주정을 이용한 염장발효식품의 탈염방법
    2.
    发明公开
    주정을 이용한 염장발효식품의 탈염방법 有权
    盐水和发酵食品的脱盐方法

    公开(公告)号:KR1020110047291A

    公开(公告)日:2011-05-09

    申请号:KR1020090103863

    申请日:2009-10-30

    CPC classification number: A23L5/23

    Abstract: PURPOSE: A desalting method of salted and fermented food using alcohol is provided to economically desalting the food using a food additive, a food storage tank, and an evaporation-condensing system. CONSTITUTION: A desalting method of salted and fermented food using alcohol comprises the following steps: inserting alcohol or 95% ethanol into the salted and fermented food, and settling for 1~36hours at 15~25deg C for inducing the salt precipitation; physically removing the salt from the food; and removing the alcohol or the ethanol from the food using a low temperature vacuum evaporation method at 10~50deg C. The amount of the alcohol or the ethanol is 1~5times greater than the amount of the salted and fermented food.

    Abstract translation: 目的:提供使用酒精的盐渍和发酵食品的脱盐方法,以使用食品添加剂,食品储存罐和蒸发冷凝系统对食品进行经济脱盐。 构成:使用酒精的咸咸发酵食品的脱盐方法包括以下步骤:将酒精或95%乙醇加入盐渍发酵食品中,并在15〜25℃下沉降1〜36小时,诱导盐析; 从食物中物理清除盐; 并使用低温真空蒸发法在10〜50℃下从食物中除去醇或乙醇。酒精或乙醇的量比盐渍发酵食品的量大1〜5倍。

    멍게 물렁증 기생충의 유전자 및 멍게 물렁증 진단 방법
    4.
    发明公开
    멍게 물렁증 기생충의 유전자 및 멍게 물렁증 진단 방법 有权
    天竺葵引起死亡的基因及其诊断方法

    公开(公告)号:KR1020070085012A

    公开(公告)日:2007-08-27

    申请号:KR1020060098722

    申请日:2006-10-11

    CPC classification number: C12Q1/6893 A01K67/0336 C12Q2600/158

    Abstract: A gene of a parasite causing death of Halocynthia roretzi and a method for diagnosing a parasite are provided to obtain a living organism that causes perishing of Halocynthia roretzi, and to diagnose a parasite by using a part of 18S rDNA fraction causing perishing of Halocynthia roretzi. A method for diagnosing a parasite includes the steps of: separating the entire nucleic acid from Halocynthia roretzi; performing PCR reaction by having the separated nucleic acid as a template and having a front primer and a reverse primer having a partial sequence of 18SrDNA fraction having a nucleotide sequence of sequence number 1 as a primer pair; and checking the size of the product of the PCR reaction by gel electrophoresis and comparing the size of the aforesaids product with the size of the product that is anticipated from the used primer pair.

    Abstract translation: 提供了引起Halocynthia roretzi死亡的寄生虫的基因和用于诊断寄生虫的方法,以获得导致Halocynthia roretzi死亡的生物体,并且通过使用引起Halocynthia roretzi灭活的18S rDNA部分的一部分来诊断寄生虫。 用于诊断寄生虫的方法包括以下步骤:将全部核酸与Halocynthia roretzi分离; 通过使分离的核酸作为模板并具有前序引物和具有序列号为1的核苷酸序列的部分序列的18SrDNA部分的反向引物作为引物对进行PCR反应; 并通过凝胶电泳检查PCR反应产物的大小,并将无菌产物的大小与从使用的引物对预期的产物的大小进行比较。

    불가사리로부터 콜라겐을 제조하는 방법
    5.
    发明公开
    불가사리로부터 콜라겐을 제조하는 방법 有权
    从STARFISH制备胶原蛋白的方法

    公开(公告)号:KR1020060125995A

    公开(公告)日:2006-12-07

    申请号:KR1020050047528

    申请日:2005-06-03

    CPC classification number: C07K1/12 C07K1/34 C07K1/36 C07K14/43504

    Abstract: A method for preparing atelocollagen from starfish is provided to mass-produce the atelocollagen without lowering yield by removing non-collagen materials using alkaline materials and adjusting pH of a solution into acidic value. And a method for preparing collagen peptide from starfish using the same is provided to produce collagen peptide from the atelocollagen using a neutral protease without degeneration of the collagen. The method for preparing atelocollagen from starfish comprises the steps of: (a) removing non-collagen materials existing in a starfish body wall using an alkali material selected from the group consisting of NaOH, Ca(OH)2, and Na2CO3 to prepare insoluble collagen fiber; and (b) after adjusting pH using tartaric acid or citric acid into the acidic state, preparing atelocollagen from the collagen fiber using an acidic protease such as 1% pepsin at a temperature of 5-10 deg.C. To prepare collagen peptide from the starfish, the atelocollagen prepared from the above method is hydrolyzed with a neutral protease.

    Abstract translation: 提供了从海星制备无胶原的方法,通过使用碱性物质除去非胶原物质并将溶液的pH调节为酸性值,大量生产无胶原体而不降低产率。 提供了使用其从海星制备胶原肽的方法,以使用不含胶原变性的中性蛋白酶从成骨胶原产生胶原肽。 从海星制备骨胶原的方法包括以下步骤:(a)使用选自NaOH,Ca(OH)2和Na 2 CO 3的碱性物质除去存在于海星体壁中的非胶原材料,以制备不溶性胶原 纤维; 和(b)在使用酒石酸或柠檬酸调节pH至酸性状态后,使用酸性蛋白酶如1%胃蛋白酶在5-10℃的温度下从胶原纤维中制备胶原蛋白。 为了从海星制备胶原肽,由上述方法制备的胶原蛋白用中性蛋白酶水解。

    불가사리를 이용한 칼슘보충제의 제조방법
    6.
    发明公开
    불가사리를 이용한 칼슘보충제의 제조방법 有权
    使用STARFISHES生产钙补充剂的方法

    公开(公告)号:KR1020010085034A

    公开(公告)日:2001-09-07

    申请号:KR1020010044347

    申请日:2001-07-24

    Abstract: PURPOSE: A method for producing calcium supplementary agents using starfishes is provided, therefore, the starfish, which is harmful to sea farm, can be effectively used and it amount can be decreased. CONSTITUTION: The method for producing calcium supplementary agents using starfishes comprises the steps of: extracting and removing saponin harmful to human from starfishes using alcohol or ethanol; removing shellfish toxin and tetrodo toxin from starfishes by dipping the starfishes in vinegar or acetic acid; hydrolyzing the starfishes in a shaking water tank having constant temperature using protease; and crushing the precipitated cartilage of starfishes, followed by filtering and freeze-drying the crashed cartilage of starfishes.

    Abstract translation: 目的:提供使用星形鱼类生产钙补充剂的方法,因此可有效利用对海域有害的海星,降低量。 构成:使用星形鱼制备钙补充剂的方法包括以下步骤:使用酒精或乙醇从星形藻中提取和去除对人有害的皂素; 通过将星形鱼浸入醋或醋酸中,从星体鱼中去除贝类毒素和四唑毒素; 使用蛋白酶水解具有恒定温度的摇动水箱中的星形鱼; 并粉碎沉淀的星形软骨,然后过滤并冷冻干燥坠落的星体软骨。

    추출용매에 의한 크릴의 불소 저감 방법
    8.
    发明授权
    추출용매에 의한 크릴의 불소 저감 방법 有权
    通过萃取溶剂在KRILL中减少氟化物的方法

    公开(公告)号:KR101174474B1

    公开(公告)日:2012-08-22

    申请号:KR1020110098249

    申请日:2011-09-28

    CPC classification number: A23L5/23 A23L17/40

    Abstract: PURPOSE: A fluorine reduction method of krill using an extraction solvent is provided to remove or reduce fluorine from the collected krill during before processing or packaging using organic acid, inorganic acid, or an alkali solution. CONSTITUTION: A fluorine reduction method of krill using an extraction solvent comprises a step of adding 10-200 times the amount of fluorine extraction solvent by the weight of the krill to the collected krill for soaking and stirring the mixture for 2-60 minutes. The fluorine extraction solvent is one or more than two compound selected from organic acid, inorganic acid, and an alkali solution. The organic acid includes citric acid, tartaric acid, lactic acid, oxalic acid, succinic acid, malic acid, and formic acid. The inorganic acid includes hydrochloric acid, sulfuric acid, nitric acid, perchloric acid, boric acid, and phosphoric acid. The alkali solution includes sodium hydroxide, calcium hydroxide, an ammonia solution, sodium carbonate, potassium carbonate, magnesium carbonate, ammonium carbonate, ammonium chloride, urea, and ammonia salt.

    Abstract translation: 目的:提供使用提取溶剂的磷虾的氟还原方法,以在使用有机酸,无机酸或碱溶液处理或包装之前,从收集的磷虾中除去或减少氟。 构成:使用提取溶剂的磷虾的氟还原法包括将10-2倍量的氟提取溶剂以磷虾的重量加入到收集的磷虾中,浸泡和搅拌混合物2-60分钟。 氟提取溶剂是选自有机酸,无机酸和碱溶液中的一种或两种以上的化合物。 有机酸包括柠檬酸,酒石酸,乳酸,草酸,琥珀酸,苹果酸和甲酸。 无机酸包括盐酸,硫酸,硝酸,高氯酸,硼酸和磷酸。 碱溶液包括氢氧化钠,氢氧化钙,氨溶液,碳酸钠,碳酸钾,碳酸镁,碳酸铵,氯化铵,尿素和氨盐。

    매생이 열수추출물을 함유하는 면역 활성 증가용 조성물
    10.
    发明授权
    매생이 열수추출물을 함유하는 면역 활성 증가용 조성물 有权
    用于增加包含来自加利福尼亚州的热水提取物的免疫活性的组合物

    公开(公告)号:KR100857249B1

    公开(公告)日:2008-09-08

    申请号:KR1020070030681

    申请日:2007-03-29

    Abstract: A composition comprising the extract of Capsosiphon fulvescens is provided to increase immune activity of complement system in human body by promoting production of IgA(immunoglobulin A) antibody, and inhibit growth of cancer cells without side effects and toxicity to human, so that the composition is useful to treat and prevent various diseases. A composition for increasing immune activity comprises the extract of Capsosiphon fulvescens with molecular weight of 300-500kDa which is prepared by extracting Capsosiphon fulvescens in hot water at 90-110 deg. C for 2-4 hours, precipitating the hot water extract of Capsosiphon fulvescens with alcohol, and ultrafiltering the precipitates, wherein the daily dosage of the composition is 1-1000 mg/kg.

    Abstract translation: 提供了含有辣椒皂苷提取物的组合物,通过促进IgA(免疫球蛋白A)抗体的产生,抑制癌细胞的生长而不会对人体产生副作用和毒性,从而增加人体补体系统的免疫活性, 有用于治疗和预防各种疾病。 用于增加免疫活性的组合物包括分子量为300-500kDa的辣椒皂苷提取物,其通过在90-110℃的热水中提取辣椒皂苷来制备。 C 2-4小时,用酒精沉淀辣椒粉的热水提取物,超滤沉淀物,其中组合物的日剂量为1-1000mg / kg。

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