CN111374278A - A kind of low-salt fermented sausage and preparation method thereof - Google Patents
A kind of low-salt fermented sausage and preparation method thereof Download PDFInfo
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- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
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Abstract
本发明主要涉及食品发酵领域,具体而言涉及一种低盐发酵香肠及其制作方法。所述发酵剂包括:类植物乳杆菌、凝结芽孢杆菌及模仿葡萄球菌,所述制备原料还包括谷氨酸钙作为代盐剂。本发明运用产细菌素的乳酸菌发酵剂和产凝结素的凝结芽孢杆菌保证产品安全,利用谷氨酸钙代替部分食盐,并通过葡萄球菌及凝结芽孢杆菌发酵剂弥补由于低盐带来的风味损失。经过试验验证比对结果充分体现了本发明所提出的技术方案的优越。The invention mainly relates to the field of food fermentation, in particular to a low-salt fermented sausage and a preparation method thereof. The starter includes: Lactobacillus plantarum, Bacillus coagulans and Staphylococcus mimicus, and the preparation raw material also includes calcium glutamate as a salt substitute. The present invention uses lactic acid bacteria starter that produces bacteriocin and Bacillus coagulans to ensure product safety, uses calcium glutamate to replace part of salt, and uses staphylococcus and Bacillus coagulans starter to make up for the loss of flavor due to low salt . The comparison results through the test verification fully reflect the superiority of the technical solution proposed by the present invention.
Description
技术领域technical field
本发明主要涉及食品发酵领域,具体而言涉及一种低盐发酵香肠及其制作方法。The invention mainly relates to the field of food fermentation, in particular to a low-salt fermented sausage and a preparation method thereof.
背景技术Background technique
随着人们生活水平提高,饮食结构中肉制品所占比例增高,发酵香肠也逐渐因其富含乳酸菌等益生菌受到人们欢迎。有研究显示食用含有活乳酸菌的食品有可能使其定殖人体肠道,帮助形成不利于病原菌生长的环境,协调人体肠道菌群平衡。但由于发酵香肠工艺特性导致其含盐量相对较高,而近年来高血压等心血管疾病发病率持续走高,并有大量证据显示高钠盐饮食与其发病率呈现相关性。故在此现状下,降低肉制品中钠盐含量对现代人健康饮食、健康生活具有重要意义。With the improvement of people's living standards, the proportion of meat products in the diet structure has increased, and fermented sausages have gradually become popular because of their rich probiotics such as lactic acid bacteria. Studies have shown that eating foods containing live lactic acid bacteria may allow them to colonize the human intestine, help to form an environment that is not conducive to the growth of pathogenic bacteria, and coordinate the balance of human intestinal flora. However, due to the technological characteristics of fermented sausage, its salt content is relatively high, and the incidence of cardiovascular diseases such as hypertension has continued to rise in recent years, and there is a large amount of evidence that a high-sodium diet is associated with its incidence. Therefore, under the current situation, reducing the sodium content in meat products is of great significance to modern people's healthy diet and healthy life.
凝结芽孢杆菌是一种兼性厌氧的革兰氏阳性菌,具备同型乳酸发酵能力,可以将糖类分解为L-乳酸,同时菌株本身还可以合成多种氨基酸,又可产生蛋白酶。凝结芽孢杆菌具备耐盐、耐酸能力,在1%-8%食盐溶液中可存活超过四周,在pH 2.42的酸性溶液中存放一年活菌数还可达到106cfu/ml。凝结芽孢杆菌芽孢萌发速度快,可在肠道内快速生长为营养体,定植性较强,还可产生凝结素,对多种致病菌具有杀菌活性。Bacillus coagulans is a facultative anaerobic gram-positive bacterium with homozygous lactic acid fermentation ability, which can decompose sugars into L-lactic acid. At the same time, the strain itself can synthesize various amino acids and produce protease. Bacillus coagulans has salt resistance and acid resistance, and can survive for more than four weeks in a 1%-8% salt solution, and the number of viable bacteria can reach 10 6 cfu/ml for one year in an acidic solution of pH 2.42. The spores of Bacillus coagulans germinate rapidly, and can quickly grow into vegetative bodies in the intestinal tract.
发酵香肠即将绞碎的瘦肉、动物脂肪以及香辛料混合均匀,接入发酵剂后灌入肠衣,在自然或人工控制的条件下成熟而形成具有特殊香味滋味及稳定微生物特性的发酵肉制品,由于发酵剂的接入,使得发酵香肠具有安全性高、成份稳定、营养价值高的特点。Fermented sausage is about mixing minced lean meat, animal fat and spices evenly, adding starter and then filling into casing, and ripening under natural or artificially controlled conditions to form fermented meat products with special flavor and stable microbial characteristics. The access of the starter makes the fermented sausage have the characteristics of high safety, stable ingredients and high nutritional value.
食盐在发酵香肠加工中起到了凸显咸味、增强风味,调节渗透压、降低水分活度、延长保质期,增加盐溶蛋白溶出、改善产品质构等作用,故添加量通常在4.6%左右;此外,发酵香肠中还会添加亚硝酸钠、谷氨酸钠、柠檬酸钠等钠盐提升产品的质构及安全性。已有大量流行病学调查佐证:长期过量摄入钠盐可能会促进甚至引发部分慢性疾病,过多摄入钠离子会使细胞外液(血浆、组织液、淋巴液)离子浓度增加从而导致其容量增加,其中血浆中钠离子升高则会引发高血压、血管壁增厚、管腔狭窄等问题。2010-2012年中国疾病预防控制中心营养与健康所的调查显示,我国18岁以上公民平均盐摄入量为(9.6±0.3)g/d,其中男性平均(10.4±0.4)g/d,女性平均(8.8±0.3)g/d,高于WHO建议小于5g/d的食盐摄入标准及中国居民膳食指南中建议不超过6g/d的摄入量。In the processing of fermented sausages, salt plays a role in highlighting the salty taste, enhancing the flavor, adjusting the osmotic pressure, reducing the water activity, prolonging the shelf life, increasing the dissolution of the salt-soluble protein, and improving the product texture, so the addition amount is usually about 4.6%; , Sodium nitrite, sodium glutamate, sodium citrate and other sodium salts will be added to the fermented sausage to improve the texture and safety of the product. There has been a large number of epidemiological investigations to support: long-term excessive intake of sodium salt may promote or even cause some chronic diseases, excessive intake of sodium ions will increase the ion concentration of extracellular fluid (plasma, tissue fluid, lymph fluid) and lead to its volume. The increase of sodium ions in the plasma will cause problems such as hypertension, thickening of the blood vessel wall, and lumen stenosis. A survey conducted by the Institute of Nutrition and Health of the Chinese Center for Disease Control and Prevention from 2010 to 2012 showed that the average salt intake of citizens over 18 years old in my country was (9.6±0.3) g/d, of which the average was (10.4±0.4) g/d for men and (10.4±0.4) g/d for women. The average was (8.8±0.3) g/d, which was higher than the WHO recommended salt intake standard of less than 5g/d and the recommended intake of no more than 6g/d in the dietary guidelines for Chinese residents.
发明内容SUMMARY OF THE INVENTION
基于上述缺陷,本发明提供了一种新的低盐发酵香肠。Based on the above defects, the present invention provides a new low-salt fermented sausage.
所述低盐发酵香肠,制备原料包括发酵剂,所述发酵剂包括(由如下组分组成)类植物乳杆菌、凝结芽孢杆菌及模仿葡萄球菌。For the low-salt fermented sausage, the preparation raw materials include a starter, and the starter includes (composed of the following components) Lactobacillus plantarum, Bacillus coagulans and Staphylococcus mimeticum.
优选地,所述发酵剂为:类植物乳杆菌、凝结芽孢杆菌及模仿葡萄球菌按照(1-5):(1-2):1比例组成的菌体混合物;优选,类植物乳杆菌、凝结芽孢杆菌及模仿葡萄球菌按照(2-3):(1-2):1比例组成的菌体混合物;最优选,类植物乳杆菌、凝结芽孢杆菌及模仿葡萄球菌按照2:1:1比例组成的菌体混合物。Preferably, the starter is: a bacterial cell mixture composed of Lactobacillus plantarum, Bacillus coagulans and Staphylococcus mimicus in a ratio of (1-5):(1-2):1; Bacillus and Staphylococcus mimicus in a ratio of (2-3):(1-2):1; most preferably, Lactobacillus plantarum, Bacillus coagulans and Staphylococcus mimicus are composed in a ratio of 2:1:1 bacterial mixture.
所述发酵剂的添加量为,每100kg所述肉类原料,发酵剂的活菌数为(0.1-5)X1010cfu。The added amount of the starter is, per 100kg of the meat raw material, the viable bacteria count of the starter is (0.1-5)× 10 10 cfu.
本发明所述类植物乳杆菌可用本领域常规菌种;优选地,所述类植物乳杆菌为植物乳杆菌L-ZS9(Lactobacillus paraplantarum L-ZS9),类植物乳杆菌L-ZS9分离自比例是发酵肉SAUCISSON SECPUR,现保藏于中国普通微生物菌种保藏中心CGMCC,保藏编号为CGMCCNo.11669。The Lactobacillus plantarum of the present invention can be used conventional strains in the art; preferably, the Lactobacillus plantarum L-ZS9 (Lactobacillus paraplantarum L-ZS9), the Lactobacillus plantarum L-ZS9 is isolated from a proportion of The fermented meat SAUCISSON SECPUR is now preserved in the China General Microorganism Culture Collection Center CGMCC, with the preservation number of CGMCC No.11669.
本发明所述模仿葡萄球菌优选选用模仿葡萄球菌L-RG18(Staphylococcussimulans L-RG18),该菌种分离于法国干香肠(Justin Bridou),现已保藏于中国微生物菌种保藏管理委员会普通微生物中心,地址为北京市朝阳区北辰西路1号院3号,保藏日期为2013年9月25日,保藏编号为CGMCC No.8227,分类名为Staphylococcus simulans。The imitative Staphylococcus of the present invention is preferably selected from Staphylococcus simulans L-RG18 (Staphylococcussimulans L-RG18). The address is No. 3, Yard 1, Beichen West Road, Chaoyang District, Beijing.
本发明所述的凝结芽孢杆菌选优选选用凝结芽孢杆菌D-80(Bacillus coagulansD-80),该菌种现已保藏于中国微生物菌种保藏管理委员会普通微生物中心,地址为北京市朝阳区北辰西路1号院3号,保藏日期为1965年1月1日,保藏编号为CGMCC No.1.7,分类名为Bacillus coagulans。Bacillus coagulans D-80 (Bacillus coagulans D-80) is preferably selected for the selection of Bacillus coagulans described in the present invention, and this strain has been preserved in the General Microorganism Center of the China Microorganism Culture Collection Management Committee, and the address is Beichen West, Chaoyang District, Beijing. No. 3, No. 1 Courtyard, Road 1, the preservation date is January 1, 1965, the preservation number is CGMCC No.1.7, and the classification name is Bacillus coagulans.
优选地,本发明所述的低盐发酵香肠,其制备原料还包括谷氨酸钙作为代盐剂;优选地,所述谷氨酸钙的用量占肉类原料总量的0.01-0.2wt%。Preferably, the preparation material of the low-salt fermented sausage of the present invention further comprises calcium glutamate as a salt substitute; preferably, the amount of calcium glutamate used accounts for 0.01-0.2wt% of the total amount of meat raw materials .
本发明针对现代市场需求,采用类植物乳杆菌、凝结芽孢杆菌及木糖葡萄球菌作为发酵剂,谷氨酸钙作为代盐剂,可得到一种重要的益生菌发酵肉制品。Aiming at the modern market demand, the present invention adopts Lactobacillus plantarum, Bacillus coagulans and Staphylococcus xylosus as starter and calcium glutamate as salt substitute to obtain an important probiotic fermented meat product.
本发明所述的低盐发酵香肠,其制备原料还包括:The low-salt fermented sausage of the present invention, its preparation raw material also includes:
肉类原料:猪后尖肉,猪背膘;所述猪后尖肉和所述猪背膘的质量比为(5-8):3;优选为7:3。Meat raw materials: pork shank meat, pig back fat; the mass ratio of the pig shank meat and the pig back fat is (5-8):3; preferably 7:3.
进一步地,为提升风味,所述低盐发酵香肠的制备原料还包括:Further, in order to enhance the flavor, the preparation material of the low-salt fermented sausage also includes:
食盐,黑胡椒粉,白胡椒粉,白酒中的至少一种;At least one of salt, black pepper, white pepper, and white wine;
优选地,所述食盐的添加量是所述肉类原料总量的0.1-1.8wt%,黑胡椒粉的添加量是所述肉类原料总量的0.01-0.13wt%,白胡椒粉的添加量是所述肉类原料总量的0.01-0.21wt%;白酒的添加量是所述肉类原料总量的0.01-0.2wt%。Preferably, the added amount of the salt is 0.1-1.8 wt% of the total amount of the meat raw materials, the added amount of black pepper is 0.01-0.13 wt% of the total amount of the meat raw materials, and the added amount of white pepper powder is The amount is 0.01-0.21 wt % of the total amount of meat raw materials; the added amount of liquor is 0.01-0.2 wt % of the total amount of meat raw materials.
更为优选地,所述食盐的添加量是所述制备原料总量的1.3-1.8wt%。More preferably, the added amount of the common salt is 1.3-1.8 wt% of the total amount of the preparation raw materials.
本发明所述的低盐发酵香肠还包括:The low-salt fermented sausage of the present invention also includes:
食品级葡萄糖,食品级异抗坏血酸钠,食品级亚硝酸钠中的一种或几种;One or more of food grade glucose, food grade sodium erythorbate, food grade sodium nitrite;
优选地,所述食品级葡萄糖的添加量是所述肉类原料总量的0.01-0.3wt%,食品级异抗坏血酸钠的添加量是所述肉类原料总量的0.01-0.04wt%,食品级亚硝酸钠的添加量是所述肉类原料总量的0.01-0.15wt%。Preferably, the added amount of the food-grade glucose is 0.01-0.3 wt % of the total amount of the meat raw materials, the added amount of food-grade sodium erythorbate is 0.01-0.04 wt % of the total amount of the meat raw materials, and the food The added amount of grade sodium nitrite is 0.01-0.15wt% of the total amount of the meat raw materials.
本发明所提供的低盐发酵香肠可经原料前处理、原料肉腌制、拌料、发酵剂接种、灌肠、发酵等步骤进行制备本发明所述的低盐发酵香肠是一种重要的益生菌发酵肉制品。The low-salt fermented sausage provided by the present invention can be prepared through the steps of raw material pretreatment, raw meat pickling, seasoning, starter inoculation, enema, fermentation, etc. The low-salt fermented sausage of the present invention is an important probiotic Fermented meat products.
同时,本发明提供了上述任意一项技术方案所述的低盐发酵香肠的制作方法,使发酵香肠中具有相对于现有发酵香肠有较低的钠盐含量。At the same time, the present invention provides the manufacturing method of the low-salt fermented sausage according to any one of the above technical solutions, so that the fermented sausage has a lower sodium content than the existing fermented sausage.
具体地,所述制作方法包括发酵,所述发酵的条件为:在湿度85%-95%,温度15℃-23℃,发酵25-30天。Specifically, the production method includes fermentation, and the fermentation conditions are as follows: the humidity is 85%-95%, the temperature is 15°C-23°C, and the fermentation is carried out for 25-30 days.
发酵过程中还应注意,pH需维持在4.5及4.5以下。During the fermentation process, it should also be noted that the pH needs to be maintained at 4.5 and below.
本发明所述的制作方法,还包括在发酵前进行接种,所述接种时,接种用的所述发酵剂的浓度为107-108cfu/g。The preparation method of the present invention further comprises inoculation before fermentation, and during the inoculation, the concentration of the starter used for inoculation is 10 7 -10 8 cfu/g.
本领域技术人员可以理解,本发明所述的制作方法具体包括:Those skilled in the art can understand that the manufacturing method of the present invention specifically includes:
(1)将所述制备原料中的肥肉、瘦肉分别进行彻底冷冻,调节肉内微生物环境;解冻瘦肉,去筋、去皮、切小块备用;(1) the fat meat and lean meat in the described preparation raw material are respectively thoroughly frozen, and the microbial environment in the meat is adjusted;
(2)在步骤(1)中所述的小块解冻瘦肉中添加食盐、谷氨酸钙、亚硝酸钠及其他调味料,搅拌均匀后0-4℃冷藏24-48h;(2) adding salt, calcium glutamate, sodium nitrite and other seasonings to the small pieces of thawed lean meat described in the step (1), stirring evenly and refrigerating at 0-4°C for 24-48h;
(3)将步骤(1)中所述冷冻肥肉切细、步骤(2)中腌制瘦肉搅碎后,在低温环境下混合均匀备用;(3) after the frozen fat meat described in the step (1) is chopped into pieces, the pickled lean meat in the step (2) is smashed, and then mixed evenly under a low temperature environment for subsequent use;
(4)所述接种和所述发酵。(4) The inoculation and the fermentation.
本领域技术人员应当理解,在接种和发酵之间,需利用灌肠机将接入发酵剂的肉馅灌入肠衣并扎口,适当排气后再进行发酵的步骤。Those skilled in the art should understand that between inoculation and fermentation, an enema machine needs to be used to fill the meat stuffing with the starter into the casing and tie the mouth, and then proceed to the fermentation step after proper exhaust.
发酵香肠由于制作工艺的特殊性,盐分含量一般较高,若要减少盐分添加,则会引起一系列安全性、感官质构上的问题。本发明主要从发酵剂和食盐代替物入手,运用产细菌素的乳酸菌发酵剂和产凝结素的凝结芽孢杆菌保证产品安全,利用谷氨酸钙代替部分食盐,并通过葡萄球菌及凝结芽孢杆菌发酵剂弥补由于低盐带来的风味损失。经过试验验证比对结果充分体现了本发明所提出的技术方案的优越。Due to the particularity of the production process of fermented sausages, the salt content is generally high. If the addition of salt is to be reduced, it will cause a series of safety and sensory texture problems. The present invention mainly starts from starter and salt substitute, uses lactic acid bacteria starter producing bacteriocin and Bacillus coagulans to ensure product safety, uses calcium glutamate to replace part of salt, and ferments by Staphylococcus and Bacillus coagulans. The agent makes up for the loss of flavor due to low salt. The comparison results through the test verification fully reflect the superiority of the technical solution proposed by the present invention.
本发明的制作过程中,优选地,步骤(4)之前的所有操作均需在0-4℃下完成,避免微生物过度繁殖,保证后续发酵效果。In the production process of the present invention, preferably, all operations before step (4) need to be completed at 0-4° C. to avoid excessive reproduction of microorganisms and ensure the subsequent fermentation effect.
进一步优选地,本发明在制作过程中,在维持0-4℃低温的基础上,步骤(3)中肥肉、瘦肉细化处理及搅拌时还应避免搅拌机长时间运作而引起局部升温,导致肥肉结构破坏脂肪溢出。Further preferably, in the production process of the present invention, on the basis of maintaining a low temperature of 0-4 ° C, in step (3), the fat and lean meat should be refined and stirred to avoid local heating caused by the long-term operation of the mixer, Causes the fat structure to destroy the fat spillage.
进一步优选地,本发明在制作过程中,在维持0-4℃低温的基础上,步骤(4)中筛选发酵剂需以菌株生长特性研究为基础,以对数期生长情况为基础进行扩大培养,并将扩大培养产物进行不少于2次离心,无菌生理盐水洗涤处理后,以107-108cfu/g用于接种。Further preferably, in the production process of the present invention, on the basis of maintaining a low temperature of 0-4 ° C, in step (4), the screening starter needs to be based on the research on the growth characteristics of the strain, and the expansion culture is carried out on the basis of the logarithmic phase growth situation. , and the expanded culture product was centrifuged for no less than 2 times, washed with sterile saline, and used for inoculation at 10 7 -10 8 cfu/g.
本发明提供的低盐发酵香肠具有以下显著的优异性:The low-salt fermented sausage provided by the present invention has the following remarkable excellence:
(1)类植物乳杆菌(Lactobacillus paraplantarum)作为益生菌不仅能为本发明提供强里的产酸能力,且其具备产生细菌素的能力,进一步提升了本发明的安全性。(1) Lactobacillus paraplantarum as a probiotic can not only provide the present invention with strong acid-producing ability, but also have the ability to produce bacteriocin, which further improves the safety of the present invention.
(2)凝结芽孢杆菌(Bacillus coagulans)作为益生菌不仅能为本发明提供一定的产酸能力,还具备产凝结素的能力,同时具备产生多种氨基酸及分解蛋白能力,不仅提升了产品安全性,还在一定程度上帮助补充了产品风味。(2) Bacillus coagulans as a probiotic can not only provide a certain acid-producing ability for the present invention, but also have the ability to produce coagulins, and at the same time have the ability to produce a variety of amino acids and decompose proteins, which not only improves product safety , but also to a certain extent to help supplement the flavor of the product.
(2)模仿葡萄球菌(Staphylococcus xylosus)较强的解脂解蛋白能力为本发明风味的弥补起到了积极作用。(2) The strong lipolytic and proteolytic ability of imitating Staphylococcus xylosus plays a positive role in supplementing the flavor of the present invention.
(3)谷氨酸钙作为谷氨酸盐对本发明风味的弥补起到积极作用,此外谷氨酸钙中的钙离子为降低本发明中水分活度起到促进作用,进一步提升了本发明的安全性及质构优越性。(3) Calcium glutamate plays a positive role in making up the flavor of the present invention as glutamate, and calcium ions in calcium glutamate play a promoting role for reducing water activity in the present invention, which further improves the present invention. Safety and texture superiority.
具体实施方式Detailed ways
以下实施例用于说明本发明,但不用来限制本发明的范围。The following examples are intended to illustrate the present invention, but not to limit the scope of the present invention.
实施例1Example 1
本实施例提供一种低盐发酵香肠,包括如下组分:The present embodiment provides a low-salt fermented sausage, comprising the following components:
其中,所述发酵剂是由类植物乳杆菌L-ZS9、凝结芽孢杆菌D-80及模仿葡萄球菌L-RG18按照2:1:1比例得到的菌体混合物。Wherein, the starter is a bacterial cell mixture obtained from Lactobacillus plantarum L-ZS9, Bacillus coagulans D-80 and Staphylococcus imitate L-RG18 in a ratio of 2:1:1.
实施例2Example 2
本实施例提供一种低盐发酵香肠,包括如下组分:The present embodiment provides a low-salt fermented sausage, comprising the following components:
其中,所述发酵剂是由类植物乳杆菌L-ZS9、凝结芽孢杆菌D-80及模仿葡萄球菌L-RG18按照2:1:1比例得到的菌体混合物。Wherein, the starter is a bacterial cell mixture obtained from Lactobacillus plantarum L-ZS9, Bacillus coagulans D-80 and Staphylococcus imitate L-RG18 in a ratio of 2:1:1.
实施例3Example 3
本实施例提供实施例1所述的低盐发酵香肠的制作方法,具体步骤如下:The present embodiment provides the preparation method of the low-salt fermented sausage described in embodiment 1, and the concrete steps are as follows:
(1)原料肥肉、瘦肉分别进行彻底冷冻,调节肉内微生物环境;解冻瘦肉,去筋、去皮、切小块备用。(1) Thoroughly freeze the raw fat and lean meat separately to adjust the microbial environment in the meat; thaw the lean meat, remove the tendons, peel the skin, and cut it into small pieces for later use.
(2)在步骤(1)中所述的小块解冻瘦肉中添加食盐、谷氨酸钙、亚硝酸钠及其他调味料,搅拌均匀后0-4℃冷藏24-48h;(2) adding salt, calcium glutamate, sodium nitrite and other seasonings to the small pieces of thawed lean meat described in the step (1), stirring evenly and refrigerating at 0-4°C for 24-48h;
(3)将步骤(2)中所述冷冻肥肉切细、步骤(2)中腌制瘦肉搅碎后,在低温环境下混合均匀备用步骤(3)中肥肉、瘦肉细化处理及搅拌时还应避免搅拌机长时间运作而引起局部升温,导致肥肉结构破坏脂肪溢出。(3) after shredding the frozen fat meat described in step (2), and smashing the pickled lean meat in step (2), mix evenly in a low-temperature environment for subsequent use in step (3) to refine the fat meat and lean meat When mixing, it should also avoid local heating caused by the long-term operation of the mixer, resulting in the destruction of the fat structure and the overflow of fat.
(4)将发酵剂活化后,添加至步骤(3)中所述的混合肉馅,接种;(4) after the starter is activated, add to the mixed meat filling described in step (3), inoculate;
(5)利用灌肠机将步骤(4)中接入发酵剂的肉馅灌入肠衣并扎口,适当排气。(5) Use an enema machine to fill the meat stuffing with the starter in step (4) into the casing, tie the mouth, and ventilate properly.
(6)将步骤(5)中制得的香肠在pH需维持在4.5及4.5以下,湿度维持在85%,温度维持在23℃,发酵25天后即得。(6) The pH of the sausage prepared in step (5) should be maintained at 4.5 and below 4.5, the humidity should be maintained at 85%, and the temperature should be maintained at 23° C., and obtained after fermentation for 25 days.
本实施例步骤(6)之前的所有操作均需在0-4℃下完成,避免微生物过度繁殖,保证后续发酵效果。All operations before step (6) of this embodiment need to be completed at 0-4° C. to avoid excessive reproduction of microorganisms and ensure the subsequent fermentation effect.
实施例4Example 4
本实施例提供实施例2所述的低盐发酵香肠的制作方法,具体步骤如下:The present embodiment provides the preparation method of the low-salt fermented sausage described in embodiment 2, and the concrete steps are as follows:
(1)原料肥肉、瘦肉分别进行彻底冷冻,调节肉内微生物环境;解冻瘦肉,去筋、去皮、切小块备用。(1) Thoroughly freeze the raw fat and lean meat separately to adjust the microbial environment in the meat; thaw the lean meat, remove the tendons, peel the skin, and cut it into small pieces for later use.
(2)在步骤(1)中所述的小块解冻瘦肉中添加食盐、谷氨酸钙、亚硝酸钠及其他调味料,搅拌均匀后0-4℃冷藏24-48h;(2) adding salt, calcium glutamate, sodium nitrite and other seasonings to the small pieces of thawed lean meat described in the step (1), stirring evenly and refrigerating at 0-4°C for 24-48h;
(3)将步骤(2)中所述冷冻肥肉切细、步骤(2)中腌制瘦肉搅碎后,在低温环境下混合均匀备用步骤(3)中肥肉、瘦肉细化处理及搅拌时还应避免搅拌机长时间运作而引起局部升温,导致肥肉结构破坏脂肪溢出。(3) after shredding the frozen fat meat described in step (2), and smashing the pickled lean meat in step (2), mix evenly in a low-temperature environment for subsequent use in step (3) to refine the fat meat and lean meat When mixing, it should also avoid local heating caused by the long-term operation of the mixer, resulting in the destruction of the fat structure and the overflow of fat.
(4)将发酵剂活化后,添加至步骤(3)中所述的混合肉馅,接种;(4) after the starter is activated, add to the mixed meat filling described in step (3), inoculate;
(5)利用灌肠机将步骤(4)中接入发酵剂的肉馅灌入肠衣并扎口,适当排气。(5) Use an enema machine to fill the meat stuffing with the starter in step (4) into the casing, tie the mouth, and ventilate properly.
(6)将步骤(5)中制得的香肠在pH需维持在4.5及4.5以下,湿度维持在90%,温度维持在15℃,发酵30天后即得。(6) The pH of the sausage prepared in step (5) should be maintained at 4.5 and below 4.5, the humidity should be maintained at 90%, and the temperature should be maintained at 15° C., and obtained after fermenting for 30 days.
本实施例步骤(6)之前的所有操作均需在0-4℃下完成,避免微生物过度繁殖,保证后续发酵效果。All operations before step (6) of this embodiment need to be completed at 0-4° C. to avoid excessive reproduction of microorganisms and ensure the subsequent fermentation effect.
对比例1Comparative Example 1
本对比例提供一种低盐发酵香肠,配方如下:This comparative example provides a low-salt fermented sausage with the following formula:
其中,所述发酵剂是由丹麦CHR HANSEN公司生产的F-1CN型号商品发酵剂。Wherein, the starter is the F-1CN model commercial starter produced by Denmark CHR HANSEN company.
对比例2Comparative Example 2
本对比例提供一种低盐发酵香肠,包括如下组分:This comparative example provides a low-salt fermented sausage, comprising the following components:
其中,所述发酵剂是由类植物乳杆菌L-ZS9、凝结芽孢杆菌D-80及模仿葡萄球菌L-RG18按照2:1:1比例得到的菌体混合物。Wherein, the starter is a bacterial cell mixture obtained from Lactobacillus plantarum L-ZS9, Bacillus coagulans D-80 and Staphylococcus imitate L-RG18 in a ratio of 2:1:1.
试验例1Test Example 1
本试验例提供低盐发酵香肠制作过程中品质变化及感官分析。This test example provides quality changes and sensory analysis during the production of low-salt fermented sausages.
共设置4组发酵香肠:低盐实验组、低盐对照组,高盐实验组、高盐对照组用于对比,其中低盐组均使用谷氨酸钙进行代盐处理,高盐组不适用谷氨酸钙;实验组均使用本发明所提供的发酵剂进行制作,对照组使用商品发酵剂进行制作。其中,低盐实验组代表实施例3;高盐实验组的配方同对比例2。A total of 4 groups of fermented sausages were set up: the low-salt experimental group, the low-salt control group, the high-salt experimental group, and the high-salt control group for comparison. The low-salt group was treated with calcium glutamate for salt substitution, and the high-salt group was not applicable Calcium glutamate; the experimental group was made with the starter provided by the present invention, and the control group was made with a commercial starter. Among them, the low-salt experimental group represents Example 3; the formula of the high-salt experimental group is the same as that of Comparative Example 2.
相同的条件下,使用实施例5所述的工艺方法制作低盐实验组、低盐对照组、高盐实验组、高盐对照组发酵香肠。Under the same conditions, the low-salt experimental group, the low-salt control group, the high-salt experimental group, and the high-salt control group fermented sausages were prepared using the process method described in Example 5.
经过前处理,将瘦肉、肥肉按照7:3的用量分别深冻24h后,进行切分处理,瘦肉另于0-4℃腌制24h;0-4℃下绞肉并拌馅,接种107-108cfu/g实验组发酵剂,按照说明接种对照组发酵剂后灌肠、排气;0-1天内控制湿度在90%-95%、温度在20℃-23℃,2-30天内控制湿度在85%-89%、温度在15℃-19℃即得到各组的发酵香肠。After pretreatment, the lean meat and fat meat were deep-frozen for 24 hours according to the dosage of 7:3, and then cut into pieces. The lean meat was marinated at 0-4℃ for 24 hours; Inoculate 10 7 -10 8 cfu/g of the starter of the experimental group, and inoculate the starter of the control group according to the instructions after enema and exhaust; within 0-1 days, control the humidity at 90%-95%, temperature at 20℃-23℃, 2- The fermented sausages of each group were obtained by controlling the humidity at 85%-89% and the temperature at 15°C-19°C within 30 days.
1.微生物检测:1. Microbial detection:
于超净台内用灭菌称量纸称取5.00g去肠衣发酵香肠,用灭菌手术剪剪碎后放入装有45ml灭菌生理盐水及20颗灭菌玻璃珠的锥形瓶中,封口后于摇床中200rpm/min,4℃充分震荡10min。静置5min,利用无菌生理盐水于超净台内对提取液进行梯度稀释,分别吸取不同稀释度菌液0.1ml于选择培养基进行涂布,根据不同培养基要求培养相应时间,观察微生物情况并计数。Weigh 5.00 g of fermented sausages without casing in the ultra-clean bench with sterilized weighing paper, cut them into pieces with sterilized surgical scissors, and put them into a conical flask containing 45 ml of sterilized physiological saline and 20 sterilized glass beads. After sealing, shake it in a shaker at 200 rpm/min and 4°C for 10 min. Let stand for 5 minutes, use sterile physiological saline to dilute the extract in the ultra-clean bench, draw 0.1ml of bacterial solutions of different dilutions to the selective medium for coating, and cultivate for corresponding time according to the requirements of different mediums to observe the microorganisms. and count.
经过测量,对于低盐实验组,发酵第25天时,细菌总数为7.41logcfu/g,乳酸菌数为7.38log cfu/g,芽孢杆菌数为7.35log cfu/g,球菌数7.38log cfu/g;After measurement, for the low-salt experimental group, on the 25th day of fermentation, the total number of bacteria was 7.41logcfu/g, the number of lactic acid bacteria was 7.38logcfu/g, the number of bacillus was 7.35logcfu/g, and the number of cocci was 7.38logcfu/g;
对于低盐对照组,发酵第25天时,细菌总数为7.42log cfu/g,乳酸菌数为7.28logcfu/g,芽孢杆菌数为7.32log cfu/g,球菌数为7.36log cfu/g;For the low-salt control group, on the 25th day of fermentation, the total number of bacteria was 7.42 log cfu/g, the number of lactic acid bacteria was 7.28 log cfu/g, the number of bacilli was 7.32 log cfu/g, and the number of cocci was 7.36 log cfu/g;
对于高盐实验组,发酵第25天时,细菌总数为8.19log cfu/g,乳酸菌数为8.09logcfu/g,芽孢杆菌数为8.08log cfu/g,球菌数为8.09log cfu/g;For the high-salt experimental group, on the 25th day of fermentation, the total number of bacteria was 8.19 log cfu/g, the number of lactic acid bacteria was 8.09 log cfu/g, the number of bacilli was 8.08 log cfu/g, and the number of cocci was 8.09 log cfu/g;
对于高盐对照组,发酵第25天时,细菌总数为8.03log cfu/g,乳酸菌数为8.02logcfu/g,芽孢杆菌数为8.06log cfu/g,球菌数为8.02log cfu/g。For the high-salt control group, on day 25 of fermentation, the total number of bacteria was 8.03 log cfu/g, the number of lactic acid bacteria was 8.02 log cfu/g, the number of bacilli was 8.06 log cfu/g, and the number of cocci was 8.02 log cfu/g.
经过多次平行实验,发现,对于低盐实验组,发酵第25天时,细菌总数为7.3-7.9log cfu/g,乳酸菌数为7.1-7.7log cfu/g,凝结芽孢杆菌数为7.2-7.5log cfu/g,球菌数为7.2-7.5log cfu/g;After many parallel experiments, it was found that for the low-salt experimental group, on the 25th day of fermentation, the total number of bacteria was 7.3-7.9log cfu/g, the number of lactic acid bacteria was 7.1-7.7log cfu/g, and the number of Bacillus coagulans was 7.2-7.5log cfu/g, the number of cocci is 7.2-7.5log cfu/g;
对于低盐对照组,发酵第25天时,细菌总数为7.3-8.1log cfu/g,乳酸菌数为7.1-7.5log cfu/g,凝结芽孢杆菌数为7.2-7.6log cfu/g,球菌数为7.2-7.6log cfu/g;For the low-salt control group, on day 25 of fermentation, total bacteria were 7.3-8.1 log cfu/g, lactobacilli were 7.1-7.5 log cfu/g, Bacillus coagulans were 7.2-7.6 log cfu/g, and cocci were 7.2 -7.6log cfu/g;
对于高盐实验组,发酵第25天时,细菌总数为8.1-8.5log cfu/g,乳酸菌数为8.0-8.4log cfu/g,凝结芽孢杆菌数为7.9-8.3og cfu/g,球菌数为7.8-8.4log cfu/g;For the high-salt experimental group, on the 25th day of fermentation, the total number of bacteria was 8.1-8.5 log cfu/g, the number of lactic acid bacteria was 8.0-8.4 log cfu/g, the number of Bacillus coagulans was 7.9-8.3 log cfu/g, and the number of cocci was 7.8 -8.4log cfu/g;
对于高盐对照组,发酵第25天时,细菌总数为8.0-8.4log cfu/g,乳酸菌数为7.9-8.5log cfu/g,凝结芽孢杆菌数为8.0-8.5log cfu/g,球菌数为7.9-8.5log cfu/g。For the high-salt control group, on day 25 of fermentation, total bacteria were 8.0-8.4 log cfu/g, lactic acid bacteria were 7.9-8.5 log cfu/g, Bacillus coagulans were 8.0-8.5 log cfu/g, and cocci were 7.9 -8.5 log cfu/g.
2.挥发性盐基氮TVB-N的检测:2. Detection of volatile base nitrogen TVB-N:
称取2.50g绞碎香肠并加入25ml蒸馏水,剪切均质20s。于摇床充分振摇30min后4500r/min离心3min。用移液枪分别吸取5ml上清液与5ml氧化镁悬浊液于凯氏定氮管中进行蒸馏,以加入5-6滴混合指示剂的10ml硼酸溶液为吸收剂,每组蒸馏5min,用0.010mol/L的盐酸标准溶液滴定吸收液至蓝紫色为滴定终点。以5ml蒸馏水与5ml氧化镁悬浊液作为空白进行滴定。Weigh 2.50g of minced sausage and add 25ml of distilled water, shear and homogenize for 20s. After fully shaking on a shaker for 30 min, centrifuge at 4500 r/min for 3 min. Use a pipette to draw 5ml of supernatant and 5ml of magnesium oxide suspension and distill them in a Kjeldahl tube. Use 10ml of boric acid solution with 5-6 drops of mixed indicator as the absorbent. Distill for 5 minutes in each group. The 0.010mol/L hydrochloric acid standard solution was titrated to absorb the liquid to blue-purple as the titration end point. The titration was carried out with 5 ml of distilled water and 5 ml of magnesium oxide suspension as blank.
滴定结束后通过滴定盐酸消耗体积计算TVB-N含量。After the titration, the TVB-N content was calculated by titrating the consumption volume of hydrochloric acid.
TVB-N(mg/100g)X×14.0037×0.0104×200TVB-N(mg/100g)X×14.0037×0.0104×200
X——滴定用盐酸体积(ml)X——Volume of hydrochloric acid for titration (ml)
实验结果Experimental results
对于低盐实验组,发酵第25天时,TVB-N含量为0-15mg/100g;For the low-salt experimental group, on the 25th day of fermentation, the TVB-N content was 0-15mg/100g;
对于低盐对照组,发酵第25天时,TVB-N含量为0-13mg/100g;For the low-salt control group, the TVB-N content was 0-13mg/100g on the 25th day of fermentation;
对于高盐实验组,发酵第25天时,TVB-N含量为0-25mg/100g;For the high-salt experimental group, on the 25th day of fermentation, the TVB-N content was 0-25mg/100g;
对于高盐对照组,发酵第25天时,TVB-N含量为0-20mg/100g。For the high-salt control group, the TVB-N content was 0-20 mg/100 g on the 25th day of fermentation.
3.pH值的测定:3. Determination of pH value:
根据GB9695.5-88的方法,只需对TVB-N制备的上清液进行测定。According to the method of GB9695.5-88, only the supernatant prepared by TVB-N needs to be measured.
对于低盐实验组,发酵第25天时,pH值为5.92;For the low-salt experimental group, the pH value was 5.92 on the 25th day of fermentation;
对于低盐对照组,发酵第25天时,pH值为6.00;For the low-salt control group, the pH value was 6.00 on the 25th day of fermentation;
对于高盐实验组,发酵第25天时,pH值为6.02;For the high-salt experimental group, the pH value was 6.02 on the 25th day of fermentation;
对于高盐对照组,发酵第25天时,pH值为6.24。For the high-salt control, the pH was 6.24 on day 25 of fermentation.
经过多次平行实验,发现,对于低盐实验组,发酵第25天时,pH值为5.7-6;After many parallel experiments, it was found that for the low-salt experimental group, the pH value was 5.7-6 on the 25th day of fermentation;
对于低盐对照组,发酵第25天时,pH值为5.7-6.2;For the low-salt control group, the pH was 5.7-6.2 on day 25 of fermentation;
对于高盐实验组,发酵第25天时,pH值为6-6.4;For the high-salt experimental group, on the 25th day of fermentation, the pH value was 6-6.4;
对于高盐对照组,发酵第25天时,pH值为6-6.4。For the high salt control, the pH was 6-6.4 on day 25 of fermentation.
4.硫代巴比妥酸还原值TBARS的检测:4. Detection of thiobarbituric acid reduction value TBARS:
取2.50g绞碎的香肠于研钵加入少许石英砂,充分研磨后加入25ml7.5%三氯乙酸,充分震荡25min后以10000g×g离心10min,再取上清液12000g×g离心1min。取5ml离心上清液加入5ml硫代巴比妥酸溶液,另设置5ml蒸馏水加入5ml硫代巴比妥酸溶液为空白,于90℃水浴锅中保温30min。取出后冷却至室温,1000g×g离心1min,在上清液中加入5ml氯仿,摇匀后静置分层,取上清液于532nm及600nm处测定吸光值。测定结束后利用吸光值计算TBARS。Take 2.50g of minced sausage in a mortar and add a little quartz sand, fully grind and add 25ml of 7.5% trichloroacetic acid, fully shake for 25min, centrifuge at 10000g×g for 10min, and then take the supernatant and centrifuge at 12000g×g for 1min. Take 5ml of centrifugation supernatant and add 5ml of thiobarbituric acid solution, set 5ml of distilled water to add 5ml of thiobarbituric acid solution as blank, and keep in a 90°C water bath for 30min. After taking out, cool to room temperature, centrifuge at 1000g × g for 1min, add 5ml of chloroform to the supernatant, shake well and let stand for stratification, take the supernatant and measure the absorbance at 532nm and 600nm. After the measurement, TBARS was calculated using the absorbance value.
A532——532nm处吸光值A 532 —— Absorbance value at 532nm
A600——600nm处吸光值A 600 —— Absorbance value at 600nm
W——样品质量(g)W——Sample mass (g)
对于低盐实验组,发酵第25天时,TBARS值为0.13;For the low-salt experimental group, the TBARS value was 0.13 on the 25th day of fermentation;
对于低盐对照组,发酵第25天时,TBARS值为0.18;For the low-salt control group, the TBARS value was 0.18 on the 25th day of fermentation;
对于高盐实验组,发酵第25天时,TBARS值为0.15;For the high-salt experimental group, the TBARS value was 0.15 on the 25th day of fermentation;
对于高盐对照组,发酵第25天时,TBARS值为0.13。For the high salt control group, the TBARS value was 0.13 on day 25 of fermentation.
经过多次平行实验,发现,对于低盐实验组,发酵第25天时,TBARS值为0.1-0.2;After many parallel experiments, it was found that for the low-salt experimental group, the TBARS value was 0.1-0.2 on the 25th day of fermentation;
对于低盐对照组,发酵第25天时,TBARS值为0.15-0.3;For the low-salt control group, the TBARS value was 0.15-0.3 on the 25th day of fermentation;
对于高盐实验组,发酵第25天时,TBARS值为0.1-0.2;For the high-salt experimental group, on the 25th day of fermentation, the TBARS value was 0.1-0.2;
对于高盐对照组,发酵第25天时,TBARS值为0.1-0.2。For the high-salt control group, the TBARS value was 0.1-0.2 on day 25 of fermentation.
5.色差检验:5. Color difference inspection:
对于低盐实验组,发酵第25天时,L*为7.41,a*为7.38,b*为7.38;For the low-salt experimental group, on the 25th day of fermentation, L* was 7.41, a* was 7.38, and b* was 7.38;
对于低盐对照组,发酵第25天时,L*为7.42,a*为7.28,b*为7.36;For the low-salt control group, on the 25th day of fermentation, L* was 7.42, a* was 7.28, and b* was 7.36;
对于高盐实验组,发酵第25天时,L*为8.19,a*为8.09,b*为8.09;For the high-salt experimental group, on the 25th day of fermentation, L* was 8.19, a* was 8.09, and b* was 8.09;
对于高盐对照组,发酵第25天时,L*为8.03,a*为8.02,b*为8.02。For the high-salt control group, on day 25 of fermentation, L* was 8.03, a* was 8.02, and b* was 8.02.
经过多次平行实验,发现,对于低盐实验组,发酵第25天时,L*为7-7.5,a*为7-7.5,b*为7-7.5;After many parallel experiments, it was found that for the low-salt experimental group, on the 25th day of fermentation, L* was 7-7.5, a* was 7-7.5, and b* was 7-7.5;
对于低盐对照组,发酵第25天时,L*为7-7.5,a*为7-7.5,b*为7-7.5;For the low-salt control group, on the 25th day of fermentation, L* was 7-7.5, a* was 7-7.5, and b* was 7-7.5;
对于高盐实验组,发酵第25天时,L*为8-8.5,a*为8-8.5,b*为8-8.5;For the high-salt experimental group, on the 25th day of fermentation, L* was 8-8.5, a* was 8-8.5, and b* was 8-8.5;
对于高盐对照组,发酵第25天时,L*为8-8.5,a*为8-8.5,b*为8-8.5。For the high salt control group, on day 25 of fermentation, L* was 8-8.5, a* was 8-8.5, and b* was 8-8.5.
6.质构检测:6. Texture testing:
添加了谷氨酸钙的低盐组发产品具备更优越的硬度与咀嚼性,并且在粘性、内聚力、弹性上与未添加谷氨酸钙的高盐组相差不大。The low-salt group hair products with calcium glutamate added have better hardness and chewiness, and the viscosity, cohesion, and elasticity are not much different from those of the high-salt group without calcium glutamate.
7.感官分析:7. Sensory Analysis:
经过规范的感官测评,相对于低盐对照组,高盐实验组、高盐对照组,以及对比例1和2而言,代表本发明的低盐实验组总体接受性最优,在风味上较突出,而且外观更诱人,更加受大众欢迎,普适性较强。After a standardized sensory evaluation, compared with the low-salt control group, the high-salt experimental group, the high-salt control group, and the comparative examples 1 and 2, the low-salt experimental group represented by the present invention has the best overall acceptance, and has a better flavor. Prominent, and the appearance is more attractive, more popular with the public, and strong universality.
试验例2Test Example 2
本试验例提供实施例2所提供的低盐发酵香肠的过程中品质变化。This test example provides in-process quality changes of the low-salt fermented sausage provided in Example 2.
微生物数据、理化性质数据、含量色差数据均同试验例1所述。Microbial data, physicochemical property data, and content color difference data are the same as those described in Test Example 1.
表1、微生物数据:Table 1. Microbial data:
表2、理化性质数据:Table 2. Physical and chemical properties data:
表3、含量色差仪数据:Table 3. Content colorimeter data:
试验例3Test Example 3
本试验例验证本发明所提供的发酵剂的性能验证。This test example verifies the performance verification of the starter provided by the present invention.
具体步骤如下:Specific steps are as follows:
以1%的接种量于超净台内将保存菌液接入无菌MRS或LB液体培养基,37℃培养12h,连续接种3代至菌株活力正常。Inoculate the preserved bacterial liquid into sterile MRS or LB liquid medium at 1% inoculum in the ultra-clean bench, cultivate at 37°C for 12 hours, and inoculate continuously for 3 generations until the bacterial viability is normal.
以1%的接种量于超净台内将活化菌接入若干份无菌MRS或LB液体培养基,37℃分别培养2、4、6、8、10、12、14、16、18、20、24、28、32、36、42、48h,空白MRS或LB液体培养基作为对照,在相应时间点利用分光光度计于600nm波段处测定菌液OD值,同时利用pH计测量相应时间点菌液pH值。所得到的最大OD值越大则表明菌株活力越强;所得到菌液pH值越小则表明菌株产酸能力越强。Inoculate the activated bacteria into several sterile MRS or LB liquid medium in the ultra-clean bench with 1% inoculum, and culture them at 37°C for 2, 4, 6, 8, 10, 12, 14, 16, 18, 20 , 24, 28, 32, 36, 42, 48h, blank MRS or LB liquid medium was used as a control, and the OD value of the bacterial liquid was measured at the 600nm band using a spectrophotometer at the corresponding time point, and the pH meter was used to measure the bacteria at the corresponding time point. liquid pH. The larger the maximum OD value obtained, the stronger the activity of the strain; the smaller the pH value of the obtained bacterial solution, the stronger the acid-producing ability of the strain.
以的1%接种量于超净台内将活化菌分别接入含0、50、100、150mg/kg亚硝酸钠的MRS或LB液体培养基,37℃培养至对数生长期,空白MRS或LB液体培养基作为对照,利用分光光度计于600nm波段处测量不同亚硝酸钠含量下菌株的OD值。所得到的最终OD值越大则说明菌株耐亚硝酸钠能力越强。Inoculate the activated bacteria with 0, 50, 100, 150 mg/kg sodium nitrite in MRS or LB liquid medium containing 0, 50, 100, and 150 mg/kg of sodium nitrite in the ultra-clean bench with 1% of the inoculum, and culture at 37°C to logarithmic growth phase. LB liquid medium was used as a control, and the OD values of the strains under different sodium nitrite contents were measured by spectrophotometer at 600nm wavelength. The larger the final OD value obtained, the stronger the sodium nitrite resistance of the strain.
取筛选后的对数期活化两种发酵剂,分别以107cfu/ml的接入量于模拟肉汤混合培养12、24、36h,空白模拟肉汤作为对照,在相应时间点利用分光光度计于600nm波段处测定菌液OD值,同时利用pH计测量相应时间点菌液pH值并进行革兰氏染色进行镜检。发酵剂菌株均能生长则表示菌株具备复配生产本发明的能力。The two kinds of starters that were activated in log phase after screening were taken and cultured in simulated broth for 12, 24, and 36 h with an access amount of 10 7 cfu/ml. The blank simulated broth was used as a control. Spectrophotometry was used at corresponding time points The OD value of the bacterial solution was measured at the 600 nm wavelength band, and the pH value of the bacterial solution at the corresponding time point was measured with a pH meter, and Gram staining was performed for microscopic examination. If all the starter strains can grow, it means that the strains have the capability of compound production of the present invention.
虽然,上文中已经用一般性说明、具体实施方式及试验,对本发明作了详尽的描述,但在本发明基础上,可以对之作一些修改或改进,这对本领域技术人员而言是显而易见的。因此,在不偏离本发明精神的基础上所做的这些修改或改进,均属于本发明要求保护的范围。Although the present invention has been described in detail above with general description, specific embodiments and tests, some modifications or improvements can be made on the basis of the present invention, which is obvious to those skilled in the art . Therefore, these modifications or improvements made without departing from the spirit of the present invention fall within the scope of the claimed protection of the present invention.
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