Abstract:
본 발명은 재조합 대장균을 이용한 파필리오신의 대량 생산방법에 관한 것이다. 본 발명의 재조합 대장균을 이용한 파필리오신의 대량 생산방법은 호랑나비( Papilio
xuthus ) 유충 유래의 파필리오신 유전자를 갖는 형질전환된 재조합 대장균을 제조하는 단계와, 상기의 형질전환체인 재조합 대장균을 배양한 후, 이를 불용성 재조합 융합단백질로 발현한 후 분리 및 정제하여 파필리오신을 생산하는 단계를 포함하여 구성된다. 본 발명에 의해, 재조합된 파필리오신은 그람음성 세균 및 그람양성 세균 등의 각종 박테리아에 대하여 높은 항균활성을 나타내므로 천연 항생제로 유용하게 이용될 수 있다.
Abstract:
The present invention relates to a transgenic silkworm that produces red fluorescent silk. More specifically, a recombinant expression vector which includes a gene construct in which a marker gene regulatory promoter, a marker gene, a silkworm-derived fibroin promoter, and an anemone-derived red fluorescent gene are operatively linked and a silkworm is transformed by the recombinant expression vector so that a transgenic silkworm that produces red fluorescent silk can be produced. The red fluorescent silk that the transgenic silkworm produces represents thin natural red color even in natural light so that a separated coloring process is not needed and the silk is environment-friendly and economical. When a light beam of a particular wavelength is irradiated, the silk represents bright red fluorescent color in the darkness so as to be usefully used as material for high value clothes and fashion or wallpaper compared with general silk.
Abstract:
The present invention relates to a transgenic silkworm having hSCF recombinant protein. A method for preparing the transgenic silkworm having hSCF recombinant protein of the present invention comprises the steps of: introducing a dHsp70 promoter and a 3xP3 promoter to a transfer vector in order to prepare an expression vector for silkworm transformation; and micro-injecting the expression vector for the silkworm transformation into a silkworm egg and preparing a transduced transgenic silkworm. By the present invention, the transgenic silkworm, which is capable of mass producing stem cell factors (hSCF) which are useful to the human body at low costs, is provided. [Reference numerals] (1) Not transformed silkworm larva after 5 days;(2) Transformed silkworm larva after 5 days
Abstract:
PURPOSE: A papiliocin 2 gene isolated from a Papilio xuthus larva, an antipeptide using the same, and a method for producing a large amount of recombinant papiliocin 2 are provided to ensure antibacterial activity against gram-negative bacteria, Candida albicans, and resistant bacteria(MEREC). CONSTITUTION: A gene of antibacterial peptide papiliocin 2 is denoted by sequence number 7 and is isolated from Papilio xuthus larva. A recombinant antibacterial peptide papiliocin 2 is denoted by sequence number 9. A recombinant expression vector, pET32-Papiliocin2 contains the recombinant antibacterial peptide papiliocin 2. A recombinant E.col BL21(DE3)-(pET32-Papiliocin2) is formed by transforming with the recombinant expression vector pET32-Papiliocin2. A method for producing a large amount of the recombinant antibacterial peptide pailiocin 2 comprises: a step of preparing the recombinant antibacterial peptide papiliocin 2(sequence number 9); a step of preparing the recombinant E.coli by the recombinant expression vector containing the recombinant antibacterial peptide papiliocin 2; and a step of culturing the recombinant E.coli and isolating and purifying a water soluble recombinant fusion protein.
Abstract:
PURPOSE: A HSP70 promoter for transforming silkworm, a primer for amplifying the same, and an expression vector containing the promoter are provided to express green fluorescent genes in silkworm eggs and larvae, and to early determine transformation. CONSTITUTION: A HSP70 promoter for transforming silkworm is denoted by sequence number 1, and is isolated in a silkworm. A primer for amplifying the promoter has sequences of sequence numbers 2 and 3. An expression vector for transforming silkworm contains the HSP70 promoter. A method for preparing a silkworm transformant comprises: a step of treating a dormant silkworm egg with hydrochloric acid at 25 deg. C for 1 hour; a step of transducing green fluorescent gene at downstream of the HSP70 promoter(sequence number 1) and cloning fused vector to prepare the expression vector; and a step of microinjecting the expression vector to the silkworm egg.
Abstract translation:目的:提供用于转化蚕的HSP70启动子,其扩增引物和含有启动子的表达载体,以在蚕卵和幼虫中表达绿色荧光基因,并早期确定转化。 构成:用于转化蚕的HSP70启动子由序列号1表示,并在蚕中分离。 用于扩增启动子的引物具有序列号2和3的序列。转化蚕的表达载体含有HSP70启动子。 制备蚕转化体的方法包括:用25℃的盐酸处理休眠蚕卵的步骤。 C 1小时; 在HSP70启动子(序列号1)的下游转染绿色荧光基因并克隆融合载体以制备表达载体的步骤; 以及向蚕卵显微注射表达载体的步骤。
Abstract:
PURPOSE: A silkworm egg for transformation for producing green fluorescence silk and a transformant from the same are provided to stably and cheaply produce useful materials. CONSTITUTION: A silkworm egg for transformation is prepared by acid treatment of an egg of dormant state at 25 Deg. C. for one hour. A method for preparing a silkworm transformant comprises: a step of preparing the silkworm egg; a step of cloning a cassette vector to a basic vector in which a red fluorescent gene is introduced at 3XP promoter downstream and preparing a delivery system for silkworm transformation; and a step of microinjection of the delivery system to the silkworm egg. [Reference numerals] (AA) Hatching rate(%); (BB, DD) Untreated; (CC, EE) Micro-injection