ALBERT

All Library Books, journals and Electronic Records Telegrafenberg

feed icon rss

Your email was sent successfully. Check your inbox.

An error occurred while sending the email. Please try again.

Proceed reservation?

Export
  • 1
    Publication Date: 2014-04-15
    Description: Selection has been invaluable for genetic manipulation, although counter-selection has historically exhibited limited robustness and convenience. TolC, an outer membrane pore involved in transmembrane transport in E. coli , has been implemented as a selectable/counter-selectable marker, but counter-selection escape frequency using colicin E1 precludes using tolC for inefficient genetic manipulations and/or with large libraries. Here, we leveraged unbiased deep sequencing of 96 independent lineages exhibiting counter-selection escape to identify loss-of-function mutations, which offered mechanistic insight and guided strain engineering to reduce counter-selection escape frequency by ~40-fold. We fundamentally improved the tolC counter-selection by supplementing a second agent, vancomycin, which reduces counter-selection escape by 425-fold, compared colicin E1 alone. Combining these improvements in a mismatch repair proficient strain reduced counter-selection escape frequency by 1.3E6-fold in total, making tolC counter-selection as effective as most selectable markers, and adding a valuable tool to the genome editing toolbox. These improvements permitted us to perform stable and continuous rounds of selection/counter-selection using tolC , enabling replacement of 10 alleles without requiring genotypic screening for the first time. Finally, we combined these advances to create an optimized E. coli strain for genome engineering that is ~10-fold more efficient at achieving allelic diversity than previous best practices.
    Print ISSN: 0305-1048
    Electronic ISSN: 1362-4962
    Topics: Biology
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 2
    Publication Date: 2009-07-28
    Description: The breadth of genomic diversity found among organisms in nature allows populations to adapt to diverse environments. However, genomic diversity is difficult to generate in the laboratory and new phenotypes do not easily arise on practical timescales. Although in vitro and directed evolution methods have created genetic variants with usefully altered phenotypes, these methods are limited to laborious and serial manipulation of single genes and are not used for parallel and continuous directed evolution of gene networks or genomes. Here, we describe multiplex automated genome engineering (MAGE) for large-scale programming and evolution of cells. MAGE simultaneously targets many locations on the chromosome for modification in a single cell or across a population of cells, thus producing combinatorial genomic diversity. Because the process is cyclical and scalable, we constructed prototype devices that automate the MAGE technology to facilitate rapid and continuous generation of a diverse set of genetic changes (mismatches, insertions, deletions). We applied MAGE to optimize the 1-deoxy-D-xylulose-5-phosphate (DXP) biosynthesis pathway in Escherichia coli to overproduce the industrially important isoprenoid lycopene. Twenty-four genetic components in the DXP pathway were modified simultaneously using a complex pool of synthetic DNA, creating over 4.3 billion combinatorial genomic variants per day. We isolated variants with more than fivefold increase in lycopene production within 3 days, a significant improvement over existing metabolic engineering techniques. Our multiplex approach embraces engineering in the context of evolution by expediting the design and evolution of organisms with new and improved properties.〈br /〉〈br /〉〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4590770/" target="_blank"〉〈img src="https://static.pubmed.gov/portal/portal3rc.fcgi/4089621/img/3977009" border="0"〉〈/a〉   〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4590770/" target="_blank"〉This paper as free author manuscript - peer-reviewed and accepted for publication〈/a〉〈br /〉〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Wang, Harris H -- Isaacs, Farren J -- Carr, Peter A -- Sun, Zachary Z -- Xu, George -- Forest, Craig R -- Church, George M -- DP5 OD009172/OD/NIH HHS/ -- England -- Nature. 2009 Aug 13;460(7257):894-8. doi: 10.1038/nature08187. Epub 2009 Jul 26.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Genetics, Harvard Medical School, Boston, Massachusetts 02115, USA. hhwang@genetics.med.harvard.edu〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/19633652" target="_blank"〉PubMed〈/a〉
    Keywords: Alleles ; Biotechnology/instrumentation/*methods ; Carotenoids/biosynthesis ; Chromosomes, Bacterial/genetics ; DNA/biosynthesis/genetics ; Directed Molecular Evolution/instrumentation/*methods ; Escherichia coli/cytology/*genetics/*metabolism ; Genetic Variation/genetics ; Genome, Bacterial/*genetics ; Pentosephosphates/biosynthesis
    Print ISSN: 0028-0836
    Electronic ISSN: 1476-4687
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 3
    Publication Date: 2013-10-19
    Description: We describe the construction and characterization of a genomically recoded organism (GRO). We replaced all known UAG stop codons in Escherichia coli MG1655 with synonymous UAA codons, which permitted the deletion of release factor 1 and reassignment of UAG translation function. This GRO exhibited improved properties for incorporation of nonstandard amino acids that expand the chemical diversity of proteins in vivo. The GRO also exhibited increased resistance to T7 bacteriophage, demonstrating that new genetic codes could enable increased viral resistance.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Lajoie, Marc J -- Rovner, Alexis J -- Goodman, Daniel B -- Aerni, Hans-Rudolf -- Haimovich, Adrian D -- Kuznetsov, Gleb -- Mercer, Jaron A -- Wang, Harris H -- Carr, Peter A -- Mosberg, Joshua A -- Rohland, Nadin -- Schultz, Peter G -- Jacobson, Joseph M -- Rinehart, Jesse -- Church, George M -- Isaacs, Farren J -- 1DP5OD009172-01/OD/NIH HHS/ -- DP5 OD009172/OD/NIH HHS/ -- K01 DK089006/DK/NIDDK NIH HHS/ -- K01DK089006/DK/NIDDK NIH HHS/ -- T32 GM007205/GM/NIGMS NIH HHS/ -- T32GM07205/GM/NIGMS NIH HHS/ -- New York, N.Y. -- Science. 2013 Oct 18;342(6156):357-60. doi: 10.1126/science.1241459.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Genetics, Harvard Medical School, Boston, MA 02115, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/24136966" target="_blank"〉PubMed〈/a〉
    Keywords: Amino Acid Substitution/genetics ; Amino Acids/*genetics ; Bacteriophage T7/*physiology ; Codon, Terminator/*genetics ; Escherichia coli/*genetics/*virology ; Escherichia coli Proteins/genetics ; Genetic Engineering ; Genome, Bacterial ; Organisms, Genetically Modified/*genetics/*virology ; Peptide Chain Termination, Translational/genetics ; Peptide Termination Factors/genetics
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 4
    Publication Date: 2005-03-26
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Isaacs, Farren J -- Blake, William J -- Collins, James J -- New York, N.Y. -- Science. 2005 Mar 25;307(5717):1886-8.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Lipper Center for Computational Genetics and Department of Genetics, Harvard Medical School, Boston, MA 02115, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15790834" target="_blank"〉PubMed〈/a〉
    Keywords: Bacterial Proteins/biosynthesis/metabolism ; DNA-Binding Proteins/genetics/metabolism ; Escherichia coli/*genetics ; Escherichia coli Proteins/*metabolism ; Feedback, Physiological ; *Gene Expression Regulation, Bacterial ; Green Fluorescent Proteins/biosynthesis ; Lac Repressors ; Luminescent Proteins/biosynthesis ; *Models, Genetic ; Repressor Proteins/genetics/metabolism ; Signal Transduction ; Stochastic Processes ; Transcription Factors/*metabolism ; Viral Proteins ; Viral Regulatory and Accessory Proteins
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 5
    Publication Date: 2011-07-19
    Description: We present genome engineering technologies that are capable of fundamentally reengineering genomes from the nucleotide to the megabase scale. We used multiplex automated genome engineering (MAGE) to site-specifically replace all 314 TAG stop codons with synonymous TAA codons in parallel across 32 Escherichia coli strains. This approach allowed us to measure individual recombination frequencies, confirm viability for each modification, and identify associated phenotypes. We developed hierarchical conjugative assembly genome engineering (CAGE) to merge these sets of codon modifications into genomes with 80 precise changes, which demonstrate that these synonymous codon substitutions can be combined into higher-order strains without synthetic lethal effects. Our methods treat the chromosome as both an editable and an evolvable template, permitting the exploration of vast genetic landscapes.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Isaacs, Farren J -- Carr, Peter A -- Wang, Harris H -- Lajoie, Marc J -- Sterling, Bram -- Kraal, Laurens -- Tolonen, Andrew C -- Gianoulis, Tara A -- Goodman, Daniel B -- Reppas, Nikos B -- Emig, Christopher J -- Bang, Duhee -- Hwang, Samuel J -- Jewett, Michael C -- Jacobson, Joseph M -- Church, George M -- K99 GM081450/GM/NIGMS NIH HHS/ -- R00 GM081450/GM/NIGMS NIH HHS/ -- New York, N.Y. -- Science. 2011 Jul 15;333(6040):348-53. doi: 10.1126/science.1205822.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Genetics, Harvard Medical School, Boston, MA 02115, USA. farren.isaacs@yale.edu〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/21764749" target="_blank"〉PubMed〈/a〉
    Keywords: Chromosomes, Bacterial/*genetics ; *Codon, Terminator ; *Conjugation, Genetic ; Directed Molecular Evolution ; Escherichia coli/*genetics/growth & development/physiology ; Genetic Engineering/*methods ; *Genome, Bacterial ; Genomic Instability ; Mutagenesis, Site-Directed ; Mutation ; Phenotype ; Recombination, Genetic ; Templates, Genetic
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 6
    Publication Date: 2015-09-30
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Rovner, Alexis J -- Haimovich, Adrian D -- Katz, Spencer R -- Li, Zhe -- Grome, Michael W -- Gassaway, Brandon M -- Amiram, Miriam -- Patel, Jaymin R -- Gallagher, Ryan R -- Rinehart, Jesse -- Isaacs, Farren J -- England -- Nature. 2015 Nov 12;527(7577):264. doi: 10.1038/nature15537. Epub 2015 Sep 23.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/26416756" target="_blank"〉PubMed〈/a〉
    Print ISSN: 0028-0836
    Electronic ISSN: 1476-4687
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 7
    Publication Date: 2015-01-22
    Description: Genetically modified organisms (GMOs) are increasingly used in research and industrial systems to produce high-value pharmaceuticals, fuels and chemicals. Genetic isolation and intrinsic biocontainment would provide essential biosafety measures to secure these closed systems and enable safe applications of GMOs in open systems, which include bioremediation and probiotics. Although safeguards have been designed to control cell growth by essential gene regulation, inducible toxin switches and engineered auxotrophies, these approaches are compromised by cross-feeding of essential metabolites, leaked expression of essential genes, or genetic mutations. Here we describe the construction of a series of genomically recoded organisms (GROs) whose growth is restricted by the expression of multiple essential genes that depend on exogenously supplied synthetic amino acids (sAAs). We introduced a Methanocaldococcus jannaschii tRNA:aminoacyl-tRNA synthetase pair into the chromosome of a GRO derived from Escherichia coli that lacks all TAG codons and release factor 1, endowing this organism with the orthogonal translational components to convert TAG into a dedicated sense codon for sAAs. Using multiplex automated genome engineering, we introduced in-frame TAG codons into 22 essential genes, linking their expression to the incorporation of synthetic phenylalanine-derived amino acids. Of the 60 sAA-dependent variants isolated, a notable strain harbouring three TAG codons in conserved functional residues of MurG, DnaA and SerS and containing targeted tRNA deletions maintained robust growth and exhibited undetectable escape frequencies upon culturing approximately 10(11) cells on solid media for 7 days or in liquid media for 20 days. This is a significant improvement over existing biocontainment approaches. We constructed synthetic auxotrophs dependent on sAAs that were not rescued by cross-feeding in environmental growth assays. These auxotrophic GROs possess alternative genetic codes that impart genetic isolation by impeding horizontal gene transfer and now depend on the use of synthetic biochemical building blocks, advancing orthogonal barriers between engineered organisms and the environment.〈br /〉〈br /〉〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4590768/" target="_blank"〉〈img src="https://static.pubmed.gov/portal/portal3rc.fcgi/4089621/img/3977009" border="0"〉〈/a〉   〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4590768/" target="_blank"〉This paper as free author manuscript - peer-reviewed and accepted for publication〈/a〉〈br /〉〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Rovner, Alexis J -- Haimovich, Adrian D -- Katz, Spencer R -- Li, Zhe -- Grome, Michael W -- Gassaway, Brandon M -- Amiram, Miriam -- Patel, Jaymin R -- Gallagher, Ryan R -- Rinehart, Jesse -- Isaacs, Farren J -- K01 DK089006/DK/NIDDK NIH HHS/ -- T32 GM007205/GM/NIGMS NIH HHS/ -- T32GM07205/GM/NIGMS NIH HHS/ -- England -- Nature. 2015 Feb 5;518(7537):89-93. doi: 10.1038/nature14095. Epub 2015 Jan 21.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉1] Department of Molecular, Cellular and Developmental Biology, Yale University, New Haven, Connecticut 06520, USA [2] Systems Biology Institute, Yale University, West Haven, Connecticut 06516, USA. ; 1] Systems Biology Institute, Yale University, West Haven, Connecticut 06516, USA [2] Department of Cellular and Molecular Physiology, Yale University, New Haven, Connecticut 06520, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/25607356" target="_blank"〉PubMed〈/a〉
    Keywords: Amino Acids/*chemical synthesis/chemistry/metabolism/*pharmacology ; Amino Acyl-tRNA Synthetases/genetics/metabolism ; Catalytic Domain/genetics ; Codon/genetics ; Containment of Biohazards/*methods ; Culture Media/chemistry/pharmacology ; Environment ; Escherichia coli/cytology/*drug effects/*genetics/metabolism ; Escherichia coli Proteins/biosynthesis/chemistry/genetics/metabolism ; Evolution, Molecular ; Gene Transfer, Horizontal/genetics ; Genes, Essential/genetics ; Genetic Code/genetics ; Genetic Engineering/methods ; Genome, Bacterial/genetics ; Microbial Viability/*drug effects/genetics ; Molecular Sequence Data ; Organisms, Genetically Modified/genetics/growth & development/metabolism ; Peptide Termination Factors/genetics ; Phenylalanine/chemistry/metabolism ; Protein Multimerization/genetics ; RNA, Transfer/genetics ; Synthetic Biology/*methods
    Print ISSN: 0028-0836
    Electronic ISSN: 1476-4687
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 8
    Publication Date: 2015-02-18
    Description: Genetically modified organisms (GMOs) are commonly used to produce valuable compounds in closed industrial systems. However, their emerging applications in open clinical or environmental settings require enhanced safety and security measures. Intrinsic biocontainment, the creation of bacterial hosts unable to survive in natural environments, remains a major unsolved biosafety problem. We developed a new biocontainment strategy containing overlapping ‘safeguards’—engineered riboregulators that tightly control expression of essential genes, and an engineered addiction module based on nucleases that cleaves the host genome—to restrict viability of Escherichia coli cells to media containing exogenously supplied synthetic small molecules. These multilayered safeguards maintain robust growth in permissive conditions, eliminate persistence and limit escape frequencies to 〈1.3 x 10 –12 . The staged approach to safeguard implementation revealed mechanisms of escape and enabled strategies to overcome them. Our safeguarding strategy is modular and employs conserved mechanisms that could be extended to clinically or industrially relevant organisms and undomesticated species.
    Print ISSN: 0305-1048
    Electronic ISSN: 1362-4962
    Topics: Biology
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 9
    Publication Date: 2010-08-16
    Print ISSN: 0027-8424
    Electronic ISSN: 1091-6490
    Topics: Biology , Medicine , Natural Sciences in General
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 10
    Publication Date: 2003-06-13
    Print ISSN: 0027-8424
    Electronic ISSN: 1091-6490
    Topics: Biology , Medicine , Natural Sciences in General
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
Close ⊗
This website uses cookies and the analysis tool Matomo. More information can be found here...