发明名称 Viable gram negative bacteria lacking outer membrane agonists of TLR4/MD-2
摘要 Viable Gram-negative bacteria or components thereof comprising outer membranes that substantially lack a ligand, such as Lipid A or 6-acyl lipidpolysaccharide, that acts as an agonist of TLR4/MD2. The bacteria may comprise reduced activity of arabinose-5-phosphate isomerases and one or more suppressor mutations, for example in a transporter thereby increasing the transporters capacity to transport Lipid IVA or in membrane protein YhjD. One or more genes (e.g., IpxL, IpxM, pagP, IpxP, and/or eptA) may be substantially deleted and/or one or more enzymes (e.g., LpxL, LpxM, PagP, LpxP, and/or EptA) may be substantially inactive. The bacteria may be competent to take up extracellular DNA, may be donor bacteria, or may be members of a library. The present invention also features methods of creating and utilizing such bacteria.
申请公布号 US9068186(B2) 申请公布日期 2015.06.30
申请号 US201113046562 申请日期 2011.03.11
申请人 RESEARCH CORPORATION TECHNOLOGIES, INC. 发明人 Bramhill David;Mamat Uwe
分类号 C12N1/20;C12N15/70;C12N15/10;C12N15/78;C12P19/34;C12P21/02;C40B40/02 主分类号 C12N1/20
代理机构 Scully, Scott, Murphy & Presser, P.C. 代理人 Scully, Scott, Murphy & Presser, P.C.
主权项 1. An isolated, viable, non-conditional, Gram-negative mutant bacterium, wherein said bacterium is Escherichia coli and comprises an outer membrane that substantially lacks a ligand that acts as an agonist of a human TLR4/MD-2 receptor, said ligand comprising lipid A, wherein the bacterium comprises (a) a mutation in at least one of the genes selected from the group consisting of kdsA, kdsC, kdsB, and waaA, or a mutation in each of the kdsD and gutQ genes, wherein said mutation results in a disruption in the biosynthesis of (Kdo)2-lipid IVA, (b) a mutation in each of the genes pagP and eptA wherein said mutation substantially inactivates the enzymatic activity of each of the proteins encoded by the pagP and eptA genes, and (c) a suppressor mutation in the msbA gene resulting in an increased capacity of the encoded MsbA protein to transport lipid IVA.
地址 Tucson AZ US