Production of intracellular heparosan and derived oligosaccharides by lyase expression in metabolically engineered E. coli K-12

被引:38
作者
Barreteau, Helene [1 ]
Richard, Emeline [1 ]
Drouillard, Sophie [1 ]
Samain, Eric [1 ]
Priem, Bernard [1 ]
机构
[1] CNRS, Ctr Rech Macromol Vegetales, Grp Chim & Biotechnol Oligosaccharides, F-38041 Grenoble 09, France
关键词
Glycosaminoglycans; E; coli; K5; polysaccharide; Heparosan; Lyase; Metabolic engineering; ESCHERICHIA-COLI; CAPSULAR POLYSACCHARIDE; K5; POLYSACCHARIDE; GENE-CLUSTER; CLONING; HEPARIN; VECTORS;
D O I
10.1016/j.carres.2012.07.013
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The cluster of genes of capsular K5 heparosan is composed of three regions, involved in the synthesis and the exportation of the polysaccharide. The region 2 possesses all the necessary genes involved in the synthesis of heparosan, namely kfiA, encoding alpha-4-N-acetylglucosaminyltransferase, kfiD, encoding beta-3-glucuronyl transferase, kfiC, encoding UDP-glucose dehydrogenase (UDP-glucuronic acid synthesis), and kfiB encoding a protein of unknown function. The cloning and expression of kfiADCB into Escherichia coli K-12 were found to be sufficient for the production of heparosan, which accumulates in the cells due to a lack of the exporting system. The concentration of recombinant heparosan reached one gram per liter under fed-batch cultivation. The cytoplasmic localization of heparosan inside the bacteria allowed subsequent enzymatic modifications such as a partial degradation with K5 lyase when expressed intracellularly. Under these conditions, the production of DP 2-10 oligosaccharides occurred intracellularly, at a concentration similar to that of recombinant intracellular heparosan. (C) 2012 Elsevier Ltd. All rights reserved.
引用
收藏
页码:19 / 24
页数:6
相关论文
共 23 条
[1]   NEW METHOD FOR QUANTITATIVE-DETERMINATION OF URONIC ACIDS [J].
BLUMENKR.N ;
ASBOEHAN.G .
ANALYTICAL BIOCHEMISTRY, 1973, 54 (02) :484-489
[2]  
BRONNER D, 1993, FEMS MICROBIOL LETT, V113, P279, DOI 10.1111/j.1574-6968.1993.tb06527.x
[3]   EXPRESSION OF THE CAPSULAR K5 POLYSACCHARIDE OF ESCHERICHIA-COLI - BIOCHEMICAL AND ELECTRON-MICROSCOPIC ANALYSES OF MUTANTS WITH DEFECTS IN REGION-1 OF THE K5 GENE-CLUSTER [J].
BRONNER, D ;
SIEBERTH, V ;
PAZZANI, C ;
ROBERTS, IS ;
BOULNOIS, GJ ;
JANN, B ;
JANN, K .
JOURNAL OF BACTERIOLOGY, 1993, 175 (18) :5984-5992
[4]   HEPARIN-LIKE COMPOUNDS PREPARED BY CHEMICAL MODIFICATION OF CAPSULAR POLYSACCHARIDE FROM ESCHERICHIA-COLI K5 [J].
CASU, B ;
GRAZIOLI, G ;
RAZI, N ;
GUERRINI, M ;
NAGGI, A ;
TORRI, G ;
ORESTE, P ;
TURSI, F ;
ZOPPETTI, G ;
LINDAHL, U .
CARBOHYDRATE RESEARCH, 1994, 263 (02) :271-284
[5]   Identification of a distinct, cryptic heparosan synthase from Pasteurella multocida types A, D, and F [J].
DeAngelis, PL ;
White, CL .
JOURNAL OF BACTERIOLOGY, 2004, 186 (24) :8529-8532
[6]   A colorimetric method for the determination of glucosamine and chondrosamine. [J].
Elson, LA ;
Morgan, WTJ .
BIOCHEMICAL JOURNAL, 1933, 27 :1824-1828
[7]   The Escherichia coli K5 Capsule Is Not Synthesized in a Protected Compartment within the Cytoplasm [J].
Hudson, Thomas ;
Goldrick, Marie ;
Roberts, Ian S. .
JOURNAL OF BACTERIOLOGY, 2009, 191 (05) :1716-1718
[8]   4 NEW DERIVATIVES OF THE BROAD-HOST-RANGE CLONING VECTOR PBBR1MCS, CARRYING DIFFERENT ANTIBIOTIC-RESISTANCE CASSETTES [J].
KOVACH, ME ;
ELZER, PH ;
HILL, DS ;
ROBERTSON, GT ;
FARRIS, MA ;
ROOP, RM ;
PETERSON, KM .
GENE, 1995, 166 (01) :175-176
[9]   BIOSYNTHESIS OF HEPARIN - USE OF ESCHERICHIA-COLI K5 CAPSULAR POLYSACCHARIDE AS A MODEL SUBSTRATE IN ENZYMATIC POLYMER-MODIFICATION REACTIONS [J].
KUSCHE, M ;
HANNESSON, HH ;
LINDAHL, U .
BIOCHEMICAL JOURNAL, 1991, 275 :151-158
[10]   N-acetyl-heparosan lyase of Escherichia coli K5: Gene cloning and expression [J].
Legoux, R ;
Lelong, P ;
Jourde, C ;
Feuillerat, C ;
Capdevielle, J ;
Sure, V ;
Ferran, E ;
Kaghad, M ;
Delpech, B ;
Shire, D ;
Ferrara, P ;
Loison, G ;
Salome, M .
JOURNAL OF BACTERIOLOGY, 1996, 178 (24) :7260-7264