초록장님노린재 유인용 성페로몬 조성물 및 이의 용도

    公开(公告)号:KR101726598B1

    公开(公告)日:2017-04-18

    申请号:KR1020140154342

    申请日:2014-11-07

    Abstract: 본발명은헥실부티레이트(hexyl butyrate), (E)-2-헥세닐부티레이트((E)-2-hexenyl butyrate), (E)-4-옥소-2-헥세날((E)-4-oxo-2-hexenal) 및 (E)-2-옥테닐부티레이트((E)-2-octenyl butyrate)를포함하는초록장님노린재유인용성페로몬조성물및 이를이용한교미교란제또는페로몬트랩에관한것이다. 본발명에따르면초록장님노린재에대한유인효과가높은초록장님노린재유인용페로몬조성물을제공할수 있고, 이를이용한교미교란제또는페로몬트랩을통하여과수피해를경감시키고과수원에살충제사용량을획기적으로줄일수 있다.

    해충에 높은 병원성이 있어 선발된 신규한 메타리지움아니소플리애 곰팡이 및 이를 이용한 미생물살충제 조성물
    15.
    发明公开
    해충에 높은 병원성이 있어 선발된 신규한 메타리지움아니소플리애 곰팡이 및 이를 이용한 미생물살충제 조성물 无效
    使用相同方法的金属盐异味和微生物杀虫剂组合物的新型微生物

    公开(公告)号:KR1020080006679A

    公开(公告)日:2008-01-17

    申请号:KR1020060065686

    申请日:2006-07-13

    CPC classification number: A01N63/04 A01N25/04 A01N25/08 C12N1/14 C12R1/645

    Abstract: A Metarhizium anisopliae NIAST-IPL012 is provided to contribute the industrialization of M. anisopliae by maximizing the recovery rate of spores and be adequately used as a microorganism insecticide composition by improving the stability during storage and distribution of the spores, thereby accelerating the domestic microorganism pesticide industry and continuing the environmental-friendly agriculture. A Metarhizium anisopliae NIAST-IPL012 is deposited as a deposition no. KFCC-11362P. A method for culturing the Metarhizium anisopliae NIAST-IPL012 comprises the steps of: (a) inoculating the Metarhizium anisopliae NIAST-IPL012 into cooked rice or rice seed culture medium at a temperature of 26-28 deg.C one time per one to two days interval; and (b) culturing it for 12-14 days. A microbial insecticide composition comprises the Metarhizium anisopliae NIAST-IPL012 as an effective ingredient and further comprises at least one additive selected from the group consisting of a dispersing agent, a moisturizing agent, a UV blocking agent and an emulsifying agent.

    Abstract translation: 提供了一种Metarhizium anisopliae NIAST-IPL012,通过最大限度地提高孢子的回收率,有效地促进了五角茴香的工业化,并通过提高孢子储存和分配过程中的稳定性,充分利用了微生物杀虫剂组合物,从而加速了国内微生物农药 产业化,继续开展环保型农业。 将Metasthizium anisopliae NIAST-IPL012沉积为沉积物。 KFCC-11362P。 用于培养Metarhizium anisopliae NIAST-IPL012的方法包括以下步骤:(a)在26-28℃的温度下将米色氏甲酸杆菌NIAST-IPL012接种到熟米或稻种子培养基中,每1至2天一次 间隔; 和(b)培养12-14天。 微生物杀虫剂组合物包含作为有效成分的金属异青霉NIAST-IPL012,还包含选自分散剂,保湿剂,UV阻断剂和乳化剂中的至少一种添加剂。

    초록장님노린재 유인용 성페로몬 조성물 및 이의 용도
    18.
    发明公开
    초록장님노린재 유인용 성페로몬 조성물 및 이의 용도 有权
    用于吸收白萝卜(MEERER-DUR)的SEX PHEROMONE组合物及其用途

    公开(公告)号:KR1020160054831A

    公开(公告)日:2016-05-17

    申请号:KR1020140154342

    申请日:2014-11-07

    CPC classification number: A01N31/02 A01N35/02 A01N37/44 Y10S514/919

    Abstract: 본발명은헥실부티레이트(hexyl butyrate), (E)-2-헥세닐부티레이트((E)-2-hexenyl butyrate), (E)-4-옥소-2-헥세날((E)-4-oxo-2-hexenal) 및 (E)-2-옥테닐부티레이트((E)-2-octenyl butyrate)를포함하는초록장님노린재유인용성페로몬조성물및 이를이용한교미교란제또는페로몬트랩에관한것이다. 본발명에따르면초록장님노린재에대한유인효과가높은초록장님노린재유인용페로몬조성물을제공할수 있고, 이를이용한교미교란제또는페로몬트랩을통하여과수피해를경감시키고과수원에살충제사용량을획기적으로줄일수 있다.

    Abstract translation: 本发明涉及一种用于诱导三叶草的性信息素组合物和一种交配扰乱物或使用其的信息素捕获物,其中用于诱导羊茅的性信息素组合物包括丁酸己酯,(E)-2-己烯基丁酸酯,(E) -4-氧代-2-己烯醛和(E)-2-辛烯基丁酸酯。 根据本发明,提供了一种诱导枸杞的性信息素组合物,其对诱导枸杞子具有高效果。 通过使用其的交配扰乱物或信息素捕获物,会降低果实的损害,果园中杀虫剂的使用量可能显着降低。

    토마토반점위조바이러스 저항성 판별 방법
    20.
    发明公开
    토마토반점위조바이러스 저항성 판별 방법 有权
    确定对番茄斑点枯萎病毒抗性的方法

    公开(公告)号:KR1020120121639A

    公开(公告)日:2012-11-06

    申请号:KR1020110039560

    申请日:2011-04-27

    CPC classification number: C12Q1/701 C12Q2600/13

    Abstract: PURPOSE: A method for determining tomato spotted wilt virus resistance using tomato spotted wilt virus is provided to evaluate resistance of improved Capsicum annuum and tomato species. CONSTITUTION: A method for determining tomato spotted wilt virus resistance in Capsicum annuum species comprises: a step of isolating RNA from a target Capsicum annuum species and preparing cDNA; a step of performing PCR using a PCR primer set corresponding to DNA encoding one nucleocapsid protein among sequence numbers 1-5; and a step of determining the presence of sequences corresponding to the sequence numbers 1-5.

    Abstract translation: 目的:提供一种利用番茄斑点枯萎病毒测定番茄斑点枯萎病毒抗性的方法,以评估改良辣椒和番茄种类的抗性。 构成:在辣椒种中测定番茄斑点枯萎病毒抗性的方法包括:从目标辣椒种分离RNA并制备cDNA的步骤; 使用与编码序列号1-5中的一个核衣壳蛋白的DNA对应的PCR引物组进行PCR的步骤; 以及确定对应于序列号1-5的序列的存在的步骤。

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