about
Precise manipulation of chromosomes in vivo enables genome-wide codon replacementTranslation system engineering in Escherichia coli enhances non-canonical amino acid incorporation into proteins.Cell-free protein synthesis with prokaryotic combined transcription-translation.Evolution of translation initiation sequences using in vitro yeast ribosome display.Depletion of Shine-Dalgarno Sequences within Bacterial Coding Regions Is Expression Dependent.Leveraging genome-wide datasets to quantify the functional role of the anti-Shine-Dalgarno sequence in regulating translation efficiency.NullSeq: A Tool for Generating Random Coding Sequences with Desired Amino Acid and GC Contents.A cell-free platform for rapid synthesis and testing of active oligosaccharyltransferases.Editorial overview: Synthetic biology: Frontiers in synthetic biology.Controlling cell-free metabolism through physiochemical perturbations.A Pipeline for Studying and Engineering Single-Subunit Oligosaccharyltransferases.Repurposing ribosomes for synthetic biology.Cogenerating Synthetic Parts toward a Self-Replicating System.A novel framework for evaluating the performance of codon usage bias metrics.Development of a CHO-Based Cell-Free Platform for Synthesis of Active Monoclonal Antibodies.How many human proteoforms are there?Incorporation of Nonproteinogenic Amino Acids in Class I and II Lantibiotics.Establishing a high yielding streptomyces-based cell-free protein synthesis system.Cell-free protein synthesis from genomically recoded bacteria enables multisite incorporation of noncanonical amino acids.Single-pot glycoprotein biosynthesis using a cell-free transcription-translation system enriched with glycosylation machinery.Establishing a High-Yielding Cell-Free Protein Synthesis Platform Derived from Vibrio natriegensExposed to Sublethal Levels of Hydrogen Peroxide Mounts a Complex Transcriptional ResponseHigh-throughput optimization cycle of a cell-free ribosome assembly and protein synthesis systemAuthor Correction: Single-pot glycoprotein biosynthesis using a cell-free transcription-translation system enriched with glycosylation machineryBioBits™ Bright: A fluorescent synthetic biology education kitBioBits™ Explorer: A modular synthetic biology education kitAssembly and functionality of the ribosome with tethered subunitsCell-free biosynthesis of limonene using enzyme-enriched lysatesHigh-throughput mapping of CoA metabolites by SAMDI-MS to optimize the cell-free biosynthesis of HMG-CoA.Design of glycosylation sites by rapid synthesis and analysis of glycosyltransferasesMutational characterization and mapping of the 70S ribosome active siteDesign and Optimization of a Cell-Free Atrazine BiosensorIn vitro ribosome synthesis and evolution through ribosome displaySequential Glycosylation of Proteins with Substrate-Specific N-GlycosyltransferasesPoint-of-care biomarker quantification enabled by sample-specific calibrationTotal in vitro biosynthesis of the nonribosomal macrolactone peptide valinomycinDeconstructing Cell-Free Extract Preparation for in Vitro Activation of Transcriptional Genetic CircuitryExpanding the limits of the second genetic code with ribozymesA Highly Productive, One-Pot Cell-Free Protein Synthesis Platform Based on Genomically Recoded Escherichia coliOrganism Engineering for the Bioproduction of the Triaminotrinitrobenzene (TATB) Precursor Phloroglucinol (PG)
P50
Q28243372-FB051E72-B537-4446-9016-AD5D5AC43B41Q30396587-DDC16CDB-9BA5-4AC7-B436-0B1F1A696BEBQ31097951-CE2F5D87-ED4A-409F-8959-06ABBCD185C0Q35891688-06451A4E-E3A9-425B-9D84-A54F3F54C266Q37401494-FA8340D6-EECB-4098-A126-75A138C0FF9BQ37637098-75BFFCF3-5416-4B57-B925-BD5F982165DAQ38434954-45B5FAF7-81FD-4A45-ACE3-36BAAB7B5B76Q47311227-A8772273-290D-4D8B-80ED-4D115B9E3DBEQ47331493-175F45CC-CDC1-4DB8-B6C7-FC64793E3012Q47332629-867A0F53-29DF-4B16-931D-18934088427CQ47650270-CAFA98F5-382A-4B37-9743-5E53A41EA8E1Q47719147-5C4027B2-2D02-4AEE-8283-D99C155CABA2Q48044180-1F33DD40-8D59-4725-91BA-995FA34D936CQ48130946-5AE2BF18-FD33-4C43-866B-B6D8F3B7B395Q48351765-38EDB3DB-B829-487D-A01E-ED5BFD2759E7Q50001631-FEB8502B-E47E-4A2D-B51C-9791A2FD6759Q50033661-EF557CAC-2342-42D3-BC65-7375D42835DEQ50210058-044DF351-099B-488A-8F4C-2C35F69D5FFCQ55057298-1F7FA191-3736-4BC5-8C90-92DC3370EDC0Q55689952-DF460C58-0B21-46D2-A5AC-FC5BA6169D1CQ57275366-FA4ED221-79A4-48F3-8798-FB00AD56288DQ57485144-D3E48451-0CE1-4C21-B598-0D88FBF54C56Q57789389-95F1882D-EE0A-4F3D-AC6C-30F198B15309Q58737163-1D67357D-52C9-47DD-B1F3-39FBC8BDBE42Q63246717-51960B28-6FB5-43CF-8BF9-B86F273207F8Q63246719-4C85C2B4-602F-4666-B99A-D48CE7B7E12BQ64106177-8407E5E5-B0E3-4063-A6FF-4E0B8E5AEAF8Q64246672-D145F356-4933-460D-9611-B2E8E5DD1FDCQ64983362-A1D1DEB8-CF51-4A13-8942-99FB97E5286FQ88597063-DE302EEE-990C-4A97-87F2-DA15E149ADB2Q89490066-F88E8429-121F-4D83-82D5-E09B24F29ABFQ89802826-5976F618-E7CC-4D2E-8BF3-5FD6B2D6009BQ89947688-287D3378-E8BB-48F9-9A03-756AD336DD7CQ89985221-1B04280F-2934-4A59-8BD7-81B26BCF4B31Q90450433-A6020ED9-0C9A-4603-8DA6-EB440227B815Q90732234-985A10D6-23AA-4CF6-80ED-F4E8B8E76B4AQ90821677-4420D0E8-85A4-4A16-923D-952F53CDDDCFQ91198236-2B14BC02-57B6-4561-A661-D7E6C1331B2DQ91210494-852EBC6D-63F4-4DBB-9169-2D395AB60801Q91371142-8C07EF52-2B5A-47E0-A492-7F8B23831B07
P50
description
researcher, ORCID id # 0000-0003-2948-6211
@en
wetenschapper
@nl
name
Michael C Jewett
@ast
Michael C Jewett
@en
Michael C Jewett
@es
Michael C Jewett
@nl
type
label
Michael C Jewett
@ast
Michael C Jewett
@en
Michael C Jewett
@es
Michael C Jewett
@nl
prefLabel
Michael C Jewett
@ast
Michael C Jewett
@en
Michael C Jewett
@es
Michael C Jewett
@nl
P108
P106
P31
P496
0000-0003-2948-6211