ArticleBioresources and bioprocessing2017
A food-grade expression system for d-psicose 3-epimerase production in
Article in Bioresources and bioprocessing, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.
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Who cites it
6 citing papers in PubMed, 21 citations in OpenAlex.
- Development of a lactose-complemented antibiotic-free host-vector platform for stable enzyme expression in Limosilactobacillus fermentum 217 - 82.World journal of microbiology & biotechnology · 2026Article
- Antibiotic-Free Expression of γ-Glutamyl Transpeptidase inMolecules (Basel, Switzerland) · 2026Article
- Produce D-allulose from non-food biomass by integrating corn stalk hydrolysis with whole-cell catalysis.Frontiers in bioengineering and biotechnology · 2023Article
- A 4-α-Glucanotransferase from Thermus thermophilus HB8: Secretory Expression and Characterization.Current microbiology · 2022Article
- Overexpression ofFrontiers in microbiology · 2022Article
- Developing rapid growingMetabolic engineering communications · 2020Article
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Authors and funding
5 authors at 2 institutions in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
backgroundFood-grade expression systems require that the resultant strains should only contain materials from food-safe microorganisms, and no antibiotic resistance marker can be utilized. To develop a food-grade expression system for d-psicose 3-epimerase production, we use an alanine racemase-encoding gene as selection marker in
resultsIn this study, the d-alanine racemase-encoding gene
conclusionThe alanine racemase-encoding gene can be used as a selection marker, and the food-grade expression system was suitable for heterologous proteins production in
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