A Vector Library for Silencing Central Carbon Metabolism Genes with Antisense RNAs in Escherichia coli

ABSTRACT We describe here the construction of a series of 71 vectors to silence central carbon metabolism genes in Escherichia coli. The vectors inducibly express antisense RNAs called paired-terminus antisense RNAs, which have a higher silencing efficacy than ordinary antisense RNAs. By measuring mRNA amounts, measuring activities of target proteins, or observing specific phenotypes, it was confirmed that all the vectors were able to silence the expression of target genes efficiently. Using this vector set, each of the central carbon metabolism genes was silenced individually, and the accumulation of metabolites was investigated. We were able to obtain accurate information on ways to increase the production of pyruvate, an industrially valuable compound, from the silencing results. Furthermore, the experimental results of pyruvate accumulation were compared to in silico predictions, and both sets of results were consistent. Compared to the gene disruption approach, the silencing approach has an advantage in that any E. coli strain can be used and multiple gene silencing is easily possible in any combination.

[1]  N. Nakashima,et al.  A new carbon catabolite repression mutation of Escherichia coli, mlc∗, and its use for producing isobutanol. , 2012, Journal of bioscience and bioengineering.

[2]  Alessandra Stefan,et al.  Shine-Dalgarno sequence enhances the efficiency of lacZ repression by artificial anti-lac antisense RNAs in Escherichia coli. , 2010, Journal of bioscience and bioengineering.

[3]  K. Shanmugam,et al.  Engineering Escherichia coli for efficient conversion of glucose to pyruvate. , 2004, Proceedings of the National Academy of Sciences of the United States of America.

[4]  J. Guest,et al.  Transcription analysis of the sucAB, aceEF and lpd genes of Escherichia coli , 2004, Molecular and General Genetics MGG.

[5]  S Pestka,et al.  Anti-mRNA: specific inhibition of translation of single mRNA molecules. , 1984, Proceedings of the National Academy of Sciences of the United States of America.

[6]  H. Mori,et al.  Construction of Escherichia coli K-12 in-frame, single-gene knockout mutants: the Keio collection , 2006, Molecular systems biology.

[7]  A. Kulyté,et al.  Variable coordination of cotranscribed genes in Escherichia coli following antisense repression , 2006, BMC Microbiology.

[8]  Tomohiro Tamura,et al.  Paired termini stabilize antisense RNAs and enhance conditional gene silencing in Escherichia coli , 2006, Nucleic acids research.

[9]  H. Fatania,et al.  Chemical modification of rat liver cytosolic NADP+‐linked isocitrate dehydrogenase by N‐ethylmaleimide Evidence for essential sulphydryl groups , 1993, FEBS letters.

[10]  A. Roe,et al.  Generation of gene deletions and gene replacements in Escherichia coli O157:H7 using a temperature sensitive allelic exchange system , 2006, Biological Procedures Online.

[11]  I. Beacham,et al.  Transcriptional co‐activation at the ansB promoters: involvement of the activating regions of CRP and FNR when bound in tandem , 1995, Molecular microbiology.

[12]  M. Bonete,et al.  Operation of glyoxylate cycle in halophilic archaea: presence of malate synthase and isocitrate lyase in Haloferax volcanii , 1998, FEBS letters.

[13]  K. Shanmugam,et al.  Dihydrolipoamide Dehydrogenase Mutation Alters the NADH Sensitivity of Pyruvate Dehydrogenase Complex of Escherichia coli K-12 , 2008, Journal of bacteriology.

[14]  B. Palsson,et al.  Constraining the metabolic genotype–phenotype relationship using a phylogeny of in silico methods , 2012, Nature Reviews Microbiology.

[15]  Tomohiro Tamura,et al.  Conditional gene silencing of multiple genes with antisense RNAs and generation of a mutator strain of Escherichia coli , 2009, Nucleic acids research.

[16]  J. Guest,et al.  Transcription and transcript processing in the sdhCDAB-sucABCD operon of Escherichia coli. , 1998, Microbiology.

[17]  M. Domach,et al.  Simple constrained‐optimization view of acetate overflow in E. coli , 1990, Biotechnology and bioengineering.

[18]  H. Zalkin,et al.  Nucleotide sequence of Escherichia coli pyrG encoding CTP synthetase. , 1986, The Journal of biological chemistry.

[19]  Masaru Tomita,et al.  Update on the Keio collection of Escherichia coli single-gene deletion mutants , 2009, Molecular systems biology.

[20]  K. Nagai,et al.  Increased production of pyruvic acid by Escherichia coli RNase G mutants in combination with cra mutations , 2007, Applied Microbiology and Biotechnology.

[21]  R. Wilde,et al.  Transcript analysis of the citrate synthase and succinate dehydrogenase genes of Escherichia coli K12. , 1986, Journal of general microbiology.

[22]  Chikara Furusawa,et al.  Development and experimental verification of a genome-scale metabolic model for Corynebacterium glutamicum , 2009, Microbial cell factories.

[23]  M. Quail,et al.  The pdhR–aceEF–lpd operon of Escherichia coli expresses the pyruvate dehydrogenase complex , 1994, Molecular microbiology.

[24]  Adam M. Feist,et al.  A genome-scale metabolic reconstruction for Escherichia coli K-12 MG1655 that accounts for 1260 ORFs and thermodynamic information , 2007, Molecular systems biology.

[25]  S. Busby,et al.  Regulation of Acetyl Coenzyme A Synthetase inEscherichia coli , 2000, Journal of bacteriology.

[26]  H. Shimizu,et al.  Pyruvic acid production by an F1-ATPase-defective mutant of Escherichia coli W1485lip2. , 1994, Bioscience, biotechnology, and biochemistry.

[27]  J. Cronan,et al.  Growth rate regulation of Escherichia coli acetyl coenzyme A carboxylase, which catalyzes the first committed step of lipid biosynthesis , 1993, Journal of bacteriology.

[28]  L. Good,et al.  Concurrent Growth Rate and Transcript Analyses Reveal Essential Gene Stringency in Escherichia coli , 2009, PloS one.

[29]  K. Shimizu,et al.  Global metabolic regulation analysis for Escherichia coli K12 based on protein expression by 2-dimensional electrophoresis and enzyme activity measurement , 2003, Applied Microbiology and Biotechnology.

[30]  J. Bongaerts,et al.  Transcriptional regulation of the proton translocating NADH dehydrogenase (nuoA‐N) of Escherichia coli by electron acceptors, electron donors and gene regulators , 1995, Molecular microbiology.

[31]  J. W. Campbell,et al.  Experimental Determination and System Level Analysis of Essential Genes in Escherichia coli MG1655 , 2003, Journal of bacteriology.

[32]  I. Blomfield,et al.  Allelic exchange in Escherichia coli using the Bacillus subtilis sacB gene and a temperature‐sensitive pSC101 replicon , 1991, Molecular microbiology.

[33]  Ali R. Zomorrodi,et al.  Mathematical optimization applications in metabolic networks. , 2012, Metabolic engineering.

[34]  J. Keasling Synthetic biology and the development of tools for metabolic engineering. , 2012, Metabolic engineering.

[35]  Adam M. Feist,et al.  A comprehensive genome-scale reconstruction of Escherichia coli metabolism—2011 , 2011, Molecular systems biology.

[36]  M. Araúzo-Bravo,et al.  Effect of a pyruvate kinase (pykF-gene) knockout mutation on the control of gene expression and metabolic fluxes in Escherichia coli. , 2004, FEMS microbiology letters.

[37]  Juhan Kim,et al.  Why metabolic enzymes are essential or nonessential for growth of Escherichia coli K12 on glucose. , 2007, Biochemistry.

[38]  P. Gröbner,et al.  Pyruvate formate-lyase of Escherichia coli: the acetyl-enzyme intermediate. , 1974, European journal of biochemistry.

[39]  T. Inada,et al.  Expression of the glucose transporter gene, ptsG, is regulated at the mRNA degradation step in response to glycolytic flux in Escherichia coli , 2001, The EMBO journal.

[40]  K. Shanmugam,et al.  Pyruvate Formate Lyase and Acetate Kinase Are Essential for Anaerobic Growth of Escherichia coli on Xylose , 2004, Journal of bacteriology.

[41]  Scott K. Johnson,et al.  Characterization of a maize cDNA that complements an enolase-deficient mutant of Escherichia coli , 1991, Plant Molecular Biology.

[42]  R. Gunsalus,et al.  Effect of microaerophilic cell growth conditions on expression of the aerobic (cyoABCDE and cydAB) and anaerobic (narGHJI, frdABCD, and dmsABC) respiratory pathway genes in Escherichia coli , 1996, Journal of bacteriology.

[43]  J. Bailey,et al.  Effects of recombinant plasmid content on growth properties and cloned gene product formation in Escherichia coli , 1985, Biotechnology and bioengineering.

[44]  B. Washburn,et al.  New method for generating deletions and gene replacements in Escherichia coli , 1989, Journal of bacteriology.

[45]  S. Park,et al.  Transcriptional regulation of the proton-translocating ATPase (atpIBEFHAGDC) operon of Escherichia coli: control by cell growth rate , 1996, Journal of bacteriology.

[46]  M. A. Eiteman,et al.  The effect of acetate pathway mutations on the production of pyruvate in Escherichia coli , 2003, Applied Microbiology and Biotechnology.

[47]  A. Brandelli,et al.  Influence of growth conditions on bacteriocin production by Brevibacterium linens , 2003, Applied Microbiology and Biotechnology.

[48]  J. Abrahams,et al.  Prediction of RNA secondary structure, including pseudoknotting, by computer simulation. , 1990, Nucleic acids research.

[49]  R. Gennis,et al.  Cytochrome o (cyoABCDE) and d (cydAB) oxidase gene expression in Escherichia coli is regulated by oxygen, pH, and the fnr gene product , 1990, Journal of bacteriology.