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37 results about "MRS agar" patented technology

De Man, Rogosa and Sharpe agar, often abbreviated to MRS, is a selective culture medium designed to favour the luxuriant growth of Lactobacilli for lab study. Developed in 1960, this medium was named for its inventors. It contains sodium acetate, which suppresses the growth of many competing bacteria (although some other Lactobacillales, like Leuconostoc and Pediococcus, may grow). This medium has a clear brown colour.

A Strain of Enterococcus Faecalis for Feed and Its Application

The invention discloses an Enterococcus faecalis strain SBD, of which the collection number is CGMCC No.4848. The strain is a Gram positive strain and is spherical according to observation with microscope, and the strain does not form spores; the strain can well grow on a Mann, Rogosa and Sharpe (MRS) agar plate and can grow into a round, smooth and raised bacterial colony like a grey white dew and with a diameter of 0.5 to 1 millimeter within 48 hours; and the strain can grow in a facultatively anaerobic environment, the growth temperature range is from 10 to 50 DEG C, the optimal growth temperature is 30 to 40 DEG C, and the growth pH value range is from 4 to 10 and the optimal pH value is 6.5. The bacterial preparation made by the strain is nontoxic and safe, can resist gastric juice and cholate, has a strong inhibition effect on various harmful bacteria and can be widely used in livestock breeding industry (by directly adding into daily ration or drinking water of animals) to increase the disease resistance in animals; and the preparation is expected to replace antibiotic for feed purpose and can obviously improve average weight of weaned piglets, reduce a feed-to-meat ratio and improve living environment of livestock and therefore has a bright prospect.
Owner:北京金泰得生物科技股份有限公司

Optimized process method for improving stability of lactic acid bacteria cells

The invention relates to the technical field of lactic acid bacteria, and provides an optimized process method for improving the cell stability of lactic acid bacteria, which comprises the following steps: S1, culturing strains on an improved MRS agar culture medium solid plate, and screening thallus; S2, culturing the thallus seeds obtained in the step S1, then performing fermentation culture, and performing heat stress treatment on the fermentation liquid in the logarithmic later stage of fermentation; S3, centrifuging the fermentation liquid obtained in S2, and collecting bacterial sludge; S4, uniformly mixing the bacterial sludge obtained in S3 with the fermentation supernatant to obtain an emulsion; S5, freeze-drying the emulsion obtained in S4, and collecting bacterial powder; S6, repeating the operations of S1 to S5 on the bacterial powder obtained in S5 for 20-25 times to obtain stable bacterial powder; and S7, continuously culturing, centrifuging, emulsifying and freeze-drying the stable bacterial powder obtained in S6 to obtain final bacterial powder. According to the technical scheme, the problems that in the prior art, the viable count of lactic acid bacteria in the storage process is reduced, and the stability is not high are solved.
Owner:河北一然生物科技股份有限公司

Culture medium for simultaneously counting lactobacillus rhamnosus and lactobacillus acidophilus and application of culture medium

The invention provides a culture medium for simultaneously counting lactobacillus rhamnosus and lactobacillus acidophilus, and application of the culture medium. The culture medium is formed by improving MRS agar through lincomycin hydrochloride, and the culture medium formed by improving MRS agar through lincomycin hydrochloride is initiatively applied to simultaneous counting of lactobacillus rhamnosus and lactobacillus acidophilus. The invention further provides a method for simultaneously counting lactobacillus rhamnosus and lactobacillus acidophilus by utilizing the culture medium. The method comprises the following steps: firstly laying and solidifying the culture medium, so as to obtain a base layer, adding a to-be-tested mixed sample and the culture medium onto the base layer, and performing laying and solidifying, so as to obtain a middle layer; then adding the culture medium to the middle layer, and performing laying and solidifying, so as to obtain a surface layer, ensuring that the base layer, the middle layer and the surface layer form an interlayer flat plate, finally performing anaerobic cultivation on the interlayer flat plate, and counting lactobacillus rhamnosus and lactobacillus acidophilus separately. The method reduces the costs of experiment vessels, experiment reagents and human resources.
Owner:完美(广东)日用品有限公司 +1

Industrial production method for dried sweet potato leaf products

The invention discloses an industrial production method for dried sweet potato leaf products. The method comprises the following operating steps: screening sweet potato leaves, rinsing with clean water, fixing green and protecting green, marinading and fermenting, separating the leaves and size, drying and dewatering. The method is technically characterized by comprising the steps: marinading andfermenting, namely inoculating lactobacillus plantarum onto an MRS agar medium to be activated, and culturing at a temperature of 33-37 DEG C for 2-3 days; inoculating the activated culture onto sweetpotato leaves in a fermentation tank according to an inoculum size of 3%, adding 3% of salt, uniformly stirring, and sealing the fermentation tank, wherein the fermentation temperature is 30-32 DEG C, and the fermentation time is 2-3 days; drying and dewatering, namely performing forced air drying at the temperature of 45-50 DEG C for 4-5 hours. Constitution water of the sweet potato leaves is not damaged as far as possible, and the original physical, chemical and biological properties and shapes invariable are kept unchanged. According to the method disclosed by the invention, the sweet potato leaves subjected to lactic acid fermentation are well flavored, contain favor components such as lactic acid, amino acids, fatty acids and the like, can achieve the effects of removing the own tannic acid and improving the product flavor and palatability, and are convenient to store, transport and sell after drying and dewatering.
Owner:HUNAN TIANXIANG BIOTECHNOLOGY CO LTD

Process for performing frozen separation on lactic acid bacteria and making dry powder

The invention discloses a process for performing frozen separation on lactic acid bacteria and making dry powder. The process comprises the following steps: S1, preparation of sample bacterial liquid: cutting a lactic acid bacteria source sample into pieces, performing grinding, performing transferring into a centrifugal tube filled with 9 mL of sterile water or normal saline, performing shaking by using a vortex or a shaking table, performing uniform mixing for 10-30 minutes, namely diluting 10 <-1 > sample liquid, and continuously diluting the sample to 10 <-3 >, 10 <-4 > and 10 <-5 >; and S2, culture of lactic acid bacteria colonies: respectively sucking 0.2 mL of the 10 <-3 >, 10 <-4 > and 10 <-5 > sample solutions in the step S1, coating an MRS agar culture medium with the sample solutions, performing operating according to three plates in each gradient, and performing culturing for 24-48 hours at the temperature of 37 DEG C to obtain required lactic acid bacteria colonies. According to the invention, the MRS agar culture medium is coated with the bacterial liquid, the MRS agar culture medium contains a specific content of a freeze-drying protective agent compounded by glucose, peptone, a yeast extract and the like, and in addition, a vacuum-nitrogen charging grinding and crushing technology after freeze-drying is combined, so that the freeze-dried powder can be effectively prevented from absorbing moisture in the environment in the crushing process.
Owner:HUNAN AGRICULTURAL UNIV

Method for detecting quantity of bacterium lacticum in mixed probiotic products

The invention discloses a method for detecting quantity of bacterium lacticum in mixed probiotic products. The method comprises the steps of (1) weighing mixed probiotic samples, adding bacteria-freenormal saline, and performing homogenizing; (2) taking sample homogenizing liquid, adding bacteria-free normal saline, and performing sequential and progressive diluting to an appropriate dilution degree; and (3) absorbing formed sample homogenizing liquid having the appropriate dilution degree to a bacteria-free culture dish, pouring an MRS agar culture medium into the culture dish, performing uniform mixing, performing aerobic culture at 35-37 DEG C for 70-72h, and after culture, counting the quantity of all colonies on a flat plate so as to obtain the quantity of bacterium lacticum. According to the method disclosed by the invention, a manner of performing aerobic culture on bacterium lacticum, only bacterium lacticum grow on a counting culture medium, growth of bifidobacteria is restrained, and interference of bifidobacteria on the detection of the quantity of bacterium lacticum is removed, so that the quantity of bacterium lacticum in the mixed probiotic products can be accuratelydetected, effective detection and control of the quantity of viable bacteria in bacterium lacticum in mixed probiotics can be realized, and the method can fill the blank of the detection of the quantity of bacterium lacticum in mixed probiotics containing bifidobacteria and bacterium lacticum.
Owner:BY HEALTH CO LTD
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