Antibacterial vaccine composition
    1.
    发明专利
    Antibacterial vaccine composition 审中-公开
    抗生素疫苗组合物

    公开(公告)号:JP2011097938A

    公开(公告)日:2011-05-19

    申请号:JP2010247585

    申请日:2010-11-04

    CPC分类号: C07K14/285 A61K2039/522

    摘要: PROBLEM TO BE SOLVED: To identify a pathogenic gene of gram-negative bacterium, thereby allowing the identification of a new antibacterial agent that targets the pathogenic gene and a product thereof, and to provide a new gram-negative bacterial mutant useful in vaccines.
    SOLUTION: An attenuated Pasteurella (Mannheimia) haemolytica bacterium is provided, being such that: a mutation is introduced into a gene represented by a polynucleotide sequence encoding atpG polypeptide to effect modification so as to decline in the expression of a gene product encoded by the gene and cause the expression of an inactive gene product. Besides, an immunogenic composition and a vaccine composition each containing the gene are also provided.
    COPYRIGHT: (C)2011,JPO&INPIT

    摘要翻译: 要解决的问题:为了鉴定革兰氏阴性细菌的致病基因,从而允许鉴定靶向致病基因的新抗菌剂及其产物,并提供可用于新鲜革兰氏阴性菌的新型革兰氏阴性细菌突变体 疫苗。 解决方案:提供减毒巴斯德氏菌(Mannheimia)溶血霉菌,使得:将突变引入到由编码atpG多肽的多核苷酸序列表示的基因中进行修饰,以使编码的基因产物的表达下降 通过该基因导致无活性基因产物的表达。 此外,还提供了各自含有该基因的免疫原性组合物和疫苗组合物。 版权所有(C)2011,JPO&INPIT

    3-(CONDENSED RING-SUBSTITUTED) PHENYL-5BETA-AMIDOMETHYLOXAZOLIDIN-2-ONES AND 3-(NITROGEN ATOM-SUBSTITUTED) PHENYL-5BETA-AMIDOMETHYLOXAZOLIDIN-2-ONES

    公开(公告)号:JPH1180139A

    公开(公告)日:1999-03-26

    申请号:JP19194998

    申请日:1998-07-07

    申请人: UPJOHN CO

    发明人: BRICKNER STEVEN J

    摘要: PROBLEM TO BE SOLVED: To obtain a new 3-(condensed ring-substituted) phenyl-5β- amidomethyloxazolidinone useful as an antimicrobial agent. SOLUTION: This 3-(condensed ring-substituted) phenyl-5β-(amidomethyl) oxazolidin-2-one is shown by formula I [R1 is H, an alkyl, a cycloalkyl, an alkenyl, phenyl, pyridyl, etc.; either R2 or R4 is H and the other and R3 form a group of formula II (n3 and n4 are each 0-3; n7 and n are each 0 or 1; R10-1 and R10-2 are each H, an alkyl, etc.; R10-3 and R10-4 are each as shown for R10-1 and R10-2 ), etc.; either R5 or R6 is H and the other is H, an alkyl, etc.], and its pharmaceutically permissible salt such as 3-(1'-oxo-2'α-methyl-5'- indanyl)-5β-(acetamidomethyl)oxazolidin-2-one. The compound of formula I is prepared by obtaining a compound of formula IV through three processes from a compound of formula III, then forming a compound of formula V, reducing the compound with H2 and further acylating the resulting compound.

    COMPOSITION CONTAINING 3-GUANIDINOPROPIONIC ACID

    公开(公告)号:JPH0820534A

    公开(公告)日:1996-01-23

    申请号:JP17854695

    申请日:1995-07-14

    申请人: UPJOHN CO

    摘要: PROBLEM TO BE SOLVED: To obtain a composition for reducing the fat content of the farm animals, and increasing the muscle and protein contents thereof. SOLUTION: This composition consists of 3-guanidinopropionic acid or medically acceptable salts thereof in an effective amount, and is used for producing an animal product having less fat content. The composition is administered by mixing with a feed, or by injecting or using a mobile sustained release apparatus. By the administration of 3-guanidinopropionic acid, it is possible to treat or prevent certain kinds of metabolic disorders in humans and animals e.g. hyperglycemia, glucose tolerance disorder, hyperinsulinemia, insulin insensitivity, hypermylinemia, adposis or hyperlipidemia.