J. Beckwith

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Regulation of Escherichia coli cell envelope proteins involved in protein folding and degradation by the Cpx two-component system.

J. Pogliano, A. S. Lynch, D. Belin, 1997, Genes & development.

The Role of the Thioredoxin and Glutaredoxin Pathways in Reducing Protein Disulfide Bonds in the Escherichia coliCytoplasm*

J. Beckwith, W. Prinz, Fredrik Åslund, 1997, The Journal of Biological Chemistry.

The reducing activity of glutaredoxin 3 toward cytoplasmic substrate proteins is restricted by methionine 43.

Lennart Nilsson, Amir Porat, Jon Beckwith, 2007, Biochemistry.

How many membrane proteins are there?

J. Beckwith, D. Boyd, C. Schierle, 1998, Protein science : a publication of the Protein Society.

The lactose operon

D. Zipser, J. Beckwith, 1970 .

Localization of FtsI (PBP3) to the Septal Ring Requires Its Membrane Anchor, the Z Ring, FtsA, FtsQ, and FtsL

J. Beckwith, D. Boyd, D. S. Weiss, 1999, Journal of bacteriology.

Protein disulfide bond formation in prokaryotes.

Jon Beckwith, J. Beckwith, H. Kadokura, 2003, Annual review of biochemistry.

Snapshots of DsbA in Action: Detection of Proteins in the Process of Oxidative Folding

Thomas Zander, Jon Beckwith, J. Beckwith, 2004, Science.

The Nonconsecutive Disulfide Bond of Escherichia coli Phytase (AppA) Renders It Dependent on the Protein-disulfide Isomerase, DsbC*

J. Beckwith, D. Boyd, M. Berkmen, 2005, Journal of Biological Chemistry.

Bacterial species exhibit diversity in their mechanisms and capacity for protein disulfide bond formation

J. Beckwith, D. Boyd, M. Berkmen, 2008, Proceedings of the National Academy of Sciences.

Mechanisms of oxidative protein folding in the bacterial cell envelope.

Jon Beckwith, J. Beckwith, H. Kadokura, 2010, Antioxidants & redox signaling.

Tight regulation, modulation, and high-level expression by vectors containing the arabinose PBAD promoter

D. Belin, J. Beckwith, L. Guzmán, 1995, Journal of bacteriology.

A complex of the Escherichia coli cell division proteins FtsL, FtsB and FtsQ forms independently of its localization to the septal region

J. Beckwith, N. Buddelmeijer, 2004, Molecular microbiology.

Assembly of cell division proteins at the E. coli cell center.

J. Beckwith, N. Buddelmeijer, 2002, Current opinion in microbiology.

The Sec-dependent pathway.

J. Beckwith, 2013, Research in microbiology.

Bridge over Troubled Waters Sensing Stress by Disulfide Bond Formation

Jon Beckwith, J. Beckwith, F. Åslund, 1999, Cell.

TnphoA: a transposon probe for protein export signals.

J. Beckwith, C. Manoil, J Beckwith, 1985, Proceedings of the National Academy of Sciences of the United States of America.

The genetics of disulfide bond metabolism.

J. Beckwith, A. Rietsch, J Beckwith, 1998, Annual review of genetics.

Mutant AhpC peroxiredoxins suppress thiol-disulfide redox deficiencies and acquire deglutathionylating activity.

J. Beckwith, D. Boyd, D. Ritz, 2008, Molecular cell.

Roles of thiol-redox pathways in bacteria.

J. Beckwith, D. Ritz, J Beckwith, 2001, Annual review of microbiology.

Genetic fusions that help define a transcription termination region in Escherichia coli.

W. Reznikoff, J. Beckwith, D. Mitchell, 1976, Journal of molecular biology.

Synthesis and processing of an Escherichia coli alkaline phosphatase precursor in vitro.

J. Beckwith, H. Inouye, 1977, Proceedings of the National Academy of Sciences of the United States of America.

Transcription termination at the end of the tryptophan operon of Escherichia coli.

L. Guarente, J. Beckwith, D. Mitchell, 1977, Journal of molecular biology.

Use of gene fusions to study outer membrane protein localization in Escherichia coli.

J. Beckwith, T. Silhavy, H. Shuman, 1977, Proceedings of the National Academy of Sciences of the United States of America.

Use of Thioredoxin as a Reporter To Identify a Subset of Escherichia coli Signal Sequences That Promote Signal Recognition Particle-Dependent Translocation

M. Gerstein, Yu Xia, Michael H. Olma, 2005, Journal of bacteriology.

Mutations that alter the DNA sequence specificity of the catabolite gene activator protein of E. coli

Pascale Cossart, Richard H. Ebright, Jon Beckwith, 1984, Nature.

Cyclic Adenosine Monophosphate-Independent Mutants of the Lactose Operon of Escherichia coli

J. Beckwith, R. Arditti, T. Grodzicker, 1973, Journal of bacteriology.

Detecting Folding Intermediates of a Protein as It Passes through the Bacterial Translocation Channel

J. Beckwith, H. Kadokura, 2009, Cell.

Characterization of degP, a gene required for proteolysis in the cell envelope and essential for growth of Escherichia coli at high temperature

J. Beckwith, J Beckwith, K L Strauch, 1989, Journal of bacteriology.

Alkaline phosphatase fusions: sensors of subcellular location

J. Beckwith, J. Mekalanos, C. Manoil, 1990, Journal of bacteriology.

The use of transposon TnphoA to detect genes for cell envelope proteins subject to a common regulatory stimulus. Analysis of osmotically regulated genes in Escherichia coli.

J. Beckwith, C. Manoil, C. Gutierrez, 1987, Journal of molecular biology.

The Protein Translocation Apparatus Contributes to Determining the Topology of an Integral Membrane Protein in Escherichia coli *

J. Beckwith, W. Prinz, M. Ehrmann, 1998, The Journal of Biological Chemistry.

SecA membrane cycling at SecYEG is driven by distinct ATP binding and hydrolysis events and is regulated by SecD and SecF

J. Pogliano, J. Beckwith, W. Wickner, 1995, Cell.

Residues essential for the function of SecE, a membrane component of the Escherichia coli secretion apparatus, are located in a conserved cytoplasmic region.

J. Beckwith, C. Murphy, 1994, Proceedings of the National Academy of Sciences of the United States of America.

Overexpression of the rhodanese PspE, a single cysteine‐containing protein, restores disulphide bond formation to an Escherichia coli strain lacking DsbA

D. Vertommen, J. Beckwith, J. Collet, 2012, Molecular microbiology.

Disulfide bond formation by exported glutaredoxin indicates glutathione's presence in the E. coli periplasm

J. Beckwith, G. Georgiou, H. Kadokura, 2009, Proceedings of the National Academy of Sciences.

Conserved Role of the Linker α-Helix of the Bacterial Disulfide Isomerase DsbC in the Avoidance of Misoxidation by DsbB*

J. Beckwith, G. Georgiou, Laura Segatori, 2006, Journal of Biological Chemistry.

The genetics of protein secretion in Escherichia coli.

J. Clément, M. Hofnung, S. Emr, 1981, Methods in cell biology.

The disulfide bond isomerase DsbC is activated by an immunoglobulin‐fold thiol oxidoreductase: crystal structure of the DsbC–DsbDα complex

J. Beckwith, F. Katzen, D. Goldstone, 2002, The EMBO journal.

Role and location of the unusual redox-active cysteines in the hydrophobic domain of the transmembrane electron transporter DsbD

J. Beckwith, F. Katzen, 2003, Proceedings of the National Academy of Sciences of the United States of America.

IcsA, a polarly localized autotransporter with an atypical signal peptide, uses the Sec apparatus for secretion, although the Sec apparatus is circumferentially distributed

J. Beckwith, M. Goldberg, N. Goehring, 2003, Molecular microbiology.

Repurposing lipoic acid changes electron flow in two important metabolic pathways of Escherichia coli

J. Beckwith, G. Georgiou, D. Boyd, 2011, Proceedings of the National Academy of Sciences.

Role of Leucine Zipper Motifs in Association of the Escherichia coli Cell Division Proteins FtsL and FtsB

J. Beckwith, D. Ladant, G. Karimova, 2011, Journal of bacteriology.

Inactivation of FtsI inhibits constriction of the FtsZ cytokinetic ring and delays the assembly of FtsZ rings at potential division sites.

R. Losick, K. Pogliano, J. Pogliano, 1997, Proceedings of the National Academy of Sciences of the United States of America.

Protein export in Escherichia coli

J. Beckwith, C. Murphy, K. Johnson, 1992, Current Biology.

Deletion of the Escherichia coli crp Gene

J. Beckwith, D. Sabourin, 1975, Journal of bacteriology.

A selection for mutants that interfere with folding of Escherichia coli thioredoxin-1 in vivo.

M. L. Tasayco, A. Chaffotte, J. Beckwith, 2005, Proceedings of the National Academy of Sciences of the United States of America.

Mutants, Suppressors, and Wrinkled Colonies: Mutant Alleles of the Cell Division Gene ftsQ Point to Functional Domains in FtsQ and a Role for Domain 1C of FtsA in Divisome Assembly

J. Beckwith, I. Petrovska, D. Boyd, 2006, Journal of bacteriology.

The bonds that tie: Catalyzed disulfide bond formation

J. Beckwith, J. Bardwell, 1993, Cell.

Premature targeting of a cell division protein to midcell allows dissection of divisome assembly in Escherichia coli.

Frederico J. Gueiros-Filho, J. Beckwith, N. Goehring, 2005, Genes & development.

Escherichia colidissection of divisome assembly in Premature targeting of a cell division protein to midcell allows data

Frederico J. Gueiros-Filho, J. Beckwith, N. Goehring, 2004 .

FtsQ, FtsL and FtsI require FtsK, but not FtsN, for co‐localization with FtsZ during Escherichia coli cell division

J. Beckwith, Joseph C. Chen, J. C. Chen, 2001, Molecular microbiology.

Localization of FtsL to the Escherichia coli septal ring

J. Yarrow, J. Beckwith, Joseph C. Chen, 1999, Molecular microbiology.

Localization of the Escherichia coli cell division protein FtsI (PBP3) to the division site and cell pole

R. Losick, K. Pogliano, J. Beckwith, 1997, Molecular microbiology.

Structure of the malB region in Escherichia coli K12

L. Guarente, J. Beckwith, T. Silhavy, 1979, Molecular and General Genetics MGG.

Premature targeting of cell division proteins to midcell reveals hierarchies of protein interactions involved in divisome assembly

J. Beckwith, N. Goehring, Mark D. Gonzalez, 2006, Molecular microbiology.

Divisome under Construction: Distinct Domains of the Small Membrane Protein FtsB Are Necessary for Interaction with Multiple Cell Division Proteins

J. Beckwith, Mark D. Gonzalez, 2009, Journal of bacteriology.

Septal Localization of FtsQ, an Essential Cell Division Protein in Escherichia coli

J. Beckwith, Joseph C. Chen, J. Ghigo, 1999, Journal of bacteriology.

secE encodes an integral protein required for protein export in Escherichia coli

J. Beckwith, P. Schatz, P. Riggs, 2007 .

Molecular genetic analysis of membrane protein topology.

J. Beckwith, D. Boyd, C. Manoil, 1988, Trends in genetics : TIG.

Gene fusion analysis of membrane protein topology: a direct comparison of alkaline phosphatase and beta-lactamase fusions

J. Beckwith, W. Prinz, 1994, Journal of bacteriology.

Processing of alkaline phosphatase precursor to the mature enzyme by an Escherichia coli inner membrane preparation

J. Beckwith, P. Model, H. Inouye, 1980, Journal of bacteriology.

Positions of early nonsense and deletion mutations in lacZ

J. Beckwith, J. K. Welply, A. Fowler, 1980, Journal of bacteriology.

Sites within gene lacZ of Escherichia coli for formation of active hybrid beta-galactosidase molecules

J. Beckwith, T. Silhavy, H. Shuman, 1979, Journal of bacteriology.

Fusions of the lac operon to the transfer RNA gene tyrT of Escherichia coli.

J. Beckwith, M. Berman, 1979, Journal of molecular biology.

Position of the mutation in beta-galactosidase ochre mutant U118

J. Beckwith, A. Fowler, I. Zabin, 1978, Journal of bacteriology.

Laboratory evolution of glutathione biosynthesis reveals natural compensatory pathways.

J. Beckwith, G. Georgiou, D. Boyd, 2011, Nature chemical biology.

The Bacterial ATPase SecA Functions as a Monomer in Protein Translocation*

T. Rapoport, J. Beckwith, D. Boyd, 2005, Journal of Biological Chemistry.

Alkaline phosphatase fusions in the study of cell division genes.

J. Beckwith, M. Carson, J. Barondess, 1991, Research in microbiology.

Suppression of growth and protein secretion defects in Escherichia coli secA mutants by decreasing protein synthesis

J. Beckwith, C. Lee, 1986, Journal of bacteriology.

The product of gene secC is involved in the synthesis of exported proteins in E. coli

J. Beckwith, S. Ferro-Novick, M. Honma, 1984, Cell.

Transposition of the lac region of Escherichia coli: III. The mechanism of attachment of bacteriophage φ80 to the bacterial chromosome

J. Beckwith, E. Signer, Ethan R. Signer, 1966 .

The use of extragenic suppressors to define genes involved in protein export in Escherichia coli

J. Beckwith, C. Kumamoto, D. Oliver, 2004, Molecular and General Genetics MGG.

Genetic Fusions of the lac Operon: A New Approach to the Study of Biological Processes

L. Guarente, J. Beckwith, T. Silhavy, 1980 .

Mutants of Escherichia coli Reflect the Cold Sensitivity of Protein Export Itself Kit

J. Beckwith, Johnson Pogliano, 2002 .

Genetic analysis of protein export in Escherichia coli.

J. Beckwith, P. Schatz, 1990, Annual review of genetics.

From Protein Folding to Blood Coagulation: Menaquinone as a Metabolic Link between Bacteria and Mammals

J. Beckwith, B. Meehan, 2017 .

Regulation of a membrane component required for protein secretion in escherichia coli

J. Beckwith, D. Oliver, 1982, Cell.

Inhibition of Pseudomonas aeruginosa and Mycobacterium tuberculosis disulfide bond forming enzymes

S. Lory, J. Beckwith, E. Rubin, 2019, Molecular microbiology.

Title : Inhibition of Pseudomonas aeruginosa and Mycobacterium tuberculosis disulfide bond forming enzymes Running Title : Targeting virulence and growth of pathogenic bacteria

Tanweer, S. Lory, J. Beckwith, 2018 .

A double counter-selection system for the study of null alleles of essential genes in Escherichia coli.

J. Beckwith, E. Stewart, C. Murphy, 1995, Gene.

Folding LacZ in the Periplasm of Escherichia coli

J. Beckwith, T. Silhavy, D. Boyd, 2014, Journal of bacteriology.

Labeling of proteins with beta-galactosidase by gene fusion. Identification of a cytoplasmic membrane component of the Escherichia coli maltose transport system.

J. Beckwith, T. Silhavy, H. Shuman, 1980, The Journal of biological chemistry.

Mutagens which cause deletions in Escherichia coli.

J. Beckwith, D. Schwartz, 1969, Genetics.

Genetic Approaches for Studying Protein Localization

J. Beckwith, J. Garwin, 1982 .

The dynamics of assembly of a cytoplasmic membrane protein in Escherichia coli.

J. Beckwith, D. Boyd, C. Lee, 1992, The Journal of biological chemistry.

Positively charged amino acid residues can act as topogenic determinants in membrane proteins.

J. Beckwith, D. Boyd, 1989, Proceedings of the National Academy of Sciences of the United States of America.

Use of gene fusions to determine a partial signal sequence of alkaline phosphatase

J. Beckwith, A. Sarthy, A. Fowler, 1979, Journal of bacteriology.

Mutations at Several Loci Cause Increased Expression of Ribonucleotide Reductase in Escherichia coli

J. Beckwith, M. Feeney, N. Ke, 2012, Journal of bacteriology.

Mapping of suppressor loci in Escherichia coli.

S. Brenner, S. Brenner, J. Beckwith, 1965, Journal of molecular biology.

Inhibition of virulence-promoting disulfide bond formation enzyme DsbB is blocked by mutating residues in two distinct regions

J. Beckwith, Feras Hatahet, D. Boyd, 2017, The Journal of Biological Chemistry.

Artificial Septal Targeting of Bacillus subtilis Cell Division Proteins in Escherichia coli: an Interspecies Approach to the Study of Protein-Protein Interactions in Multiprotein Complexes

J. Beckwith, G. King, N. Goehring, 2008, Journal of bacteriology.

Artiﬁcial Septal Targeting of Bacillus subtilis Cell Division Proteins in Escherichia coli : an Interspecies Approach to the Study of Protein-Protein Interactions in Multiprotein Complexes (cid:1)

J. Beckwith, N. Goehring, Carine Robichon, 2008 .

Use of phoA fusions to study the topology of the Escherichia coli inner membrane protein leader peptidase

J. Beckwith, D. Boyd, J. L. San Millán, 1989, Journal of bacteriology.

The Disulﬁde Bond Formation Pathway Is Essential for Anaerobic Growth of Escherichia coli

J. Beckwith, D. Boyd, B. Meehan, 2017 .

The characterization of a new type of F-prime factor in Escherichia coli K12

J. Beckwith, P. Broda, J. Scaife, 1964 .

Assembly of a hetero-oligomeric membrane protein complex.

J. Beckwith, B. Traxler, 1992, Proceedings of the National Academy of Sciences of the United States of America.

Escherichia coli pleiotropic mutant that reduces amounts of several periplasmic and outer membrane proteins

B. Wanner, J. Beckwith, A. Sarthy, 1979, Journal of bacteriology.

Deletion map of the Escherichia coli structural gene for alkaline phosphatase, phoA

J. Beckwith, A. Sarthy, S. Michaelis, 1981, Journal of bacteriology.

Mutant RNA polymerase of Escherichia coli terminates transcription in strains making defective rho factor.

L. Guarente, J. Beckwith, 1978, Proceedings of the National Academy of Sciences of the United States of America.

Membrane insertion of the Escherichia coli MalF protein in cells with impaired secretion machinery.

J. Beckwith, K. McGovern, 1991, The Journal of biological chemistry.

Allelic amber and ochre suppressors.

J. Beckwith, P. Strigini, B. M. Ohlsson, 1968, Journal of molecular biology.

A DELETION ANALYSIS OF THE LAC OPERATOR REGION IN ESCHERICHIA COLI.

J. Beckwith, 1964, Journal of molecular biology.

Alkaline phosphatase synthesis in a cell-free system using DNA and RNA templates.

J. Beckwith, H. Inouye, A. Torriani, 1977, Journal of molecular biology.

RESTORATION OF OPERON ACTIVITY BY SUPPRESSORS.

J. Beckwith, Jonathan R. Beckwith, 1963, Biochimica et biophysica acta.

Catabolite Sensitive Site of the lac Operon

W. Reznikoff, Jeffrey H. Miller, J. Beckwith, 1969, Nature.

BIOLOGICAL CHLORINATION. VIII. LATE INTERMEDIATES IN THE BIOSYNTHESIS OF CALDARIOMYCIN.

J. Beckwith, L. Hager, 1963, The Journal of biological chemistry.

Secretion and processing of ribose-binding protein in Escherichia coli

J. Beckwith, J. Garwin, 1982, Journal of bacteriology.

An adenosine 3':5'-cyclic monophosphate-binding protein that acts on the transcription process.

J. Beckwith, G. Zubay, R. Arditti, 1971, Proceedings of the National Academy of Sciences of the United States of America.

bor Gene of Phage (cid:108) , Involved in Serum Resistance, Encodes a Widely Conserved Outer Membrane Lipoprotein

J. Beckwith, J. Barondess, 1995 .

Evidence for two sites in the lac promoter region.

J. Beckwith, R. Arditti, T. Grodzicker, 1972, Journal of molecular biology.

Mutations that alter the signal sequence of alkaline phosphatase in Escherichia coli

J. Beckwith, S. Michaelis, H Inouye, 1983, Journal of bacteriology.

Membrane topology and mutational analysis of Mycobacterium tuberculosis VKOR, a protein involved in disulfide bond formation and a homologue of human vitamin K epoxide reductase.

J. Beckwith, D. Boyd, R. Dutton, 2011, Antioxidants & redox signaling.

The transmembrane domain of the DnaJ-like protein DjlA is a dimerisation domain

J. Beckwith, J. Leeds, I. Holland, 2003, Molecular Genetics and Genomics.

In vitro construction and characterization of phoA-lacZ gene fusions in Escherichia coli

L. Guarente, J. Beckwith, S. Michaelis, 1983, Journal of bacteriology.

Pleiotropic mutants affecting the secretory apparatus of Escherichia coli.

J. Beckwith, C. Kumamoto, D. Oliver, 1982, Annales de microbiologie.

Gene function in prokaryotes

J. Beckwith, J. Gallant, J. Davies, 1983 .

Mechanism of activation of catabolite-sensitive genes: a positive control system.

J. Beckwith, G. Zubay, J Beckwith, 1970, Proceedings of the National Academy of Sciences of the United States of America.

Transposition of the lac region of Escherichia coli. II. On the role of thiogalactoside transacetylase in lactose metabolism.

J. Beckwith, W. Epstein, E. Signer, 1966, Journal of molecular biology.

Identification of a protein required for disulfide bond formation in vivo

J. Beckwith, J. Bardwell, K. McGovern, 1991, Cell.

Diverse Paths to Midcell: Assembly of the Bacterial Cell Division Machinery

J. Beckwith, N. Goehring, 2005, Current Biology.

Mechanism and applications of free radical cyclization

J. Beckwith, L. Athelstan, 1986 .

Coordination of the synthesis of the enzymes in the pyrimidine pathway of E. coli.

J. Beckwith, F. Jacob, A. Pardee, 1962, Journal of molecular biology.

Role for the Nonessential N Terminus of FtsN in Divisome Assembly

J. Beckwith, N. Goehring, Carine Robichon, 2006, Journal of bacteriology.

Diversity of Chemical Mechanisms in Thioredoxin Catalysis Revealed by Single-Molecule Force Spectroscopy

B. Berne, Jingyuan Li, K. Becker, 2009, Nature Structural &Molecular Biology.

Directed transposition of the arabinose operon: a technique for the isolation of specialized transducing bacteriophages for any Escherichia coli gene.

S. Gottesman, J. Beckwith, Susan Gottesman, 1969, Journal of molecular biology.

A mechanism for repressor action.

J H Miller, J. Miller, W. Reznikoff, 1969, Journal of molecular biology.

Direction of Transcription of a Regulatory Gene in E. coli

Jeffrey H. Miller, J. Beckwith, B. Muller-Hill, 1968, Nature.

SecD and SecF facilitate protein export in Escherichia coli.

J. Pogliano, J. Beckwith, J Beckwith, 1994, The EMBO journal.

Genetic and molecular characterization of the Escherichia coli secD operon and its products

K. Pogliano, J. Beckwith, J Beckwith, 1994, Journal of bacteriology.

The secD locus of E.coli codes for two membrane proteins required for protein export.

J. Beckwith, A. Jacq, K. Johnson, 1990, The EMBO journal.

secD, a new gene involved in protein export in Escherichia coli

J. Beckwith, J. Hunt, S. Benson, 1987, Journal of bacteriology.

Genetic studies on the inability of beta-galactosidase to be translocated across the Escherichia coli cytoplasmic membrane

Catherine A. Lee, J. Beckwith, P. Li, 1989, Journal of bacteriology.

Integration of Specialized Transducing Bacteriophage A cI857

J. Beckwith, S. Cohen, H. Nash, 2022 .

Transposition of the Lac region of E. coli.

J. Beckwith, W. Epstein, E. Signer, 1966, Cold Spring Harbor symposia on quantitative biology.

Transposition of the lac region of Escherichia coli. I. Inversion of the lac operon and transduction of lac by phi80.

J. Beckwith, E. Signer, J R Beckwith, 1966, Journal of molecular biology.

The promoter-operator region of the lac operon of Escherichia coli.

J. Miller, J. Beckwith, J. Scaife, 1968, Journal of molecular biology.

New Controlling Element in the Lac Operon of E. coli

Jeffrey H. Miller, J. Beckwith, KARIN IPPEN, 1968, Nature.

The nature of mutants in the lac promoter region.

J. Beckwith, J. Scaife, R. Arditti, 1968, Journal of molecular biology.

Nonsense mutants and polarity in the lac operon of Escherichia coli.

D. Zipser, S. Brenner, J. Beckwith, 1965, Journal of molecular biology.

Isolation of Pure lac Operon DNA*

J. Beckwith, L. Machattie, G. Ihler, 1969, Nature.

Evidence for specificity at an early step in protein export in Escherichia coli

J. Beckwith, C. Kumamoto, 1985, Journal of bacteriology.

The plug domain of the SecY protein stabilizes the closed state of the translocation channel and maintains a membrane seal.

Sol Schulman, Weikai Li, Jon Beckwith, 2007, Molecular cell.

Isolation and characterization of mutants of Escherichia coli K12 affected in protein localization.

J. Beckwith, T. Silhavy, 1983, Methods in enzymology.

Identification of a new gene (secA) and gene product involved in the secretion of envelope proteins in Escherichia coli

J. Beckwith, D. Oliver, 1982, Journal of bacteriology.

Fifty years fused to lac.

J. Beckwith, 2013, Annual review of microbiology.

In Vivo Analyses of Interactions between SecE and SecY, Core Components of the Escherichia coli Protein Translocation Machinery*

J. Beckwith, M. Pohlschröder, Christopher Murphy, 1996, The Journal of Biological Chemistry.

Characterization of cold-sensitive secY mutants of Escherichia coli

J. Beckwith, C. Ueguchi, K. Ito, 1990, Journal of bacteriology.

Does secA mediate coupling between secretion and translation in Escherichia coli?

J. Beckwith, C. Kumamoto, K. L. Strauch, 1986, Journal of bacteriology.

Cotranslational and posttranslational protein translocation in prokaryotic systems.

J. Beckwith, C. Lee, 1986, Annual review of cell biology.

Genetic studies on protein export in bacteria.

J. Beckwith, S. Ferro-Novick, 1986, Current topics in microbiology and immunology.

Escherichia coli 6S RNA is not essential for growth or protein secretion

J. Beckwith, M. Fournier, C. Lee, 1985, Journal of bacteriology.

Signal sequence mutations disrupt feedback between secretion of an exported protein and its synthesis in E. coli

Carol A. Kumamoto, Jon Beckwith, J. Beckwith, 1984, Nature.

Mechanism of incorporation of cell envelope proteins in Escherichia coli.

J. Beckwith, J Beckwith, S Michaelis, 1982, Annual review of microbiology.

E. coli mutant pleiotropically defective in the export of secreted proteins

J. Beckwith, D. Oliver, 1981, Cell.

The secE gene encodes an integral membrane protein required for protein export in Escherichia coli.

J. Beckwith, P. Schatz, P. Riggs, 1989, Genes & development.

A mutation affecting the regulation of a secA-lacZ fusion defines a new sec gene.

J. Beckwith, A. Derman, J Beckwith, 1988, Genetics.

Effects of signal sequence mutations on the kinetics of alkaline phosphatase export to the periplasm in Escherichia coli

J. Beckwith, J. Hunt, S. Michaelis, 1986, Journal of bacteriology.

Mutations in a new gene, secB, cause defective protein localization in Escherichia coli

J. Beckwith, C. Kumamoto, 1983, Journal of bacteriology.

Genetic analysis of protein export in Escherichia coli.

J. Beckwith, T. Silhavy, J Beckwith, 1983, Methods in enzymology.

Disulfide bond formation in prokaryotes

J. Beckwith, D. Boyd, Cristina Landeta, 2018, Nature Microbiology.

A genetic approach to analyzing membrane protein topology.

J. Beckwith, C. Manoil, J Beckwith, 1986, Science.

One of three transmembrane stretches is sufficient for the functioning of the SecE protein, a membrane component of the E. coli secretion machinery.

J. Beckwith, T. Silhavy, P. Schatz, 1991, The EMBO journal.

Regulation of the Lac Operon

Jon Beckwith, J. Beckwith, 1967 .

Escherichia coli alkaline phosphatase fails to acquire disulfide bonds when retained in the cytoplasm

J. Beckwith, A. Derman, J Beckwith, 1991, Journal of bacteriology.

Escherichia coli alkaline phosphatase localized to the cytoplasm slowly acquires enzymatic activity in cells whose growth has been suspended: a caution for gene fusion studies

J. Beckwith, A. Derman, 1995, Journal of bacteriology.

Mutations that allow disulfide bond formation in the cytoplasm of Escherichia coli.

D. Belin, J. Beckwith, W. Prinz, 1993, Science.

Use of gene fusion to study secretion of maltose-binding protein into Escherichia coli periplasm

J. Beckwith, T. Silhavy, P. Bassford, 1979, Journal of bacteriology.

Importance of Redox Potential for the in VivoFunction of the Cytoplasmic Disulfide Reductant Thioredoxin fromEscherichia coli *

R. Glockshuber, J. Beckwith, Fredrik Åslund, 1999, The Journal of Biological Chemistry.

Uses of lac fusions for the study of biological problems.

J. Beckwith, T. Silhavy, Thomas J. SILHAVYl, 1985, Microbiological reviews.

Production of functional single-chain Fv antibodies in the cytoplasm of Escherichia coli.

V. de Lorenzo, J. Beckwith, D. Ritz, 2002, Journal of molecular biology.

Interactions of glutaredoxins, ribonucleotide reductase, and components of the DNA replication system of Escherichia coli.

Amir Porat, Jon Beckwith, J. Beckwith, 2004, Proceedings of the National Academy of Sciences of the United States of America.

Genetic selection for and molecular dynamic modeling of a protein transmembrane domain multimerization motif from a random Escherichia coli genomic library.

D. Engelman, J. Beckwith, D. Boyd, 2001, Journal of molecular biology.

An in vivo pathway for disulfide bond isomerization in Escherichia coli.

D. Belin, J. Beckwith, A. Rietsch, 1996, Proceedings of the National Academy of Sciences of the United States of America.

Protein Translocation in the Three Domains of Life: Variations on a Theme

Jon Beckwith, E. Hartmann, J. Beckwith, 1997, Cell.

The role of charged amino acids in the localization of secreted and membrane proteins

Jon Beckwith, J. Beckwith, D. Boyd, 1990, Cell.

bor gene of phage lambda, involved in serum resistance, encodes a widely conserved outer membrane lipoprotein

J. Beckwith, J. Barondess, 1995, Journal of bacteriology.

In vitro Transcription of the lac Operon Genes

J. Beckwith, G. Zubay, R. Arditti, 1970 .

Transmembrane Electron Transfer by the Membrane Protein DsbD Occurs via a Disulfide Bond Cascade

J. Beckwith, F. Katzen, 2000, Cell.

Ribonucleotide reductases: influence of environment on synthesis and activity.

J. Beckwith, S. Gon, Stéphanie Gon, 2006, Antioxidants & redox signaling.

Genetic fusions defining trp and lac operon regulatory elements.

W. Reznikoff, J. Beckwith, D. Mitchell, 1975, Journal of molecular biology.

Fusions of the lac and trp regions of escherichia coli: covalently fused messenger RNA.

W. Reznikoff, J. Beckwith, D. Morse, 1971, Journal of molecular biology.

Transposition of the lac Region to the gal Region of the Escherichia coli Chromosome: Isolation of λlac Transducing Bacteriophages

J. Shapiro, J. Beckwith, K. Ippen, 1971, Journal of bacteriology.

Identification of the Thioredoxin Partner of Vitamin K Epoxide Reductase in Mycobacterial Disulfide Bond Formation

J. Beckwith, D. Boyd, Xiao-yun Wang, 2018, Journal of bacteriology.

The DsbA Signal Sequence Directs Efficient, Cotranslational Export of Passenger Proteins to the Escherichia coli Periplasm via the Signal Recognition Particle Pathway

J. Beckwith, D. Boyd, C. Schierle, 2003, Journal of bacteriology.

Genetic Screen Yields Mutations in Genes Encoding All Known Components of the Escherichia coli Signal Recognition Particle Pathway

Jon Beckwith, J. Beckwith, H. Tian, 2002, Journal of bacteriology.

A mutant hunt for defects in membrane protein assembly yields mutations affecting the bacterial signal recognition particle and Sec machinery.

J. Beckwith, D. Boyd, H. Tian, 2000, Proceedings of the National Academy of Sciences of the United States of America.

On the Functional Interchangeability, Oxidant versus Reductant, of Members of the Thioredoxin Superfamily

J. Beckwith, L. Debarbieux, 2000, Journal of bacteriology.

The reductive enzyme thioredoxin 1 acts as an oxidant when it is exported to the Escherichia coli periplasm.

J. Beckwith, L. Debarbieux, Laurent Debarbieux, 1998, Proceedings of the National Academy of Sciences of the United States of America.

Biotinylation in vivo as a sensitive indicator of protein secretion and membrane protein insertion

J. Beckwith, J. Cronan, G. Jander, 1996, Journal of bacteriology.

A pathway for disulfide bond formation in vivo.

D. Belin, J. Beckwith, J. Bardwell, 1993, Proceedings of the National Academy of Sciences of the United States of America.

Disulfide bond formation in the Escherichia coli cytoplasm: an in vivo role reversal for the thioredoxins

J. Beckwith, E. Stewart, F. Åslund, 1998, The EMBO journal.

Efficient folding of proteins with multiple disulfide bonds in the Escherichia coli cytoplasm.

Paul H. Bessette, J. Beckwith, G. Georgiou, 1999, Proceedings of the National Academy of Sciences of the United States of America.

Ochre mutants, a new class of suppressible nonsense mutants

S. Brenner, J. Beckwith, 1965 .

Disulfide Rearrangement Triggered by Translocon Assembly Controls Lipopolysaccharide Export

J. Beckwith, D. Boyd, D. Kahne, 2012, Science.

NMR solution structure of the integral membrane enzyme DsbB: functional insights into DsbB-catalyzed disulfide bond formation.

J. Beckwith, T. Cierpicki, Yunpeng Zhou, 2008, Molecular cell.

Genetic Suppressors and Recovery of Repressed Biochemical Memory

J. Beckwith, 2009, Journal of Biological Chemistry.

The operon as paradigm: normal science and the beginning of biological complexity.

J. Beckwith, 2011, Journal of molecular biology.

Gene expression in bacteria and some concerns about the misuse of science.

J. Beckwith, J R Beckwith, 1970, Bacteriological reviews.

The Role of the Promoter Site in Gene Expression

Jeffrey H. Miller, J. Beckwith, J. Scaife, 1968 .

Genetic determination of constitutive enzyme levels.

J. Beckwith, A. Pardee, 1962, Biochimica et biophysica acta.

D-ribose metabolism in Escherichia coli K-12: genetics, regulation, and transport

S. Emr, J. Beckwith, T. Silhavy, 1984, Journal of bacteriology.

Mutations in a new chromosomal gene of Escherichia coli K-12, pcnB, reduce plasmid copy number of pBR322 and its derivatives

J. Beckwith, J. Lopilato, Scott R. Bortner, 1986, Molecular and General Genetics MGG.

An Escherichia coli mutation preventing degradation of abnormal periplasmic proteins.

J. Beckwith, K. L. Strauch, 1988, Proceedings of the National Academy of Sciences of the United States of America.

In vivo requirement for glutaredoxins and thioredoxins in the reduction of the ribonucleotide reductases of Escherichia coli.

J. Beckwith, M. Faulkner, S. Gon, 2006, Antioxidants & redox signaling.

Multiple Interaction Domains in FtsL, a Protein Component of the Widely Conserved Bacterial FtsLBQ Cell Division Complex

J. Beckwith, D. Boyd, Mark D. Gonzalez, 2010, Journal of bacteriology.

Mutational alteration of the maximal level of Lac operon expression.

J. Beckwith, J. Scaife, 1966, Cold Spring Harbor symposia on quantitative biology.

The FtsQ protein of Escherichia coli: membrane topology, abundance, and cell division phenotypes due to overproduction and insertion mutations

J. Beckwith, M. Carson, J. Barondess, 1991, Journal of bacteriology.

Genetic Characterization of Mutations Which Affect Catabolite-Sensitive Operons in Escherichia coli, Including Deletions of the Gene for Adenyl Cyclase

J. Beckwith, L. Soll, E. Brickman, 1973, Journal of bacteriology.

Diversity of chemical mechanisms in thioredoxin catalysis revealed by single-molecule force spectroscopy

B. Berne, Jingyuan Li, K. Becker, 2009, Nature Structural &Molecular Biology.

The essential cell division protein FtsN contains a critical disulfide bond in a non‐essential domain

J. Beckwith, D. Boyd, Cristina Landeta, 2017, Molecular microbiology.

The nucleotide sequence of the gene for malF protein, an inner membrane component of the maltose transport system of Escherichia coli. Repeated DNA sequences are found in the malE-malF intercistronic region.

J. Beckwith, S. Froshauer, 1984, The Journal of biological chemistry.

Use of TnphoA to detect genes for exported proteins in Escherichia coli: identification of the plasmid-encoded gene for a periplasmic acid phosphatase

J. Beckwith, C. Manoil, P. Boquet, 1987, Journal of bacteriology.

A New Family of Membrane Electron Transporters and Its Substrates, Including a New Cell Envelope Peroxiredoxin, Reveal a Broadened Reductive Capacity of the Oxidative Bacterial Cell Envelope

J. Beckwith, J. Collet, R. Dutton, 2012, mBio.

Genetic Characterization of a Stable F ' lac Plasmid '

J. Beckwith, B. Bachmann, J. Calvo, 2022 .

Aeropyrum pernix membrane topology of protein VKOR promotes protein disulfide bond formation in two subcellular compartments.

J. Beckwith, D. Boyd, M. Berkmen, 2017, Microbiology.

Structure of a bacterial homolog of vitamin K epoxide reductase

T. Rapoport, J. Beckwith, D. Boyd, 2010, Nature.

The prokaryotic enzyme DsbB may share key structural features with eukaryotic disulfide bond forming oxidoreductases

C. Sevier, C. Kaiser, J. Beckwith, 2005, Protein science : a publication of the Protein Society.

The expanding world of oxidative protein folding

J. Beckwith, H. Kadokura, 2001, Nature Cell Biology.

Electron Avenue Pathways of Disulfide Bond Formation and Isomerization

Jon Beckwith, J. Beckwith, L. Debarbieux, 1999, Cell.

Reduction of the periplasmic disulfide bond isomerase, DsbC, occurs by passage of electrons from cytoplasmic thioredoxin

Paul H. Bessette, J. Beckwith, G. Georgiou, 1997, Journal of bacteriology.

Regulation of the OxyR transcription factor by hydrogen peroxide and the cellular thiol-disulfide status.

G. Storz, J. Beckwith, M. Zheng, 1999, Proceedings of the National Academy of Sciences of the United States of America.

Disulfide bond formation in prokaryotes: history, diversity and design.

J. Beckwith, Feras Hatahet, D. Boyd, 2014, Biochimica et biophysica acta.

Use of gene fusions to isolate promoter mutants in the transfer RNA gene tyrT of Escherichia coli.

J. Beckwith, M. Berman, 1979, Journal of molecular biology.

Conversion of beta-galactosidase to a membrane-bound state by gene fusion.

J. Beckwith, T. Silhavy, M. Casadaban, 1976, Proceedings of the National Academy of Sciences of the United States of America.

FtsL, an Essential Cytoplasmic Membrane Protein Involved in Cell Division in Escherichia coli

J. Beckwith, L. Guzmán, J. Barondess, 1992, Journal of bacteriology.

Towards Single-Copy Gene Expression Systems Making Gene Cloning Physiologically Relevant: Lambda InCh, a Simple Escherichia coli Plasmid-Chromosome Shuttle System

J. Beckwith, D. Boyd, Joseph C. Chen, 2000, Journal of bacteriology.

Role of glutamic acid-181 in DNA-sequence recognition by the catabolite gene activator protein (CAP) of Escherichia coli: altered DNA-sequence-recognition properties of [Val181]CAP and [Leu181]CAP.

T. Kunkel, R. Ebright, H. Buc, 1987, Proceedings of the National Academy of Sciences of the United States of America.

A genetic approach to characterizing complex promoters in E. coli

J. Beckwith, 1981, Cell.

Conversion of a Peroxiredoxin into a Disulfide Reductase by a Triplet Repeat Expansion

J. Beckwith, D. Ritz, L. Poole, 2001, Science.

Mutations which alter the function of the signal sequence of the maltose binding protein of Escherichia coli

Audree V. Fowler, Jon Beckwith, M. Hofnung, 1980, Nature.

Molecular basis of DNA sequence recognition by the catabolite gene activator protein: detailed inferences from three mutations that alter DNA sequence specificity.

R. Ebright, P. Cossart, J. Beckwith, 1984, Proceedings of the National Academy of Sciences of the United States of America.

Deletions of distal sequence affect termination of transcription at the end of the tryptophan operon in E. coli

L. Guarente, J. Beckwith, T. Platt, 1980, Cell.

A gene fusion method for assaying interactions of protein transmembrane segments in vivo.

J. Beckwith, J. Leeds, 2000, Methods in enzymology.

Lambda repressor N-terminal DNA-binding domain as an assay for protein transmembrane segment interactions in vivo.

J. Beckwith, J. Leeds, 1998, Journal of molecular biology.

Targeting of signal sequenceless proteins for export in Escherichia coli with altered protein translocase.

J. Beckwith, W. Prinz, M. Ehrmann, 1996, The EMBO journal.

Functions of thiol-disulfide oxidoreductases in E. coli: redox myths, realities, and practicalities.

J. Beckwith, R. Ortenberg, 2003, Antioxidants & redox signaling.

Redox state of cytoplasmic thioredoxin.

J. Beckwith, D. Ritz, 2002, Methods in enzymology.

Evolutionary domain fusion expanded the substrate specificity of the transmembrane electron transporter DsbD

Jon Beckwith, F. Daldal, J. Beckwith, 2002, The EMBO journal.

A bacterial virulence determinant encoded by lysogenic coliphage λ

Jon Beckwith, J. Beckwith, Barondess Jj, 1990 .

In vivo oxidative protein folding can be facilitated by oxidation–reduction cycling

J. Beckwith, D. Boyd, M. Berkmen, 2010, Molecular microbiology.

Use of Thioredoxin as a Reporter To Identify a Subset of Escherichia coli Signal Sequences That Promote Signal Recognition Particle-Dependent Translocation

M. Gerstein, Yu Xia, Michael H. Olma, 2005, Journal of Bacteriology.

The Thioredoxin Superfamily: Redundancy, Specificity, and Gray-Area Genomics

Jon Beckwith, J. Beckwith, Fredrik Åslund, 1999, Journal of bacteriology.

The catabolite gene activator protein (CAP) is not required for indole-3-acetic acid to activate transcription of the araBAD operon of Escherichia coli K-12

R. Ebright, J. Beckwith, 2004, Molecular and General Genetics MGG.

The all purpose gene fusion.

J. Beckwith, 2000, Methods in enzymology.

Genetic analysis of the membrane insertion and topology of MalF, a cytoplasmic membrane protein of Escherichia coli.

J. Beckwith, D. Boyd, J Beckwith, 1988, Journal of molecular biology.

Role of the mature protein sequence of maltose-binding protein in its secretion across the E. coli cytoplasmic membrane

Koreaki Ito, J. Beckwith, 1981, Cell.

Use of gene fusions to determine the orientation of gene phoA on the Escherichia coli chromosome

J. Beckwith, A. Sarthy, S. Michaelis, 1981, Journal of bacteriology.

Escherichia coli mutants accumulating the precursor of a secreted protein in the cytoplasm

J. Beckwith, P. Bassford, 1979, Nature.

Escherichia coli K-12 mutants that allow transport of maltose via the beta-galactoside transport system

J. Beckwith, H. Shuman, 1979, Journal of bacteriology.

Analysis of genetic regulatory mechanisms.

J. Beckwith, P. Rossow, 1974, Annual review of genetics.

Fusions of the lac and trp Regions of the Escherichia coli Chromosome

W. Reznikoff, J. Beckwith, E. Signer, 1970, Journal of bacteriology.

Determinants of membrane protein topology.

J. Beckwith, D. Boyd, C. Manoil, 1987, Proceedings of the National Academy of Sciences of the United States of America.

Evidence that the pathway of disulfide bond formation in Escherichia coli involves interactions between the cysteines of DsbB and DsbA.

J. Beckwith, C. Guilhot, N. Martin, 1995, Proceedings of the National Academy of Sciences of the United States of America.

Strategies for finding mutants.

J. Beckwith, 1991, Methods in enzymology.

The Mechanism of Activation of Catabolite-Sensitive Genes

J. Beckwith, G. Zubay, D. Schwartz, 1970 .

Two cysteines in each periplasmic domain of the membrane protein DsbB are required for its function in protein disulfide bond formation.

J. Beckwith, N. Martin, G. Jander, 1994, The EMBO journal.

Genetic evidence that the operator locus is distinct from the the z gene in the lac operon of Escherichia coli.

W. Reznikoff, J. Beckwith, 1969, Journal of molecular biology.

Functional activity of eukaryotic signal sequences in Escherichia coli: the ovalbumin family of serine protease inhibitors.

D. Belin, J. Beckwith, L. Guzmán, 2004, Journal of molecular biology.

A signal sequence is not required for protein export in prlA mutants of Escherichia coli.

J. Beckwith, A. Derman, P. Bassford, 1993, The EMBO journal.

Altered Escherichia coli membrane protein assembly machinery allows proper membrane assembly of eukaryotic protein vitamin K epoxide reductase

Yongxin Zhao, R. Campbell, J. Beckwith, 2015, Proceedings of the National Academy of Sciences.

Inhibition of bacterial disulfide bond formation by the anticoagulant warfarin

J. Beckwith, E. Rubin, D. Boyd, 2009, Proceedings of the National Academy of Sciences.

Rapid β-lactam-induced lysis requires successful assembly of the cell division machinery

R. Kishony, J. Beckwith, D. Kahne, 2009, Proceedings of the National Academy of Sciences.

A novel regulatory mechanism couples deoxyribonucleotide synthesis and DNA replication in Escherichia coli

Jon Beckwith, K. Skarstad, J. Beckwith, 2006, The EMBO journal.

The primary pathway of protein export in E. coli

Koreaki Ito, J. Beckwith, C. Kumamoto, 1991, Cell.

Cloning and restriction mapping of the alkaline phosphatase structural gene (phoA) of Escherichia coli and generation of deletion mutants in vitro

J. Beckwith, H. Inouye, A. Wright, 1981, Journal of bacteriology.

Structure and multistate function of the transmembrane electron transporter CcdA

J. Chou, J. Beckwith, J. Collet, 2015, Nature Structural &Molecular Biology.

Two Snapshots of Electron Transport across the Membrane

J. Beckwith, Seung-Hyun Cho, 2009, Journal of Biological Chemistry.

Redox‐active cysteines of a membrane electron transporter DsbD show dual compartment accessibility

J. Beckwith, Seung-Hyun Cho, Jiqing Ye, 2007, The EMBO journal.

The unusual transmembrane electron transporter DsbD and its homologues: a bacterial family of disulfide reductases.

J. Beckwith, Seung-Hyun Cho, Amir Porat, 2004, Research in microbiology.

Six conserved cysteines of the membrane protein DsbD are required for the transfer of electrons from the cytoplasm to the periplasm of Escherichia coli

J. Beckwith, E. Stewart, F. Katzen, 1999, The EMBO journal.

Decoding signals for membrane protein assembly using alkaline phosphatase fusions.

J. Beckwith, M. Ehrmann, J Beckwith, 1991, The EMBO journal.

Genetic analysis of membrane protein topology by a sandwich gene fusion approach.

J. Beckwith, M. Ehrmann, D. Boyd, 1990, Proceedings of the National Academy of Sciences of the United States of America.

Protein localization in E. coli: Is there a common step in the secretion of periplasmic and outer-membrane proteins?

Koreaki Ito, J. Beckwith, P. Bassford, 1981, Cell.

Alteration of the amino terminus of the mature sequence of a periplasmic protein can severely affect protein export in Escherichia coli.

J. Beckwith, P. Li, H. Inouye, 1988, Proceedings of the National Academy of Sciences of the United States of America.

Biological chlorination. II. The biosynthesis of 5-chlorolevulinic acid.

J. Beckwith, L. Hager, P. Shaw, 1959, The Journal of biological chemistry.

Evidence from Artificial Septal Targeting and Site-Directed Mutagenesis that Residues in the Extracytoplasmic β Domain of DivIB Mediate Its Interaction with the Divisomal Transpeptidase PBP 2B

J. Beckwith, G. King, S. Rowland, 2010, Journal of bacteriology.

The Cs sec mutants of Escherichia coli reflect the cold sensitivity of protein export itself.

K. Pogliano, J. Beckwith, 1993, Genetics.

Determinants of activity in glutaredoxins: an in vitro evolved Grx1-like variant of Escherichia coli Grx3.

P. Güntert, K. Berndt, J. Beckwith, 2010, The Biochemical journal.

BIOLOGICAL CHLORINATION. VII. STUDIES ON THE BIOSYNTHESIS OF CALDARIOMYCIN.

J. Beckwith, L. Hager, R. Clark, 1963, Journal of Biological Chemistry.

Domain-swapping analysis of FtsI, FtsL, and FtsQ, bitopic membrane proteins essential for cell division in Escherichia coli

J. Beckwith, L. Guzmán, D. Weiss, 1997, Journal of bacteriology.

Thioredoxin 2 Is Involved in the Oxidative Stress Response inEscherichia coli *

G. Storz, J. Beckwith, Fredrik Åslund, 2000, The Journal of Biological Chemistry.

What Lies Beyond Uranus?: Preconceptions, Ignorance, Serendipity and Suppressors in the Search for Biology's Secrets

J. Beckwith, 2007, Genetics.

Functional plasticity of a peroxidase allows evolution of diverse disulfide-reducing pathways

J. Beckwith, M. Faulkner, George R. Georgiou, 2008, Proceedings of the National Academy of Sciences.

lac: The Genetic System

Jon Beckwith, J. Beckwith, 1980 .

Analysis of ftsQ Mutant Alleles in Escherichia coli: Complementation, Septal Localization, and Recruitment of Downstream Cell Division Proteins

J. Beckwith, Joseph C. Chen, M. Minev, 2002, Journal of bacteriology.

Disulfide bond formation in prokaryotes

J. Beckwith, D. Boyd, Cristina Landeta, 2018, Nature Microbiology.

Contribution of the FtsQ Transmembrane Segment to Localization to the Cell Division Site

J. Beckwith, G. Koningstein, T. den Blaauwen, 2007, Journal of bacteriology.

Four cysteines of the membrane protein DsbB act in concert to oxidize its substrate DsbA

J. Beckwith, H. Kadokura, 2002, The EMBO journal.

Roles of a conserved arginine residue of DsbB in linking protein disulfide-bond-formation pathway to the respiratory chain of Escherichia coli.

J. Beckwith, M. Bader, H. Kadokura, 2000, Proceedings of the National Academy of Sciences of the United States of America.

Proper insertion of a complex membrane protein in the absence of its amino-terminal export signal.

J. Beckwith, M. Ehrmann, 1991, The Journal of biological chemistry.

Compounds targeting disulfide bond forming enzyme DsbB of Gram-negative bacteria

J. Beckwith, Alissa Myrick, E. Rubin, 2015, Nature chemical biology.

DsbC activation by the N-terminal domain of DsbD

J. Beckwith, M. Bader, F. Katzen, 2001, Proceedings of the National Academy of Sciences of the United States of America.

Chapter 5 Steps in the assembly of a cytoplasmic membrane protein: the MalF component of the maltose transport complex

J. Beckwith, B. Traxler, 1992 .

Signal sequence of alkaline phosphatase of Escherichia coli

J. Beckwith, W. Barnes, H Inouye, 1982, Journal of bacteriology.

Analysis of the topology of a membrane protein by using a minimum number of alkaline phosphatase fusions

J. Beckwith, D. Boyd, J Beckwith, 1993, Journal of bacteriology.

YgbQ, a cell division protein in Escherichia coli and Vibrio cholerae, localizes in codependent fashion with FtsL to the division site

J. Beckwith, J. Mekalanos, D. Boyd, 2002, Proceedings of the National Academy of Sciences of the United States of America.

Cell Division in Escherichia coli: Role of FtsL Domains in Septal Localization, Function, and Oligomerization

J. Beckwith, J. Ghigo, 2000, Journal of bacteriology.

The topological analysis of integral cytoplasmic membrane proteins

Jon Beckwith, J. Beckwith, D. Boyd, 1993, The Journal of Membrane Biology.

PBAD promoter. arabinose expression by vectors containing the Tight regulation, modulation, and high-level

D. Belin, J. Beckwith, M. Carson, 2013 .

Regulation of the lac operon. Recent studies on the regulation of lactose metabolism in Escherichia coli support the operon model.

J. Beckwith, J R Beckwith, 1967, Science.

Amino acid residues important for folding of thioredoxin are revealed only by study of the physiologically relevant reduced form of the protein.

A. Chaffotte, J. Beckwith, D. Huber, 2010, Biochemistry.

Crystal Structure of an Unusual Thioredoxin Protein with a Zinc Finger Domain*

T. Rapoport, J. Beckwith, Seung-Hyun Cho, 2007, Journal of Biological Chemistry.

On the Functional Interchangeability, Oxidant versus Reductant, of Members of the Thioredoxin Superfamily

J. Beckwith, L. Debarbieux, 2000, Journal of bacteriology.

Mutational Alterations of the Key cis Proline Residue That Cause Accumulation of Enzymatic Reaction Intermediates of DsbA, a Member of the Thioredoxin Superfamily

J. Beckwith, H. Kadokura, Lorenzo L. Nichols, 2005, Journal of bacteriology.

Role of Leucine Zipper Motifs in Association of the Escherichia coli Cell Division Proteins FtsL and FtsB

J. Beckwith, D. Ladant, G. Karimova, 2011, Journal of bacteriology.

Research Article 16: Mutants Missing a Factor Necessary for the Expression of Catabolite-Sensitive Operons in E. coli

J. Beckwith, D. Schwartz, 1970 .

THE CHROMOSOMAL LOCATION OF THE STRUCTURAL GENE FOR OROTIDYLIC ACID PYROPHOSPHORYLASE IN ESCHERICHIA COLI.

J. Beckwith, F. Jacob, A. Pardee, 1964, Journal of molecular biology.

The Implications of Sociobiology

S. Chorover, T. Judd, J. Beckwith, 1976, Science.