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METHOD FOR CULTIVATION OF CALLUS CULTURE OF COMMON WORMWOOD (ARTEMISIA VULGARIS L.)

机译:常见艾草(ART蒿)的愈伤组织培养方法

摘要

FIELD: biotechnology.;SUBSTANCE: invention represents a method for producing callus culture of wild-common wormwood (Artemisia vulgaris L.) in in vitro conditions, including sterilization of wormwood seeds with hydrogen peroxide solutions (3 % solution) for 10 minutes, ethyl alcohol (70 % solution) for 1 minute, three times rinsing in sterile distilled water for 5 minutes, placing sterile seeds on a solid nutrient medium without hormones, the following composition, mg: NH4NO3 – 33000, KNO3 – 38000, CaCl2x2H2O – 8800, MgSO4x7H2O – 7400, KH2PO4 – 3400, KI – 166, H3BO3 – 1240, MnSO4x4H2O – 4460, ZnSO4x7H2O – 1720, Na2MoO4x2H2O – 50, CuSO4x5H2O – 5, CoCl2x6H2O – 5, FeSO4x7H2O – 5560, Na-EDTA – 7460, mesoinositol – 100, thiamine – 100, pyridoxine – 100, nicotinic acid – 100, saccharose – 2500, water – 1000 ml, agar – 7000, further placement of leaf explants obtained from seedlings into a nutrient medium of the following composition, mg: NH4NO3 – 33000, KNO3 – 38000, CaCl2x2H2O – 8800, MgSO4x7H2O – 7400, KH2PO4 – 3400, KI – 166, H3BO3 – 1240, MnSO4x4H2O – 4460, ZnSO4x7H2O – 1720, Na2MoO4x2H2O – 50, CuSO4x5H2O – 5, CoCl2x6H2O – 5, FeSO4x7H2O – 5560, Na-EDTA – 7460, mesoinositol – 100, casein hydrolyzate – 500, thiamine – 100, pyridoxine – 100, nicotinic acid – 100, saccharose – 30000, 2,4 dichlorophenoxyacetic acid – 1, 6-benzylaminopurine – 1, naphthylacetic acid – 1, water – 1000 ml, agar – 12000; wherein the cultivation of plants is carried out in the dark at temperature of 26±1 °C, humidity of room is 70±5 %, the subculturing cycle is 3 weeks.;EFFECT: invention allows to produce callus culture of common wormwood (Artemisia vulgaris L.) in in vitro conditions.;1 cl, 3 tbl
机译:技术领域:本发明代表了一种在体外条件下产生野生普通艾草(Artemisia vulgaris L.)的愈伤组织培养物的方法,包括用过氧化氢溶液(3%溶液)将艾草种子灭菌10分钟,用乙基酒精(70%溶液)1分钟,在无菌蒸馏水中漂洗3次,每次5分钟,将无菌种子放在不含激素的固体营养培养基上,其组成如下,mg:NH 4 NO 3 – 33000,KNO 3 – 38000,CaCl 2 x2H 2 O – 8800,MgSO 4 x7H 2 O – 7400,KH 2 PO 4 – 3400,KI – 166,H 3 BO 3 – 1240,MnSO 4 x4H 2 O – 4460,ZnSO 4 x7H 2 O – 1720,Na 2 MoO 4 x2H 2 O – 50,CuSO 4 x5H 2 O – 5,CoCl 2 x6H 2 O – 5,FeSO 4 x7H 2 O – 5560,钠-EDTA – 7460,中肌醇– 100,硫胺素– 100,吡ido醇– 100,烟酸– 100,蔗糖– 2500,水– 1000 ml,琼脂– 7000,将从幼苗获得的叶外植体进一步放入具有以下成分的营养培养基中,mg:NH 4 NO 3 – 33000,KNO 3 – 38000,CaCl 2 x2H 2 O – 8800,MgSO < Sub> 4 x7H 2 O – 7400,KH 2 PO 4 – 3400,KI – 166,H 3 BO 3 – 1240,MnSO 4 x4H 2 O – 4460,ZnSO 4 x7H 2 O – 1720,Na 2 MoO 4 x2H 2 O – 50,CuSO 4 x5H 2 O – 5,CoCl 2 x6H 2 O – 5,FeSO 4 x7H 2 < / Sub> O – 5560,Na-EDTA – 7460,中肌醇– 100,酪蛋白水解物– 500,硫胺素– 100,吡ido醇– 100,烟酸– 100,蔗糖– 30000,2,4二氯苯氧乙酸– 1,6-苄基氨基嘌呤– 1,萘乙酸– 1,水– 1000毫升,琼脂– 12000;其中植物的培养是在黑暗中于26±1°C的温度,室内湿度为70±5%的条件下进行的,继代培养周期为3周。;效果:本发明可以产生普通艾草的愈伤组织培养物(蒿寻常条件下); 1 cl,3 tbl

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