Abstract:
목적: 본 발명은 뇌척수액이 누수되지 않고, 종래 인공경막과는 달리 생체적합성이 우수하여 세포독성이 없고 수술시 염증을 유발하지 않으면서 투명하여 수술시 안전성을 담보할 수 있는 실크피브로인을 주요 구성 요소로 하는 인공경막을 제공하는 것이다. 방법: 본 발명자들은 누에( Bombyx mori )로부터 얻은 실크 피브로인을 이용하여 투명한 인공 뇌경막을 제조하였고, 인비트로 및 인비보에서 세포독성 및 염증저해효과를 시험하였다. 실크 피브로인 인공 뇌경막을 가지고 뇌경막재생수술을 동물 모델에 실시하였다. 염증은 조직학적 시험 및 웨스턴 블랏팅으로 측정하였다. 본 발명의 실크 피브로인을 이용한 새로운 인공 뇌경막은 세포 내에서 세포 독성을 나타내지 않았고, 래트에서 일반적인 종래의 뇌경막 재료인 음성대조군과 비교하여 차이가 없었다. 또한, 실크 피브로인 뇌경막은 래트에서 COX-2와 iNOS 발현을 효과적으로 감소시켰다.
Abstract:
PURPOSE: A method for preparing a large amount of papiliocin using recombinant E.coli is provided to ensure high antibacterial activity against various bacteria. CONSTITUTION: A recombinant expression vector pET-KSI/papiliocin contains papiliocin gene. The gene is derived from Papilio xuthus larva. The E.coli BL21(DE3) is prepared by transforming by papiliocin gene-containing recombinant expression vector pET-KSI/Papiliocin. A method for preparing a large amount of recombinant papiliocin comprises: a step of preparing transformed recombinant E.coli; a step of culturing the transformed E.coli to express insoluble recombinant fusion protein; and a step of collecting papiliocin. A pharmaceutical composition for antibiotics contains the recombinant papiliocin as an active ingredient.
Abstract:
PURPOSE: An artificial eardrum using a silk protein and a method for manufacturing the same are provided to have strengths in bio compatibility and transparency. CONSTITUTION: An artificial eardrum using a silk protein comprises a silk film shape by desalinating and drying silk protein or silk protein compound solution obtained after removing ceracin from cocoons or fibroin Silk protein or silk protein compound solution are dissolved using chaotropic salt or one compound of bromination lithium, lithium chloride, zinc chloride, or calcium chloride. At least one additive of gelatin, collagen, chitosan, alginic acid, hyaluronic acid, pluronic 127 or PEG is added to the silk film.
Abstract:
PURPOSE: A novel antibacterial peptide gene and antibacterial peptide isolated from Papilio xuthus larva are provided to ensure antibacterial activity against fungi causing candidiasis. CONSTITUTION: An antibacterial peptide gene isolated from Papilio xuthus larva has a base sequence of sequence number 1. An antibacterial peptide encoded by the gene of sequence number 1 has an amino acid sequence of sequence number 2. A pharmaceutical composition contains the antibacterial peptide of sequence number 2 or 3 as an active ingredient.
Abstract:
A promoter and entire genome sequence of heat shock protein isolated from a silk worm is provided to express a excess amount foreign gene and easily select transformant of silk worm. A gene sequence of heat shock protein 70 gene denoted by the sequence 1 comprises gene area and promoter area of heat shock protein 70 isolated silk worm. The Cdna sequence of heat shock protein 70 is denoted by the sequence 2. The amino acid sequence denoted by the sequenc 3 is deduced by cDNA sequence. The maximum promoter activation area of heat shock protein 70 gene comprises 367-1517 sequences.
Abstract:
Provided is a method for discriminating domestic silkworm powder from imported silkworm powder through direct base sequencing analysis. Nine introns are used as silkworm discrimination markers. The nine introns indicate A4Intron1, A4Intron2, PTTHIntron3, LCP30Intron3, LCP30Intron4, SPIIntron3, VDPIntron4, FLCIntron3 and XDHIntron3. A method for discriminating domestic silkworm powder using the direct base sequencing analysis comprises the following steps of: extracting a genome DNA from the silkworm powder; offering information about DNA amplification existence or nonexistence in a specific intron region through PCR(polymerase chain reaction); offering information about discriminable intron regions based on species and primer in the regions through the direct base sequencing analysis; and comparing the species in the intron regions using the silkworm discrimination marker.
Abstract:
A novel sequence and an antibacterial peptide isolated from larvae of Copris tripartitus are provided to be usefully used as a prophylactic and therapeutic agent of bacterial diseases of human and plant and show antibacterial activity against various pathogenic bacteria. A sequence of an antibacterial peptide isolated from larvae of Copris tripartitus(SEQ ID : NO. 3) is represented by the following : AACGGTTCTG AATTCTTAAC CAGTTCATAC CCAGCTATAA TTTGAATTAC 50 GTCTTTTAAA AAGATGGCAA AATTAATTGC TTTTGCATTA GTAGCTTCGT 100 TATGCCTGTC TATGGTGTTG TGCAATCCGT TACCAGAAGA AGTCCAAGAA 150 GAGGGACTTG TCAGACAAAA AAGGGTAACC TGTGACGTGT TAAGTTTCGA 200 AGCCAAAGGA ATAGCTGTAA ATCATTCGGC TTGTGCGCTA CATTGTATTG 250 CCTTACGTAA AAAAGGTGGT TCTTGTCAAA ATGGTGTGTG TGTTTGTAGA 300 AATTAATTAA CAAGCTGATT GTCCTTTTTT TTAATTGTGG CCGGATGATA 350 TTATTTTCAG TGTAATAAGA ACAAAAATAA AGATTTATAA CTATTAAAAA 400 AAAAAAAAAA AA 412. A novel antibacterial peptide(SEQ ID : NO. 4) is encoded by the sequence and consists of an amino acid sequence of Met Ala Lys Leu Ile Ala Phe Ala Leu Val Ala Ser Leu Cys Leu 15 Ser Met Val Leu Cys Asn Pro Leu Pro Glu Glu Val Gln Glu Glu 30 Gly Leu Val Arg Gln Lys Arg Val Thr Cys Asp Val Leu Ser Phe 45 Glu Ala Lys Gly Ile Ala Val Asn His Ser Ala Cys Ala Leu His 60 Cys Ile Ala Leu Arg Lys Lys Gly Gly Ser Cys Gln Asn Gly Val 75 Cys Val Cys Arg Asn 80.
Abstract translation:提供从Copris triartae的幼虫分离的新的序列和抗菌肽,有效地用作人和植物的细菌性疾病的预防和治疗剂,并且对各种致病菌具有抗菌活性。 (SEQ ID:NO 3)从Copris tripartitus的幼虫中分离的抗菌肽的序列:AACGGTTCTG AATTCTTAAC CAGTTCATAC CCAGCTATAA TTTGAATTAC 50 GTCTTTTAAA AAGATGGCAA AATTAATTGC TTTTGCATTA GTAGCTTCGT 100 TATGCCTGTC TATGGTGTTG TGCAATCCGT TACCAGAAGA AGTCCAAGAA 150 GAGGGACTTG TCAGACAAAA AAGGGTAACC TGTGACGTGT TAAGTTTCGA 200由下式表示 AGCCAAAGGA ATAGCTGTAA ATCATTCGGC TTGTGCGCTA CATTGTATTG 250 CCTTACGTAA AAAAGGTGGT TCTTGTCAAA ATGGTGTGTG TGTTTGTAGA 300 AATTAATTAA CAAGCTGATT GTCCTTTTTT TTAATTGTGG CCGGATGATA 350 TTATTTTCAG TGTAATAAGA ACAAAAATAA AGATTTATAA CTATTAAAAA 400 AAAAAAAAAA AA 412的新型抗菌肽(SEQ ID:NO:4)是由序列编码,由一个氨基的 Met Ala Lys Leu的氨基酸序列Ile Ala Phe Ala Leu Val Ala Ser Leu Cys Leu 15 Ser Met Val Leu Cys Asn Pro Leu Pro Glu Glu Val Gln Glu Glu 30 Gly Leu Val Arg Gln Lys Arg Val Thr Cys Asp Val Leu Ser Phe 45 Glu Ala Lys Gly Ile Ala Val Asn His Ser Ala Cys Ala Leu His 60 Cys Ile Ala Leu Arg Lys Lys Gly Gly Ser Cys Gln Asn Gly Val 75 Cys Val Cys Arg Asn 80。
Abstract:
A method for preserving pupa infected with Cordyceps spp, entomopathogenic fungi for a long time and a method for regenerating the fungi are provided to dispense with an expensive equipment or high technology for preserving the fungi, and also to produce fruit bodies on consumer demands by taking out the preserved pupa at desired time. The cultivation time of Cordyceps spp, entomopathogenic fungi can be controlled voluntarily, thereby solving the concentration of production time and the surplus or stock of production. A long-term preserving method of pupa infected with Cordyceps spp, entomopathogenic fungi comprises: preparing the pupa infected with Cordyceps spp, entomopathogenic fungi, controlling the water content of the pupa body to 4%, and then preserving the pupa at 4°C or less, or at -70°C after freeze-drying. The fungi regenerating method comprises soaking the preserved pupa in distilled water for 1~3hr, followed by saturating the pupa with water. The infected pupa can be preserved stably in a water content of 4% at a storage temperature of 4°C or less for 135day, and the regeneration ratio is to about 97%. In addition, a preservation period is more increased at lower temperature in freezing, and is up to 1year in preserving at -70°C or less after freeze-drying.
Abstract:
PURPOSE: Provided are a nucleotide sequence of cDNA coding protein disulfide isomerase(PDI) isolated from the cultured cell of a silkworm, and an amino acid sequence thereof, thereby increasing the expression of useful proteins and consequently mass-producing them economically. CONSTITUTION: The nucleotide sequence of cDNA coding protein disulfide isomerase(PDI) isolated from the cultured cell of a silkworm, is represented by the SEQ ID NO:1, and its amino acid sequence is represented by the SEQ ID NO:2.
Abstract translation:目的:提供从蚕的培养细胞分离的cDNA编码蛋白质二硫键异构酶(PDI)的核苷酸序列及其氨基酸序列,从而增加有用蛋白质的表达,从而经济地批量生产它们。 构成:从蚕的培养细胞分离的cDNA编码蛋白质二硫键异构酶(PDI)的核苷酸序列由SEQ ID NO:1表示,其氨基酸序列由SEQ ID NO:2表示。