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Novel recombinant aminoacylase from Paraburkholderia monticola capable of N-acyl-amino acid synthesis.
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- Applied Microbiology & Biotechnology, 2024, v. 108, n. 1, p. 1, doi. 10.1007/s00253-023-12868-8
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Novel recombinant aminoacylase from Paraburkholderia monticola capable of N-acyl-amino acid synthesis.
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- Applied Microbiology & Biotechnology, 2024, v. 108, n. 1, p. 1, doi. 10.1007/s00253-023-12868-8
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- Article
Novel aminoacylases from Streptomyces griseus DSM 40236 and their recombinant production in Streptomyces lividans.
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- FEBS Open Bio, 2023, v. 13, n. 12, p. 2224, doi. 10.1002/2211-5463.13723
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Biochemical characterisation of a novel broad pH spectrum subtilisin from Fictibacillus arsenicusDSM 15822<sup>T</sup>.
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- FEBS Open Bio, 2023, v. 13, n. 11, p. 2035, doi. 10.1002/2211-5463.13701
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New robust subtilisins from halotolerant and halophilic Bacillaceae.
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- Applied Microbiology & Biotechnology, 2023, v. 107, n. 12, p. 3939, doi. 10.1007/s00253-023-12553-w
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- Article
Chaperone assisted recombinant expression of a mycobacterial aminoacylase in Vibrio natriegens and Escherichia coli capable of N-lauroyl-L-amino acid synthesis.
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- Microbial Cell Factories, 2023, v. 22, n. 1, p. 1, doi. 10.1186/s12934-023-02079-1
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- Article
Biochemical characterization of a novel oxidatively stable, halotolerant, and high‐alkaline subtilisin from Alkalihalobacillus okhensisKh10‐101<sup>T</sup>.
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- FEBS Open Bio, 2022, v. 12, n. 10, p. 1729, doi. 10.1002/2211-5463.13457
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- Article
Phylogenetic survey of the subtilase family and a data-mining-based search for new subtilisins from Bacillaceae.
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- Frontiers in Microbiology, 2022, v. 13, p. 1, doi. 10.3389/fmicb.2022.1017978
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Detection of Acetoin and Diacetyl by a Tobacco Mosaic Virus -Assisted Field-Effect Biosensor.
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- Chemosensors, 2022, v. 10, n. 6, p. 218, doi. 10.3390/chemosensors10060218
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Capacitive Field‐Effect Biosensor Applied for the Detection of Acetoin in Alcoholic Beverages and Fermentation Broths.
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- Physica Status Solidi. A: Applications & Materials Science, 2021, v. 218, n. 13, p. 1, doi. 10.1002/pssa.202000765
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- Article
Elucidation of auxotrophic deficiencies of <italic>Bacillus pumilus</italic> DSM 18097 to develop a defined minimal medium.
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- Microbial Cell Factories, 2018, v. 17, n. 1, p. N.PAG, doi. 10.1186/s12934-018-0956-1
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- Article
High-resolution proteome maps of Bacillus licheniformis cells growing in minimal medium.
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- Proteomics, 2015, v. 15, n. 15, p. 2629, doi. 10.1002/pmic.201400504
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- Article
<i>Bacillus pumilus</i> Reveals a Remarkably High Resistance to Hydrogen Peroxide Provoked Oxidative Stress.
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- PLoS ONE, 2014, v. 9, n. 1, p. 1, doi. 10.1371/journal.pone.0085625
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Stress Responses of the Industrial Workhorse <i>Bacillus licheniformis</i> to Osmotic Challenges.
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- PLoS ONE, 2013, v. 8, n. 11, p. 1, doi. 10.1371/journal.pone.0080956
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The response of Bacillus licheniformis to heat and ethanol stress and the role of the Sig B regulon.
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- Proteomics, 2013, v. 13, n. 14, p. 2140, doi. 10.1002/pmic.201200297
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- Article
RNA-Seq of Bacillus licheniformis: active regulatory RNA features expressed within a productive fermentation.
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- BMC Genomics, 2013, v. 14, n. 1, p. 1, doi. 10.1186/1471-2164-14-667
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- Article
Secretory production of an FAD cofactor-containing cytosolic enzyme (sorbitol-xylitol oxidase from Streptomyces coelicolor) using the twin-arginine translocation ( Tat) pathway of Corynebacterium glutamicum.
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- Microbial Biotechnology, 2013, v. 6, n. 2, p. 202, doi. 10.1111/1751-7915.12005
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Fermentation stage-dependent adaptations of Bacillus licheniformis during enzyme production.
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- Microbial Cell Factories, 2013, v. 12, n. 1, p. 2, doi. 10.1186/1475-2859-12-120
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- Article
Diversity-Oriented Production of Metabolites Derived from Chorismate and Their Use in Organic Synthesis.
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- Angewandte Chemie, 2011, v. 123, n. 34, p. 7927, doi. 10.1002/ange.201103261
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Diversity-Oriented Production of Metabolites Derived from Chorismate and Their Use in Organic Synthesis.
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- Angewandte Chemie International Edition, 2011, v. 50, n. 34, p. 7781, doi. 10.1002/anie.201103261
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Enzymatic deglycation of Amadori products in bacteria: mechanisms, occurrence and physiological functions.
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- Applied Microbiology & Biotechnology, 2011, v. 90, n. 2, p. 399, doi. 10.1007/s00253-010-3083-4
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Transcriptional regulation of the proton translocating NADH dehydrogenase genes (nuoA--N) of Escherichia coli by electron acceptors, electron donors and gene regulators.
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- Molecular Microbiology, 1995, v. 16, n. 3, p. 521, doi. 10.1111/j.1365-2958.1995.tb02416.x
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