the potato residue has an estery odor and can be used as feed to improve the feeding of animals. The water content of the potato residue treated by the invention is 13.4%, and the material yield is 7.20g/100g.
实施例4Example 4
向鲜马铃薯渣(湿渣,含水量为91%)中加入混合比例为1:3的果胶酶和纤维素酶,果胶酶添加量为3.75U/g,混合均匀,接种浓度为7.4×109CFU/mL的植物乳杆菌和高活性酵母菌混合菌液,混合比例为1:2(体积比),植物乳杆菌(该植物乳杆菌由江南大学生物工程学院提供)接种量为8%(菌液体积mL/发酵底物质量g),混合均匀后,铺平,密封袋密封或采用膜封闭。37℃下固态厌氧发酵48h。将发酵结束后样品板框压滤后气流干燥。干燥10s时间后,所得样品的含水率为12.3%,物料得率为5.29g/100g。Add pectinase and cellulase with a mixing ratio of 1:3 to the fresh potato residue (wet residue, moisture content of 91%), the amount of pectinase added is 3.75U/g, and the mixture is uniform, and the inoculation concentration is 7.4× 10 9 CFU/mL of Lactobacillus plantarum and highly active yeast mixed bacterial solution, the mixing ratio is 1:2 (volume ratio), and the inoculum amount of Lactobacillus plantarum (the Lactobacillus plantarum is provided by the School of Bioengineering, Jiangnan University) is 8% (mL volume of bacterial liquid/mass g of fermentation substrate), after mixing evenly, spread out, seal the bag or seal it with a membrane. Solid-state anaerobic fermentation at 37°C for 48h. After the fermentation, the sample plate frame was press-filtered and air-dried. After drying for 10s, the moisture content of the obtained sample was 12.3%, and the material yield was 5.29g/100g.
实施例5Example 5
向鲜马铃薯渣中加入果胶酶0.25U/g,果胶酶与纤维素酶混合比例为1:1,混合均匀,接种浓度为7.4×109CFU/mL的植物乳杆菌(CCTCC M 2017138)和高活性酵母菌混合菌液,混合比例为1:1(体积比),植物乳杆菌接种量为8%(菌液体积mL/发酵底物质量g),混合均匀后,铺平,密封袋密封或采用膜封闭。37℃下固态厌氧发酵60h。发酵结束取一定量的发酵产物4500rpm离心15min,取上清液测定有机酸含量。取一定量发酵后样品冷冻干燥,测定其粗蛋白含量。Add pectinase 0.25U/g to the fresh potato residue, the mixing ratio of pectinase and cellulase is 1:1, mix evenly, and inoculate Lactobacillus plantarum with a concentration of 7.4×10 9 CFU/mL (CCTCC M 2017138) Mix bacterial liquid with highly active yeast, the mixing ratio is 1:1 (volume ratio), the inoculum amount of Lactobacillus plantarum is 8% (bacteria liquid volume mL/fermentation substrate mass g), after mixing evenly, spread it out and seal the bag Sealed or closed with membrane. Solid-state anaerobic fermentation at 37°C for 60h. After fermentation, a certain amount of fermentation product was centrifuged at 4500 rpm for 15 min, and the supernatant was taken to measure the organic acid content. A certain amount of fermented samples were freeze-dried to determine their crude protein content.
酶法结合菌种发酵处理后马铃薯渣高效液相色谱法定量乳酸测定结果显示,乳酸含量从原薯渣的0.0012mg/g增加到4.787mg/g。粗蛋白含量从9.80%(w/w)增长到13.92%(w/w)。Quantitative lactic acid determination by high performance liquid chromatography in potato residue after enzymatic method combined with strain fermentation showed that the lactic acid content increased from 0.0012mg/g in raw potato residue to 4.787mg/g. Crude protein content increased from 9.80% (w/w) to 13.92% (w/w).
对照例1Comparative Example 1
具体实施方式同实施例4,区别在于,不添加酶或菌种,或只接种菌种进行发酵,或只添加酶进行处理。The specific embodiment is the same as in Example 4, except that no enzyme or strain is added, or only strain is inoculated for fermentation, or only enzyme is added for treatment.
未经处理以及只接种菌体进行发酵处理的马铃薯渣成典型胶状,黏度大,无流动性,不能实现气流干燥。只添加酶处理的马铃薯渣发酵水平降低,有机酸含量仅为酶法结合菌种发酵处理的一半,抑菌性能大大下降,放置5天开始出现明显霉变现象。The untreated potato residue and the fermented potato residue only inoculated with bacterial cells are typical gelatinous, with high viscosity and no fluidity, and cannot be dried by air flow. The fermentation level of the potato residue treated with only enzyme was reduced, the organic acid content was only half of that of the enzyme combined with bacterial strain fermentation treatment, and the antibacterial performance was greatly reduced, and obvious mildew began to appear after 5 days.
对照例2Comparative Example 2
具体实施方式同实施例3,区别在于,果胶酶添加量为13U/g时,样品干燥后,含水率低于10%,产物的得率仅为3.83g/100g。The specific embodiment is the same as Example 3, except that when the amount of pectinase added is 13 U/g, the moisture content of the sample is lower than 10% after drying, and the yield of the product is only 3.83 g/100 g.
虽然本发明已以较佳实施例公开如上,但其并非用以限定本发明,任何熟悉此技术的人,在不脱离本发明的精神和范围内,都可做各种的改动与修饰,因此本发明的保护范围应该以权利要求书所界定的为准。Although the present invention has been disclosed above with preferred embodiments, it is not intended to limit the present invention. Anyone who is familiar with this technology can make various changes and modifications without departing from the spirit and scope of the present invention. Therefore, The protection scope of the present invention should be defined by the claims.
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