Abstract:
PURPOSE: An osmotic stress resistant yeast transformed by a recombinant vector containing the GPD gene that isolated from Pleurotus sajor-caju is provided for improving the osmotic stress resistance of yeast. CONSTITUTION: The osmotic stress resistant yeast transformed by a recombinant vector containing glycerol-3-phosphate dehydrogenase(GPD) gene as an osmotic stress related gene is obtained by the following steps of: incubating Pleurotus sajor-caju ASI 2070 in an MCM medium containing 20g of peptone, 2g of yeast extract, 2g of K2HPO4, 1.0g of KH2PO4, 0.46g of MgSO47H2O, 0.5g of DW1L at 25 deg. C for 15 days; filtering with mira cloth; separating total RNA and DNA of Pleurotus sajor-caju ASI 2070 by using a Graham method and a Sambrook method, respectively; preparing the pYES2 vector containing the GPD gene by using restriction enzymes; and transforming Saccharomyces cerevisiae INVSC2 with the pYES2 vector.
Abstract translation:目的:提供通过含有从侧耳属sajor-caju分离的GPD基因的重组载体转化的渗透胁迫酵母,用于改善酵母的渗透胁迫性。 构成:通过含有甘油-3-磷酸脱氢酶(GPD)基因的重组载体转化的渗透压胁迫酵母作为渗透胁迫相关基因,通过以下步骤获得:将Pleurotus sajor-caju ASI 2070在含有20g的MCM培养基中培养 的蛋白胨,2g酵母提取物,2g K 2 HPO 4,1.0g KH 2 PO 4,0.46g MgSO 4·7H 2 O,0.5g DW1L,25℃。 C 15天; 用米拉布过滤; 分别使用Graham方法和Sambrook方法分离了侧耳菇sajor-caju ASI 2070的总RNA和DNA; 通过使用限制酶制备含有GPD基因的pYES2载体; 并用pYES2载体转化酿酒酵母INVSC2。
Abstract:
본 발명은 벼 유래의 OsZIP1 단백질 및 이를 코딩하는 핵산 분자에 관한 것이다. 본 발명의 OsZIP1 핵산 분자를 이용하여 식물체를 형질전환시킴으로써, 병 저항성을 가지며, 야생형에 비하여 식물 개체의 크기 감소, 수술 길이의 단축, 꽃의 크기 축소 또는 화분 미형성의 생육 억제 양상 및 진한 화색의 표현형을 유도할 수 있으며, 이를 통해 식물(특히, 화훼작물)의 생산성 및 상품성(미니 꽃 생산)의 증대를 도모할 수 있다. 병 저항성, 벼, 담배, OsZIP1, 생육 억제
Abstract:
PURPOSE: An StMyb gene having salt-resistance or drought-resistance of plant is provided to use in developing plant species. CONSTITUTION: An StMyb(Solanum tuberosum Myb) polypeptide comprises an amino acid of sequence number 1. An StMyb polynucleotide has a gene sequence of sequence number 2. The intracellular increase of StMyb polypeptide is performed by transforming a plant with a vector containing the polynucleotide and a promoter. A method for producing the plant enhancing salt tolerance or drought tolerance comprises: a step of overexpressing StMyb polypeptide having amino acid of sequence number 1; and a step of transforming the plant with the expression vector.
Abstract:
A method for control of gray mold caused by Botrytis cinerea is provided to inhibit growth of Botrytis cinerea without specific equipments and technique by treating a plant with a single frequency sound, so that the gray mold is suppressed in an environment-friendly manner. The gray mold caused by Botrytis cinerea is controlled by treating a subject plant with a single frequency sound selected from 250-500 Hz generated by a sound generator, wherein the plant is vegetable including tomato, cucumber, strawberry, lettuce, eggplant and red pepper, or flower including lily, gladiolus, rose and carnation.
Abstract:
PURPOSE: A wound stress-induced promoter is provided to enhance the harvest amount of various crops and to produce commercial crops without environmental harm. CONSTITUTION: A wound stress-induced promoter derived from Oryza sativa has a base sequence of sequence number 1. The promoter contains a recombinant plant expression vector. The recombinant plant expression vector is prepared by operatively linking a target gene encoding a target protein at downstream of the promoter. The target protein is a plant disease resistant protein, a high functional protein, a cell regulatory protein, an immunomodulatory protein, an inhibitory protein, or an enzyme. A method for producing a transgenic plant comprises: a step of transforming plant cells with the recombinant plant expression vector; and a step of redifferentiating the transgenic plant.
Abstract:
PURPOSE: A broad host range disease resistance gene OsRBI1 is provided to promote expression of genes the enhance plant disease-resistance. CONSTITUTION: A plant has enhanced disease-resistance by improving intracellular level of polypeptide with an amino acid sequence of the sequence number 1. A method for producing a plant with enhanced disease-resistance comprises: a step of preparing an expression vector which overexpresses a polypeptide with the amino acid of the sequence number 1; and a step of transforming the plant with the expression vector. The expression vector comprises a promoter and a polynucleotide which is operably linked to the promoter and encodes the polypeptide of the sequence number 1.