31 results about "Botryosphaeria rhodina" patented technology

The invention provides a method for producing fermented beef jerky with compound leaven. The bacteria strain used in fermentation is lactobacillus casei and staphylococcus xylosus with volume ratio of 1:3 and volume of addition of 1-1.5%, the fermentation temperature is 20 DEG C, and the fermentation time is 5 days. The addition of lactobacillus casei reduces pH value of the product, improves safety, improves the texture of the product, and shortens fermentation period. At the same time, the addition of staphylococcus xylosus generates a large amount of flavoring substances during fermentation process, improves sensing effect of the product, and the final product has thick fragrance, good taste, and infinitive aftertaste. The inventive method is especially suitable for producing fermented beef jerky, as well as air dried sausage and sausage.

A crystalline form of crystalline (R)-3-(4-(2-(2-methyltetrazol-5-yl)-pyridin-5-yl)-3-fluorophenyl)-5-hydroxymethyl oxazolidin-2-one dihydrogen phosphate, methods of making the crystalline form and pharmaceutical compositions comprising the crystalline form are useful antibiotics. Further, the derivatives of the present invention may exert potent antibacterial activity versus various human and animal pathogens, including Gram-positive bacteria such as Staphylococi, Enterococci and Streptococi, anaerobic microorganisms such as Bacteroides and Clostridia, and acid-resistant microorganisms such as Mycobacterium tuberculosis and Mycobacterium avium. Accordingly, the compositions comprising the crystalline form may be used in antibiotics.

The invention discloses a method for manually inducing Aquilaria sinensis to generate agilawood. The method comprises the following steps of: injecting a methanoic acid or acetic acid solution with pH value of 1.5-3 or a mixed solution of methanoic acid and acetic acid into xylem of Aquilaria sinensis [Aquilaria sinensis (Lour.) Gilg]; respectively injecting the solution together with fungi, suchas Botryosphaeria rhodina, Hypocrea jecorina, Fusarium sp., Colletotrichum gloeosporioides, Ampelomyces sp, Khuskia sp, Fungal endophyte sp.A 16, Pestalotiopsis sp., Hypocrea lixii and Chaetomium sp.or injecting the solution and the fungi in a mixed way; and inducing the Aquilaria sinensis to generate the agilawood. According to the invention, the methanoic acid or acetic acid solution or the mixed solution of methanoic acid and acetic acid is injected into the xylem of the Aquilaria sinensis to induce the Aquilaria sinensis to generate defense reaction so as to generate the agilawood; and alarge amount of agilawood are generated by using the method. The method for manually inducing the Aquilaria sinensis to generate the agilawood, disclosed by the invention, has the advantages of simplicity and convenience in operation, low cost and suitability for manually making agilawood on a large scale by using Aquilaria sinensis trees; and a large amount of agilawood can be effectively generated by the Aquilaria sinensis. According to the invention, the agilawood producing period of the Aquilaria sinensis is largely reduced, the agilawood can be generally obtained after 6-24 months, the production cost is reduced, the market requirements are satisfied, and important economic, social and ecological benefits are obtained in aspects of protection and sustainable utilization of the Aquilaria sinensis, economic development of mountainous regions and the like.

The present invention provides a method of detecting thermonuclease-positive staphylococci that does not require inactivation of DNase-positive/TNase-negative bacteria with heat. The method includes (a) providing a culture medium selective for growing staphylococci; (b) inoculating the culture medium with a sample; (c) incubating the inoculated culture medium under conditions effective to promote the growth of staphylococci; (d) providing an indicator system that produces a differentiable, detectable signal in the presence of thermonuclease-positive staphylococci; (e) contacting the indicator system with the inoculated, incubated culture medium, thereby forming a detection assembly; (f) incubating the detection assembly under conditions effective for generating the differentiable, detectable signal; and (g) detecting the detectable signal.

The present invention also provides a culture medium for the selective identification of Staphylococcus aureus. The culture medium includes at least one first selective agent that selects for growth of staphylococci; at least one second selective agent for differentiating Staphylococcus aureus from other staphylococci; at least one first indicator for indicating the presence of staphylococci; and at least one second indicator for differentially indicating the presence of non-staphylococci bacteria. The present invention also provides a method of selectively identifying Staphylococcus aureus in a sample by using the culture medium of the present invention.

The invention relates to a 3-carbonyl-6-ethoxycarbonyl-thiazole pyrimidine compound and a synthesis method and application thereof. The compound has a right structure formula. The 3-carbonyl-6-ethoxycarbonyl-thiazole pyrimidine compound serving as an inhibiting agent of YyCG histidine kinase protein for a staphylococcus epidermidis signal transduction system has a novel structure, and the adopted method for preparing the compound is simple and easy to implement. The test results of the minimal inhibitory concentration (MIC) and the minimal bactericidal concentration (MBC) show that the compound has excellent inhibitory action on the formation of a staphylococcal biological film and can effectively kill and wound the bacteria in the staphylococcal biological film.

The invention provides primers designed on base of the difference of sequences among staphylococcal enterotoxin subtypes, i.e., C₁, C₂ and C₃. The invention also provides a PCR method for detecting subtypes of staphylococcal enterotoxin type C by using the above-mentioned primers. The invention relates also to DNA probes useful for the identification of subtypes C₁, C₂ and C₃ of staphylococcal enterotoxin type C in various food and clinical samples. The primers of the invention comprises following sequences:

Methods for producing cyclic polypeptides comprising a lactone or thiolactone ring. In certain cases, intein fusion proteins may be used in a method for biologically producing internally cyclized polypeptides. The new methods enable the construction of cyclic polypeptide libraries that may be screened for the biological activity of cyclic polypeptides. Methods provided may be used, for instance, to produce and optimize novel cyclic peptides for use in treating Staphylococcal infections.

The invention relates to functional polypeptides secreted from Botryospaeria rhodina CBS 247.96.

The invention relates to a skin care composition which contains 0.01-1 percent by mass of lysostaphin and 5-10 percent by mass of Chinese herbal extracts, wherein the Chinese herbal extracts include at least one of a mint extract, a honeysuckle extract, a houttuynia cordata extract and a groundsel extract. The skin care composition has a function of preventing and removing prickly heat, does not contain powder carriers and has no damage to the organisms. The invention also provides a paper towel comprising the skin care composition and a preparation method of the paper towel.

The invention relates to Staphylococcus epidermidis CGMCC 3472 and application thereof in producing fermented segmental pork. The mouthfeel and other qualities of pork blocks of the fermented segmental pork produced by the strain approach or are superior to those of naturally-fermented hams; in addition, the fermented segmental pork has short production period and can be manufactured into small packages; meanwhile, the quality stability of products can be improved.

The invention discloses a detection method of main spoilage microorganism in tomato paste and aims at no report about the detection method of main spoilage microorganism in tomato paste at home and abroad. The method is carried out as follows: by adopting the pre-breeding cultivation, the 8 to 12 percent by weight in volume of tomato paste is taken, and physiological saline of 200 to 250 mililiter is added into the tomato paste and well-mixed to form suspension; 8 to 12 percent of the culture suspension solution is respectively inoculated into the breeding culture solution of flatsour bacterium or the agar culture solution of thermophilic acid-fast bacillus and tryptic soytone broth or BCP modified culture solution, cultivated in 35 to 37 DEG C for about 24 to 48 hours, then the culture solution of being same to that of pre-breeding is isolated and cultivated; by a series of biochemical test, spore bacteria and Staphylococci is identified to mainly exist in the tomato paste and as the main spoilage microorganism. The invention takes very important role in promoting the rapid development of tomato paste industry and keeping the dominant position of the tomato paste trade in international market.

Novel oxazolidinone derivatives with a difluorophenyl moiety, represented by Chemical Formula 1, pharmaceutically acceptable salts thereof, a preparation method thereof, and a pharmaceutical composition containing the same as an active ingredient are provided. Exhibiting potent inhibitory activity against Gram-positive bacteria including Haemophilus influenza and Coagulase negative staphylococci and resistant bacteria including vancomycin-resistant enterococci (VRE), the pharmaceutical composition is useful as an antibiotic.

The invention discloses a disinfection method of a goose shed. The method includes the steps: a, cleaning the goose shed and clearing goose dung; b, uniformly locating braziers and firing the braziers; c, putting appropriate Chinese mugwort leaves in the braziers above the charcoal fire; d, after disinfection and cooling, carrying out the braziers. The Chinese mugwort leaves need to be dried in the sun after harvesting; the Chinese mugwort leaves put in the braziers should keep in producing a lot of smoke, but without producing naked flame; the Chinese mugwort leaves can be added into the braziers for multiple times to enable fumigation to last for 30-90 minutes. By the disinfection method of the goose shed, various germs can be effectively inhibited from spreading in air, typhoid bacteria, mycobacterium tuberculosis, staphylococcus and the like in air can be killed, inhibiting effect on many kinds of pathogenic bacteria, funguses and viruses leading to different kinds of infectious and epidemic diseases is achieved, and plague is prevented.

Antibodies to the CNA protein and to other regions from the collagen binding domain, including domain CNA19, are provided, and antibodies produced in this manner have been shown to be cross reactive to both Staphylococcus aureus and Staphylococcus epidermidis bacteria and which can thus be used in the prevention and treatment of infections caused by both of these types of bacteria. In addition, medical instruments can be treated using the antibodies of the invention in order to reduce or eliminate the possibility of their becoming infected or further spreading the infection. In particular, the proteins are advantageous because they are cross-reactive and may thus be administered to patients so as to reduce or prevent severe infection by staphylococcal bacteria of more than one species. Antibodies generated in this manner have also been shown to exhibit displacement activity and can thus be utilized advantageously in methods wherein these antibodies will be administered to patients having pre-existing staphylococcal infections because of the ability to displace bacterial proteins from binding sites on the extracellular matrix. Finally, a method of identifying, isolating and utilizing displacing antibodies is also provided.

The invention discloses vulva lotion, which is prepared from the following components in parts by weight: 7 to 12 parts of Ecdysanthera rosea Hook. et Arn, 6 to 9 parts of spike of fungus-infected rice, 10 to 14 parts of ramose scouring rush herb, 12 to 16 parts of lobelia sessilifolia, 4.5 to 8.5 parts of mile swertia herb, 5 to 9 parts of radix cynanchi atrati, 5 to 10 parts of callicarpa longissima (hemsl.)merr., 8.5 to 13.5 parts of beautiful sweetgum fruit, 6 to 11 parts of Wusuli dragonflyorchis rhizome, 10 to 13 parts of wild tobacco, 7 to 10 parts of snake bramble seed, 5 to 8 parts of rhaphidophora peepla, and 3 to 6 parts of Arundina graminifolia (D. Don) Hochr.. The vulva lotion has the excellent effects that the vulva lotion can effectively inhabit the generation of microbial strains such as escherichia coli, staphylococcus, candida albicans and the like, and can protect and promote the growth and reproduction of beneficial bacteria at the same time; the vulva lotion obtained by the invention is simple in preparation method, low in cost, short in course of treatment, remarkable in curative effect, and convenient for popularization and use.

The invention relates to the technical field of aquatic products, in particular to a processing method of an astroconger myriaster fermented preserved product. The processing method comprises the following steps: (1) killing and cleaning astroconger myriaster; (2) soaking the cleaned astroconger myriaster with an aqueous solution containing 10% of maltose, 5% of lemon and 3% of edible salt for 1-2h; (3) taking out and draining the astroconger myriaster, and inoculating lactic acid bacteria, staphylococcus, yeast and aspergillus oryzae in a ratio of 8:3:5:4:1, performing fermentation at 31-35DEG C for 5-10 h, and then performing fermentation at 20-25 DEG C for 10-13 days; (4) soaking the astroconger myriaster in a skipjack enzymatic hydrolysate for 10-13 min; (5) performing baking at 110-120 DEG C for 20-30 min to obtain the astroconger myriaster fermented preserved product. The preserved product prepared with the method has full fragrance, rich taste and high amino acid content, andpeople's choice of the astroconger myriaster is enriched.

The present invention relates to a method for the application and implantation of starter cultures in products of animal origin for curing same, which comprises:

• • a) introducing one or more starter cultures of Staphylococcus and yeasts in a whole muscle product of animal origin by means of sprinkling, tumbling and massaging;
  • b) subjecting said product after step a) to maturation treatment with heat and humidity to favor starter culture growth;
  • d1) freezing the product after step b), stopping the starter culture biological activity; and
  • d2) cutting or slicing the frozen product; and
  • d3) subjecting cutted or sliced product to a rapid drying process for between 30 and 120 minutes; and
  • e) packing the dried product of animal origin.