Design and Optimization of Short DNA Sequences That Can Be Used as 5′ Fusion Partners for High-Level Expression of Heterologous Genes in Escherichia coli

Non-Invasive Analysis of Recombinant mRNA Stability in Escherichia coli by a Combination of Transcriptional Inducer Wash-Out and qRT-PCR

(2013) Veronika Kucharova et al.   PLoS One

Combinatorial Mutagenesis and Selection of Improved Signal Sequences and Their Application for High-Level Production of Translocated Heterologous Proteins in Escherichia coli

(2012) Tonje Marita Bjerkan Heggeset et al.   APPLIED AND ENVIRONMENTAL MICROBIOLOGY

Industrial production of recombinant therapeutics in Escherichia coli and its recent advancements

(2012) Chung-Jr Huang et al.   JOURNAL OF INDUSTRIAL MICROBIOLOGY & BIOTECHNOLOGY

Exploring the 5′-UTR DNA region as a target for optimizing recombinant gene expression from the strong and inducible Pm promoter in Escherichia coli

(2011) Laila Berg et al.   JOURNAL OF BIOTECHNOLOGY

SignalP 4.0: discriminating signal peptides from transmembrane regions

(2011) Thomas Nordahl Petersen et al.   NATURE METHODS

S1 ribosomal protein and the interplay between translation and mRNA decay

(2011) Francesco Delvillani et al.   NUCLEIC ACIDS RESEARCH

An Evolutionarily Conserved Mechanism for Controlling the Efficiency of Protein Translation

(2010) Tamir Tuller et al.   CELL

Random Mutagenesis of the Pm Promoter as a Powerful Strategy for Improvement of Recombinant-Gene Expression

(2009) I. Bakke et al.   APPLIED AND ENVIRONMENTAL MICROBIOLOGY

Quantitative correlation between mRNA secondary structure around the region downstream of the initiation codon and translational efficiency inEscherichia coli

(2009) Sang Woo Seo et al.   BIOTECHNOLOGY AND BIOENGINEERING

Automated design of synthetic ribosome binding sites to control protein expression

(2009) Howard M Salis et al.   NATURE BIOTECHNOLOGY

Coding-Sequence Determinants of Gene Expression in Escherichia coli

(2009) G. Kudla et al.   SCIENCE

The expression of recombinant genes inEscherichia colican be strongly stimulated at the transcript production level by mutating the DNA-region corresponding to the 5′-untranslated part of mRNA

(2009) Laila Berg et al.   Microbial Biotechnology

A structural view of translation initiation in bacteria

(2008) A. Simonetti et al.   CELLULAR AND MOLECULAR LIFE SCIENCES

The bacterial enzyme RppH triggers messenger RNA degradation by 5′ pyrophosphate removal

(2008) Atilio Deana et al.   NATURE

Secretory signal sequence non-optimal codons are required for expression and export of β-lactamase

(2007) Yaramah M. Zalucki et al.   BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS