Abstract:
PURPOSE: A beta-carotene hydroxylase 1 gene promoter and expression vector having the same are provided to induce expression of target protein through whole plant body. CONSTITUTION: An AtBch1 promoter for inducing constitutive expression comprises a nucleotide sequence of sequence number 1. A recombinant vector for inducing constitutive expression contains the promoter. The vector is pBGWFS7-PAtBch1 vector(KACC 95096P). A transgenic plant is prepared using transformed cells and the vector.
Abstract:
본 발명은 식물체 내에 외래 유용유전자의 발현 장소를 뿌리 부분으로 제한하여 발현시키는 뿌리 특이 발현 프로모터에 관한 것으로서, 더욱 상세하게는 서열번호:1로 구성되는 뿌리 특이 발현 프로모터, 서열번호:2로 구성되는 올리고 누클레오티드 및 서열번호:3으로 구성되는 올리고누클레오티드로 이루어지는 상기 뿌리 특이 프로모터를 증폭하기 위한 프라이머, 상기 서열번호:1의 프로모터 서열을 포함하는 것을 특징으로 하는 발현벡터 pBGWFS7-PAtRA166 및 상기 발현벡터 pBGWFS7-PAtRA166 으로 형질전환된 식물세포에 관한 것이다. 뿌리특이, 프로모터, 애기장대, 조직특이, 형질전환체
Abstract:
PURPOSE: A microsatellite marker for distinguishing lineage of red mold pathogen and a method for distinguishing lineage of red mold pathogen using the same are provided to quickly and accurately distinguish lineage of a main contamination source of complex red mold pathogen from a grain sample by analyzing PCR using FgmsAAG93. CONSTITUTION: A primer, FgmsAAG93, of sequence numbers 1 and 2 is used for specifically amplifying a microsatellite of red mold to distinguish lineage of a main contamination source among red mold pathogens. A method for distinguishing lineage of F. graminearum comprises: a step of amplifying a gene using FgmsAAG93; and a step of identifying a microsatellite site of the amplified gene. A kit for distinguishing and diagnosing lineage of the red mold pathogens contains the primer and a reagent for amplification.
Abstract:
PURPOSE: A primer pair for detecting deoxynivalenol(DON)-producing Gibberella zeae and a kit using the same are provided to quickly and accurately diagnose DON. CONSTITUTION: A primer pair for detecting DON-producing Gibberella zeae is denoted by sequence numbers 1 and 2. The Gibberella zeae is Fusarium graminearum. A kit for detecting the Gibberella zeae contains the primer pair. A method for detecting the Gibberella zeae using the primer pair comprises: a step of isolating RNA from a sample of Oryza sativa, barley, and wheat; a step of amplifying a target sequence by RT-PCR; and a step of detecting a PCR product.
Abstract:
PURPOSE: A novel plant constitutive promoter is provided to express a foreign gene regardless of expression place and to develop transgenic plant. CONSTITUTION: A plant constitutive promoter contains partial or whole base of sequence number 1. The constitutive promoter is derived from Arabidopsis thaliana. A plant constitutive promoter, Lip2 is obtained by performing PCR of oligonucleotide of sequence numbers 6 and 7. A recombinant expression vector pBGWFS7-PAtLip3(deposit number: KACC 95086P) contains the plant constitutive promoter. The plant expression vector which is able to express a target gene is prepared using the constitutive promoter.
Abstract:
본 발명은 식물체 내에 외래 유용유전자의 발현 장소를 뿌리 부분으로 제한하여 발현시키는 뿌리 특이 발현 프로모터에 관한 것으로서, 더욱 상세하게는 서열번호:1로 구성되는 뿌리 특이 발현 프로모터, 서열번호:2로 구성되는 올리고 누클레오티드 및 서열번호:3으로 구성되는 올리고누클레오티드로 이루어지는 상기 뿌리 특이 프로모터를 증폭하기 위한 프라이머, 상기 서열번호:1의 프로모터 서열을 포함하는 것을 특징으로 하는 발현벡터 pBGWFS7-PAtM19PK 및 상기 발현벡터 pBGWFS7-PAtM19PK으로 형질전환된 식물세포에 관한 것이다. 뿌리특이, 프로모터, 애기장대, 조직특이, 형질전환체
Abstract:
A method for enhancing the resistance against plant diseases and a transformant over-expressing an OsWRKY6 gene are provided to be utilized as a molecular breeding material for developing a disease-resistant crop by having excellent bacterial blight resistance in rice as well as resistance against wide range of pathogenic bacteria range resistance, be used for various crops because other crops preserve well disease defense mechanism relating to the OsWRKY6 gene and decrease the use of pesticide due to the disease resistant species breeding, thereby improving the productivity and supplying safe agricultural products. A method for enhancing the resistance against plant diseases comprises the steps of: (a) preparing an expression vector pB2GW7-OsWRKY6 having a cleavage map depicted in Fig. 4b including an OsWRKY6 gene consisting of SEQ ID : NO. 1; and (b) introducing the expression vector into a plant cell to prepare a transformant over-expressing the OsWRKY6 gene. A transformant is transformed by the expression vector pB2GW7-OsWRKY6, wherein the transformant is selected from the group consisting of a rice cell, a cabbage cell, a hot pepper cell, a potato cell and a rape cell. Further, the plant diseases are selected from a group consisting of Bacterial blight, rice blast disease, Rice stripe tenuivirus, Rhizoctonia solani, Rice Black-Streaked Dwarf Virus and Mycosphaerella leaf spot.