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CN1663437A - A kind of bean curd coagulant and preparation method thereof - Google Patents

A kind of bean curd coagulant and preparation method thereof Download PDF

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CN1663437A
CN1663437A CN2005100432025A CN200510043202A CN1663437A CN 1663437 A CN1663437 A CN 1663437A CN 2005100432025 A CN2005100432025 A CN 2005100432025A CN 200510043202 A CN200510043202 A CN 200510043202A CN 1663437 A CN1663437 A CN 1663437A
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fermentation
medium
coagulating agent
tofu
preparation
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宋俊梅
曲静然
王国良
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Qilu University of Technology
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Abstract

The invention provides a bean curd like coagulant and its production process wherein the coagulant is prepared by using one or more kinds of micro-organisms through fermentation with the acidity of 0.5-50g/100g, the ester content is 20-5000mg/100g. The microorganisms can be bacteria, fungus and saccharomycete capable of producing acid and fragrance. The preparation process consists of carrying out mixed fermentation for one or more microorganisms, the fermentation temperature being 8-60 deg. C, the fermentation time being 4-120 hours, concentrating under normal temperature, and drying to obtain the end product.

Description

一种豆腐类凝固剂及其制备方法A kind of bean curd coagulant and preparation method thereof

技术领域technical field

本发明涉及食品,更具体的讲涉及一种豆腐类凝固剂及其制备方法。The invention relates to food, in particular to a bean curd coagulant and a preparation method thereof.

背景技术Background technique

传统使用的豆腐类凝固剂为卤水(有效成分为MgCl2)和石膏(有效成分为CaSO4),这些凝固剂均不是天然品,对人体存在着已知和未知的危害,而且风味差和风味较单调。后有关技术专家发明了内酯豆腐,内酯豆腐较传统豆腐有不少优点,但由于内酯豆腐在加工过程中葡萄糖酸内酯转化为葡萄糖酸,使豆腐带有一定的酸味。近几年有关技术专家发明了营养保健豆腐凝固剂,由15~25的CaCl2、300~400的葡萄糖酸内酯、50~150的银杏粉、250~370的海藻酸钠、100~200的螺旋粉、30~70的葡萄糖酸锌和5~15(均以重量份计)的芦荟粉组成。营养丰富,但仍采用了大量的葡萄糖酸内酯以及CaCl2Traditionally used tofu coagulants are brine (the active ingredient is MgCl 2 ) and gypsum (the active ingredient is CaSO 4 ), these coagulants are not natural products, there are known and unknown hazards to the human body, and the flavor is poor and More monotonous. Later, relevant technical experts invented lactone tofu. Compared with traditional tofu, lactone tofu has many advantages. However, due to the conversion of gluconolactone into gluconic acid during the processing of lactone tofu, the tofu has a certain sour taste. In recent years, relevant technical experts have invented the nutritional and health tofu coagulant, which consists of 15-25 CaCl 2 , 300-400 gluconolactone, 50-150 ginkgo powder, 250-370 sodium alginate, 100-200 It consists of spiral powder, 30-70% of zinc gluconate and 5-15% (all in parts by weight) of aloe vera powder. Nutritious, but still uses a lot of gluconolactone as well as CaCl 2 .

发明内容Contents of the invention

本发明的目的之一是提供一种对人体没有任何危害和具有良好口味的豆腐类凝固剂;目的之二是提供一种成本低、工艺简单的豆腐类凝固剂的制备方法。One of the purposes of the present invention is to provide a bean curd coagulant that has no harm to the human body and has good taste; the second purpose is to provide a method for preparing the tofu coagulant with low cost and simple process.

本发明的目的之一可通过如下技术措施来实现:One of purpose of the present invention can be realized by following technical measures:

该豆腐类凝固剂是采用一种微生物发酵或多种微生物混合发酵后的发酵液为原料制成的酸度为0.5~50g/100g、酯含量为20~5000mg/100g的凝固剂。The bean curd coagulant is a coagulant with an acidity of 0.5-50g/100g and an ester content of 20-5000mg/100g, which is prepared by using a fermented liquid fermented by a microorganism or mixed fermentation of multiple microorganisms as a raw material.

本发明的目的之一还可通过如下技术措施来实现:One of purpose of the present invention can also be realized by following technical measure:

所述的微生物是能够产酸或产生香味成分的细菌、霉菌和酵母菌;所述的细菌是醋酸菌、乳酸菌和己酸菌;所述的霉菌是曲霉和根霉;所述的酵母菌是汉逊酵母、假丝酵母和酿酒酵母。The microorganisms are bacteria, molds and saccharomyces capable of producing acid or flavor components; the bacteria are acetic acid bacteria, lactic acid bacteria and caproic acid bacteria; the molds are Aspergillus and Rhizopus; Saccharomyces, Candida, and Saccharomyces cerevisiae.

本发明的目的之二可通过如下技术措施来实现:Two of the object of the present invention can be realized by following technical measures:

用一种微生物发酵或多种微生物混合发酵,细菌、霉菌、酵母菌的种子培养基分别采用蛋白胨—酵母膏—葡萄糖培养基、马铃薯—葡萄糖培养基、麦芽汁培养基;发酵培养基的组成为糖蜜或淀粉糖、豆饼水解液加水配制或用无毒无害的食品工业废水添加必需的营养成分后使用;一株菌经活化和扩培后,或两株菌分别经活化和扩培后,按1∶0.5-1.5的比例,以5-15%的接种量接入发酵培养基,控制发酵温度为8~60℃,发酵时间为4~120小时,当发酵液的酸度为0.1~10g/100g、酯含量为10~300mg/100g时,得产品。Use one kind of microorganism to ferment or a variety of microorganisms to ferment together. The seed culture medium of bacteria, mold and yeast adopts peptone-yeast extract-glucose medium, potato-glucose medium and wort medium respectively; the composition of the fermentation medium is Add water to molasses or starch sugar, bean cake hydrolyzate or use non-toxic and harmless food industry wastewater to add necessary nutrients; after activation and expansion of one strain of bacteria, or after activation and expansion of two strains of bacteria respectively, According to the ratio of 1:0.5-1.5, insert the fermentation medium with the inoculation amount of 5-15%, control the fermentation temperature to be 8-60°C, and the fermentation time is 4-120 hours. When the acidity of the fermentation liquid is 0.1-10g/ 100g, when the ester content is 10-300mg/100g, the product is obtained.

本发明的目的之二还可通过如下技术措施来实现:Two of the object of the present invention can also be realized by following technical measures:

将所述的产品采用常规浓缩技术浓缩至原体积的1/5-1/20后得浓缩凝固剂;将浓缩凝固剂采用常规干燥技术进行干燥处理,得固体凝固剂。Concentrate the product to 1/5-1/20 of the original volume by conventional concentration techniques to obtain a concentrated coagulant; dry the concentrated coagulant by conventional drying techniques to obtain a solid coagulant.

本发明的培养基按照所属技术领域的常规根据所用微生物的营养需求进行配制,或用无毒无害的食品工业废水添加必需的营养成分后使用。典型的培养基由糖蜜(或淀粉糖)、豆饼水解液、水组成。发酵液根据需要经常规浓缩得浓缩凝固剂,若再采用常规干燥技术进行干燥处理,得固体凝固剂。The culture medium of the present invention is prepared according to the nutritional requirements of the microorganisms used according to the routine in the technical field, or used after adding necessary nutrients with non-toxic and harmless food industry wastewater. A typical medium consists of molasses (or starch sugar), bean cake hydrolyzate, and water. The fermented liquid is conventionally concentrated to obtain a concentrated coagulant as required, and then dried by conventional drying techniques to obtain a solid coagulant.

本发明所述凝固剂的用量为:每凝固1000公斤豆浆,以固体凝固剂计需用5~12公斤。The consumption of coagulant of the present invention is: every 1000 kilograms of soya-bean milks of coagulation need use 5~12 kilograms in terms of solid coagulant.

本发明的使用方法:大豆进行浸泡后,按干豆与水的重量份配比1∶12磨制成豆浆,将豆浆煮沸,冷却至80℃左右时,边搅拌边加入本发明的凝固剂,即得豆脑。再根据不同需要进行后续处理,可得不同豆腐类制品。The use method of the present invention: after soybeans are soaked, grind the soybean milk according to the weight ratio of dry beans and water of 1:12, boil the soybean milk, and when it is cooled to about 80°C, add the coagulant of the present invention while stirring, That is, bean brain. Then follow-up treatment is carried out according to different needs, and different tofu products can be obtained.

本发明的豆腐类凝固剂为纯天然无毒无害的微生物经发酵而成,因而没有任何对人体产生危害的物质而且所凝固的豆腐具有良好的质构和风味。本发明不但产品成本很低,而且制备成本也很低,工艺简单,无任何污染。The bean curd coagulant of the present invention is fermented by pure natural, non-toxic and harmless microorganisms, so there is no substance harmful to the human body, and the coagulated tofu has good texture and flavor. The invention not only has very low product cost, but also has low preparation cost, simple process and no pollution.

具体实施方式Detailed ways

实施例1:Example 1:

用嗜热链球菌和醭膜假丝酵母作为生产菌株。其种子培养基分别为蛋白胨、酵母膏、葡萄糖培养基(蛋白胨12g,酵母膏3g,葡萄糖1g,加水1000mL)和麦芽汁培养基(12Brix)。发酵培养基由豆腐黄浆水加5%葡萄糖配制而成。两株菌分别经活化和扩培后,按1∶1的比例,以5%的接种量接入发酵培养基,40℃温度下发酵120小时,当发酵液的酸度为4g/100g、酯含量10mg/100g时,将发酵液过滤除菌,然后进行减压蒸馏浓缩至原体积的1/10,再经真空浓缩干燥,得固体凝固剂,酸度为50g/100g、酯含量为20mg/100g。Streptococcus thermophilus and Candida hymenophilus were used as production strains. The seed medium is peptone, yeast extract, glucose medium (peptone 12g, yeast extract 3g, glucose 1g, water 1000mL) and wort medium (12Brix). The fermentation medium is prepared by adding 5% glucose to tofu yellow slurry water. After the two strains were respectively activated and expanded, they were inserted into the fermentation medium with an inoculum size of 5% at a ratio of 1:1, and fermented for 120 hours at a temperature of 40°C. When the acidity of the fermentation broth was 4g/100g and the ester content When the concentration is 10mg/100g, filter and sterilize the fermentation broth, then carry out vacuum distillation and concentrate to 1/10 of the original volume, and then concentrate and dry in vacuo to obtain a solid coagulant with an acidity of 50g/100g and an ester content of 20mg/100g.

实施例2:Example 2:

用白膜醋酸菌和酿酒酵母作为生产菌株。其种子培养基分别为葡萄糖—酵母膏—酒精培养基(葡萄糖6g,酵母膏6g,酒精25mL,加水1000mL)和麦芽汁培养基(8Brix)。发酵培养基的组成为淀粉水解液(按葡萄糖终浓度6%)、豆饼水解液(按豆饼粉终浓度1%)加水配制。两株菌分别经活化和扩培后,按1∶1.5的比例,以12%的接种量接入发酵培养基,8℃温度下发酵80小时,当发酵液的酸度为0.1g/100g、酯含量100mg/100g时,将发酵液采用常规机械过滤方式进行过滤并除菌,然后进行减压蒸馏浓缩至原体积的1/8,得浓缩凝固剂,产品酸度为0.5g/100g、酯含量为200mg/100g。Acetobacter albuginea and Saccharomyces cerevisiae were used as production strains. The seed culture medium is glucose-yeast extract-alcohol medium (glucose 6g, yeast extract 6g, alcohol 25mL, water 1000mL) and wort medium (8Brix). The fermentation medium is composed of starch hydrolyzate (6% final concentration of glucose), bean cake hydrolyzate (1% final concentration of bean cake powder) and water. After the two strains were respectively activated and expanded, they were inserted into the fermentation medium at a ratio of 1:1.5 with an inoculum size of 12%, and fermented for 80 hours at a temperature of 8°C. When the acidity of the fermentation liquid was 0.1g/100g, ester When the content is 100mg/100g, the fermentation broth is filtered and sterilized by conventional mechanical filtration, and then concentrated to 1/8 of the original volume by distillation under reduced pressure to obtain a concentrated coagulant. The acidity of the product is 0.5g/100g, and the ester content is 200mg/100g.

实施例3:Example 3:

用乳酸菌和米曲霉作为生产菌株。其种子培养基分别为蛋白胨—酵母膏—葡萄糖培养基(蛋白胨10g,酵母膏3g,葡萄糖2g,加水1000mL)和马铃薯—葡萄糖培养基(马铃薯200g,葡萄糖20g,加水1000mL)。发酵培养基的组成为淀粉糖(按葡萄糖终浓度4%)、豆饼水解液(按豆饼粉终浓度1%)加水配制。两株菌分别经活化和扩培后,按1∶0.5的比例,以15%的接种量接入发酵培养基,60℃温度下发酵4小时,当发酵液的酸度为10g/100g、酯含量120mg/100g时,将发酵液采用常规机械过滤方式进行过滤并除菌,然后进行减压蒸馏浓缩至原体积的1/5,得浓缩凝固剂,产品酸度为40g/100g、酯含量为400mg/100g。Lactic acid bacteria and Aspergillus oryzae were used as production strains. The seed culture medium is peptone-yeast extract-glucose medium (peptone 10g, yeast extract 3g, glucose 2g, water 1000mL) and potato-glucose medium (potato 200g, glucose 20g, water 1000mL). The fermentation medium is composed of starch sugar (4% final concentration of glucose), bean cake hydrolyzate (1% final concentration of bean cake powder) and water. After the two strains were respectively activated and expanded, they were inserted into the fermentation medium at a ratio of 1:0.5 with an inoculum size of 15%, and fermented for 4 hours at a temperature of 60°C. When the acidity of the fermentation broth was 10g/100g and the ester content When the concentration is 120mg/100g, the fermentation liquid is filtered and sterilized by conventional mechanical filtration, and then concentrated to 1/5 of the original volume by vacuum distillation to obtain a concentrated coagulant. The acidity of the product is 40g/100g, and the ester content is 400mg/ 100g.

实施例4:Example 4:

用己酸菌、汉逊酵母作为生产菌株。其种子培养基分别为蛋白胨—酵母膏—葡萄糖培养基(蛋白胨11g,酵母膏7g,葡萄糖1.5g,加水1000mL)和麦芽汁培养基(11Brix)。发酵培养基的组成为糖蜜(按葡萄糖终浓度3%)、豆饼水解液(按豆饼粉终浓度2%)加水配制。两株菌分别经活化和扩培后,按1∶1的比例,以8%的接种量接入发酵培养基,10℃温度下发酵50小时,当发酵液的酸度为1g/100g、酯含量300mg/100g时,进行减压蒸馏浓缩至原体积的1/20,得浓缩凝固剂,产品酸度为30g/100g、酯含量为5000mg/100g。Caproic acid bacteria and Hansenula were used as production strains. The seed culture medium is peptone-yeast extract-glucose medium (peptone 11g, yeast extract 7g, glucose 1.5g, water 1000mL) and wort juice medium (11Brix). The composition of the fermentation medium is prepared by adding water to molasses (according to the final concentration of glucose at 3%), bean cake hydrolyzate (according to the final concentration of bean cake powder at 2%). After the two strains were respectively activated and expanded, they were inserted into the fermentation medium with an inoculum size of 8% at a ratio of 1:1, and fermented for 50 hours at a temperature of 10°C. When the acidity of the fermentation broth was 1g/100g and the ester content When the concentration is 300mg/100g, carry out vacuum distillation and concentrate to 1/20 of the original volume to obtain a concentrated coagulant with an acidity of 30g/100g and an ester content of 5000mg/100g.

实施例5:Example 5:

用黑根霉作为生产菌株。其种子培养基为马铃薯—葡萄糖培养基(马铃薯200g,葡萄糖20g,加水1000mL)。发酵培养基的组成为糖蜜(按葡萄糖终浓度4%)、豆饼水解液(按豆饼粉终浓度2%)加水配制。菌种经活化和扩培后,按1∶0.8的比例,以10%的接种量接入发酵培养基,36℃温度下发酵10小时,当发酵液的酸度为1.2g/100g、酯含量160mg/100g时,得产品,经薄膜浓缩、喷雾干燥得酸度为20g/100g、酯含量为3000mg/100g的固体凝固剂。Rhizopus niger was used as the production strain. The seed medium is potato-glucose medium (200 g of potatoes, 20 g of glucose, and 1000 mL of water). The composition of the fermentation medium is prepared by adding water to molasses (4% final concentration of glucose), bean cake hydrolyzate (2% final concentration of bean cake powder). After the bacterial classification is activated and expanded, it is inserted into the fermentation medium with an inoculum size of 10% according to the ratio of 1:0.8, and fermented for 10 hours at a temperature of 36°C. When the acidity of the fermentation broth is 1.2g/100g and the ester content is 160mg In the time of /100g, obtain product, be that acidity is 20g/100g, ester content is the solid coagulant of 3000mg/100g through thin film concentration, spray drying.

Claims (6)

1, a kind of Tofu coagulating agent, it is characterized in that adopting the zymotic fluid after a kind of microbial fermentation or the multiple microorganism mixed culture fermentation is that the acidity that raw material is made is that 0.5~50g/100g, ester content are the coagulating agent of 20~5000mg/100g.
2, a kind of Tofu coagulating agent according to claim 1 is characterized in that described microorganism is bacterium, mould and the saccharomycete that can produce acid or produce flavor component.
3, a kind of Tofu coagulating agent according to claim 2 is characterized in that described bacterium is acetic acid bacteria, lactic acid bacteria and caproic acid bacteria; Described mould is aspergillus and head mold; Described saccharomycete is Hansenula yeast, Candida and saccharomyces cerevisiae.
4, the preparation method of the Tofu coagulating agent of claim 1, it is characterized in that bacterium, mould, saccharomycetic seed culture medium adopt peptone-yeast extract-dextrose culture-medium, potato-dextrose culture-medium, malt extract medium respectively with a kind of microbial fermentation or multiple microorganism mixed culture fermentation; Fermentation medium consist of that molasses or starch sugar, soya-bean cake hydrolyzate add the water preparation or with using after the essential nutritional labeling of nontoxic food industrial wastewater interpolation; One strain bacterium activated and spread cultivation after, or two the strain bacterium activated respectively and spread cultivation after, in 1: the ratio of 0.5-1.5, inoculum concentration with 5-15% inserts fermentation medium, the control fermentation temperature is 8~60 ℃, fermentation time is 4~120 hours, when the acidity of zymotic fluid be 0.1~10g/100g, when ester content is 10~300mg/100g, product.
5, the preparation method of a kind of Tofu coagulating agent according to claim 4 must concentrate coagulating agent after it is characterized in that adopting conventional concentration technique to be concentrated into the 1/5-1/20 of original volume the described product.
6, the preparation method of a kind of Tofu coagulating agent according to claim 5 is characterized in that adopting the conventional drying technology to carry out drying in concentrated coagulating agent handles, get the solid solidifies agent.
CN2005100432025A 2005-03-30 2005-03-30 A kind of bean curd coagulant and preparation method thereof Pending CN1663437A (en)

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Cited By (10)

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CN102217679A (en) * 2011-06-08 2011-10-19 北京融青生态农业有限公司 Novel ecological bean curd and preparation method of bean curd
CN103202350A (en) * 2013-04-28 2013-07-17 深圳市福荫食品集团有限公司 Tough tofu producing method and tough tofu
CN103416640A (en) * 2012-12-29 2013-12-04 河南工业大学 Method for fermentation production of tofu physalis alkekengi by using lactobacillus amylolyticus
CN104273230A (en) * 2014-05-09 2015-01-14 浙江大学 Sour serofluid for making sauced beancurd and preparation method of sour serofluid
CN106578118A (en) * 2016-11-29 2017-04-26 郭宏君 Bean product coagulator prepared from food, preparation method and bean curd
CN107279311A (en) * 2017-07-26 2017-10-24 湖州老恒和酿造有限公司 A kind of preparation method of feature fermented bean curd
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CN107637666A (en) * 2017-11-08 2018-01-30 广州市妙豆生物科技有限公司 A kind of Kefir grains bean curd coagulant and preparation method thereof
CN110226638A (en) * 2019-07-03 2019-09-13 邵阳学院 One seed oyster bean curd and preparation method thereof
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Cited By (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102217679A (en) * 2011-06-08 2011-10-19 北京融青生态农业有限公司 Novel ecological bean curd and preparation method of bean curd
CN103416640A (en) * 2012-12-29 2013-12-04 河南工业大学 Method for fermentation production of tofu physalis alkekengi by using lactobacillus amylolyticus
CN103202350A (en) * 2013-04-28 2013-07-17 深圳市福荫食品集团有限公司 Tough tofu producing method and tough tofu
CN103202350B (en) * 2013-04-28 2014-04-02 深圳市福荫食品集团有限公司 Tough tofu producing method and tough tofu
CN104273230A (en) * 2014-05-09 2015-01-14 浙江大学 Sour serofluid for making sauced beancurd and preparation method of sour serofluid
CN106578118A (en) * 2016-11-29 2017-04-26 郭宏君 Bean product coagulator prepared from food, preparation method and bean curd
CN107279311A (en) * 2017-07-26 2017-10-24 湖州老恒和酿造有限公司 A kind of preparation method of feature fermented bean curd
CN107593932A (en) * 2017-11-08 2018-01-19 广州市妙豆生物科技有限公司 A kind of water Kefir grains bean curd coagulant and preparation method thereof
CN107637666A (en) * 2017-11-08 2018-01-30 广州市妙豆生物科技有限公司 A kind of Kefir grains bean curd coagulant and preparation method thereof
CN110226638A (en) * 2019-07-03 2019-09-13 邵阳学院 One seed oyster bean curd and preparation method thereof
CN110403019A (en) * 2019-07-03 2019-11-05 邵阳学院 A kind of scallop tofu and preparation method thereof

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