Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Identification of the translational start site of codon-optimized mCherry in Mycobacterium tuberculosis.

BMC research notes - 17 Jun 2014

Carroll Paul, Muwanguzi-Karugaba Julian, Melief Eduard, Files Megan, Parish Tanya

Abstract excerpt

BACKGROUND: Fluorescent proteins are used widely as reporter genes in many organisms. We previously codon-optimized mCherry for Mycobacterium tuberculosis and generated expression constructs with high level expression in mycobacteria with multiple uses in vitro and in vivo. However, little is kno...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Codon, Initiator
Share to Codon, Terminator
Share to Genes, Reporter

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Luminescent Proteins

Share to Mycobacterium tuberculosis

Share to Open Reading Frames

Share to Peptide Chain Initiation, Translational

Share to Red Fluorescent Protein

Source

Open in PubMed Open full text

Identifiers

PMID: 24934902
DOI: 10.1186/1756-0500-7-366
PMCID: PMC4091752

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-24934902-2026-09-04.2. Manifest publication-graph-cohort-2026-09-04.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 4 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Identification of the translational start site of codon-optimized mCherry in Mycobacterium tuberculosis.PMID 24934902Read ↗

Production of recombinant proteins in Mycobacterium smegmatis for structural and functional studiesSemantic proximity Read ↗

Genetic incorporation of unnatural amino acids into proteins in Mycobacterium tuberculosis.Semantic proximity Read ↗

Translational regulation in mycobacteria and its implications for pathogenicitySemantic proximity Read ↗

Efficient construction of unmarked recombinant mycobacteria using an improved system.Semantic proximity Read ↗

Optimization of Codon Usage Enhances the Immunogenicity of a DNA Vaccine Encoding Mycobacterial Antigen Ag85BSemantic proximity Read ↗

The pMy vector series: A versatile cloning platform for the recombinant production of mycobacterial proteins in Mycobacterium smegmatisSemantic proximity Read ↗

Clickable methionine as a universal probe for labelling intracellular bacteriaSemantic proximity Read ↗

Translational misreading in Mycobacterium smegmatis increases in stationary phase.Semantic proximity Read ↗

Construction and application of mycobacterial reporter transposons.Semantic proximity Read ↗

Codon-optimized fluorescent mTFP and mCherry for microscopic visualization and genetic counterselection of streptococci and enterococci.Semantic proximity Read ↗

Development of Assay Systems for Amber Codon Decoding at the Steps of Initiation and Elongation in Mycobacteria.Semantic proximity Read ↗

The impact of leadered and leaderless gene structures on translation efficiency, transcript stability, and predicted transcription rates in <i>Mycobacterium smegmatis</i>Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.