Abstract:
PURPOSE: Fermented ganoderma lucidum and ginseng drink, and a producing method thereof are provided to enable users to intake active ingredients of ginseng regardless of the physical constitution. CONSTITUTION: A producing method of fermented ganoderma lucidum and ginseng drink comprises the following steps: washing fresh ginseng, and naturally drying the ginseng for 3-5 hours; slicing the dried ginseng, and inserting the ginseng slices into cultivation bottles 100-150g for each bottle; sterilizing the ginseng for 60 minutes at 121 deg C using an autoclave; injecting 5-30% of ganoderma lucidum spawns to the sterilized ginseng, and solid-fermenting the mixture for 30-50 days at 25-30 deg C; vacuum-freezing and drying the fermented ganoderma lucidum and ginseng; adding additional ingredients into the fermented ganoderma lucidum and ginseng, and extracting the mixture for 8-24 hours at 100deg C before filtering: and adding 4-10% of liquid fructose, 4-10% of fructo-oligosaccharide, 1-5% of multiflora honey, 0.2-1% of taurine, 0.2-1% of polydextrose, 1-3% of dextrin, and 0.1-0.5% of pectin into 50-80% of fermented ganoderma lucidum and ginseng extract.
Abstract:
PURPOSE: An immunity activating composition containing polysaccharide separated from a phellinus linteus mycelial fermentation product of ginseng is provided to activate immune cells forming the internal immune system of a user for preventing the infection from viruses or bacteria. CONSTITUTION: An immunity activating composition contains polysaccharide separated from a phellinus linteus mycelial fermentation product of ginseng. The ginseng is selected from the group consisting of fresh ginseng, red ginseng, woods grown ginseng, and wild ginseng. The phellinus linteus mycelial fermentation product of the ginseng is a fraction separated from a hot water extract of a fermentation product obtained by cultivating the ginseng using a phellinus linteus mycelium. The composition has a form selected from a tablet, a hard or soft capsule, a liquid agent, or a suspension agent.
Abstract:
PURPOSE: A method of culturing mushroom is provided to culture mushrooms containing beneficial components of Hippophae rhamnoides by cultivating the mushrooms in a culture medium containing powder of the Hippophae rhamnoides. CONSTITUTION: A mycelium is obtained by inoculating spawns of lion`s mane mushrooms into a plating medium, and cultivating for 13 to 17 days at the culture temperature of 23 deg. C to 26 deg. C(S110). Multiple mycelium discs are manufactured by cutting the mycelium(S120). The first inoculum source is obtained by inoculating a mycelium disc into a MCM medium and shake-cultivating for 7-12 days at the culture temperature of 23deg. C to 26deg. C(S130). The second inoculum source is obtained by inoculating the first inoculum source into the MCM medium and shake cultivating for 5-7 days at the culture temperature of 23deg. C to 26deg. C(S140). After inoculating the second inoculum source into the MCM medium containing powder of Hippophae rhamnoides, the MCM medium is shake cultivated for 8-10 days at the culture temperature of 23deg. C to 26deg. C(S150). The volume of the first inoculum source to be inoculated into the MCM medium in the stage of obtaining the second inoculum source is 10 vol% to 15 vol% of the total volume of the first inoculum source obtained in the stage of obtaining the first inoculum source. The volume of the second inoculum source to be inoculated into MCM medium in the stage of shake cultivation of the second inoculum source is 10 vol% to 15 vol% of the total volume of the second inoculum source obtained in the stage of obtaining the second inoculum source. [Reference numerals] (AA) Start; (BB) End; (S110) Inoculating spawns of lion`s mane mushrooms into a plating medium, and cultivating for 13-17 days at 23-26 deg. C; (S120) Manufacturing multiple mycelium discs by cutting the mycelium; (S130) Obtaining a first inoculum source by inoculating the mycelium discs in an MCM medium and shake-cultivating for 7-12 days at 23-26 deg. C; (S140) Obtaining a second inoculum source by inoculating the first inoculum source in the MCM medium and shake-cultivating for 5-7 days at 23-26 deg. C; (S150) Inoculating the second inoculum source in an MCM medium containing Sea Buckthorn powder, and cultivating for 8-10 days at 23-26 deg, C
Abstract:
본 발명은 흑마늘과 상황균사체 분말을 이용한 생리활성 강화 보쌈용 김치에 관한 것이다. 본 발명에 따른 생리활성 강화 보쌈용 김치는 절임무채 13~17중량%, 고춧가루 4.5~5.5중량%, 백설탕 2.4~2.5중량%, 흑마늘 1.7~1.9중량%, 현미상황균사체 분말 1.8~2.2중량%, 배 1.4~1.6중량%, 미나리 1.4~1.6중량%, 염장새우 1.4~1.6중량%, 양파 1.4~1.6중량%, 생강 0.9~1.1중량%, 쪽파 0.6~0.8중량%, L-글루타민산나트륨 0.4~0.6중량%, 참기름 0.25~0.35중량%, 잣 0.08~0.12중량%, 참깨 0.08~0.12중량%, 5'-리보뉴클레오티드이나트륨 0.015~0.025중량% 및 잔량의 절임배추를 포함하는 것을 특징으로 한다. 김치, 흑마늘, 상황균사체
Abstract:
PURPOSE: Kimchi for bossam(boiled pork wrapped in greens) with the enhanced physiological activity is provided to improve the anti-oxidation property, the immunity, and the anticancer activity of the kimchi. CONSTITUTION: Kimchi for bossam(boiled pork wrapped in greens) with the enhanced physiological activity contains 13~17wt% of pickled white radish slices, 4.5~5.5wt% of red pepper powder, 2.4~2.5wt% of white sugar, 1.7~1.9wt% of black garlic, 1.8~2.2wt% of phellinus linteus mycelium powder using brown rice, 1.4~1.6wt% of pear, 1.4~1.6wt% of oenanthe javanica, 1.4~1.6wt% of salted shrimps, 1.4~1.6wt% of onions, 0.9~1.1wt% of ginger, 0.6~0.8wt% of leak, 0.4~0.6wt% of monosodium L-glutamate, 0.25~0.35wt% of sesame oil, 0.08~0.12wt% of pine corn, 0.08~0.12wt% of sesame, 0.015~0.025wt% of Disodium 5`-Ribonucleotide, and the balance of pickled Chinese cabbage.