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Applied Microbiology and Biotechnology, ISSN 0175-7598, 9/2014, Volume 98, Issue 17, pp. 7399 - 7408
Journal Article
Journal Article
Chemical Physics Letters, ISSN 0009-2614, 02/2019, Volume 716, pp. 247 - 251
[Display omitted] •The biosynthesis of R-PAC by AHAS is addressed by MD dynamics.•The N1′ atom of HEThDP should be protonated and the N4′ atom as... 
YEAST | L-PHENYLACETYLCARBINOL | ACETOHYDROXYACID SYNTHASE | PATHWAY | PHYSICS, ATOMIC, MOLECULAR & CHEMICAL | CHEMISTRY, PHYSICAL | CHIRAL SYNTHESIS | AUTOMATION | GENERAL FORCE-FIELD | CHARMM | SIMULATION
Journal Article
Journal of Biotechnology, ISSN 0168-1656, 01/2020, Volume 308, pp. 27 - 34
•Effect of gene deletions on l-PAC formation in S. cerevisiae was assessed•Six mutants, namely Δrpe1, Δpda1, Δadh3, Δadh1, Δzwf1 and Δpdc1, were predicted... 
Metabolic engineering | Flux balance analysis | l-phenylacetylcarbinol | Saccharomyces cerevisiae | OptGene | (R)-PHENYLACETYLCARBINOL PRODUCTION | CARBINOL | RECONSTRUCTION | PREDICTION | YEAST | L-phenylacetylcarbinol | BIOTRANSFORMATION | BENZALDEHYDE | BIOTECHNOLOGY & APPLIED MICROBIOLOGY | ENZYMES | BIOSYNTHESIS | PYRUVATE DECARBOXYLASE
Journal Article
Journal Article
Process Biochemistry, ISSN 1359-5113, 10/2018, Volume 73, pp. 74 - 81
[Display omitted] •Whole-cell biocatalysts were constructed for (1R, 2S)-norephedrine (NE) production.•The conversion yield of L-phenylacetylcarbinol was... 
l-phenylacetylcarbinol | (1R, 2S)-norephedrine | Biotransformation | ω-transaminase | Conversion yield | Acetohydroxyacid synthase I | L-phenylacetylcarbinol
Journal Article
Process Biochemistry, ISSN 1359-5113, 10/2018, Volume 73, p. 74
In this study, a combined whole-cell biotransformation process was used for efficient synthesis of optically pure (1R, 2S)-norephedrine [(1R, 2S)-NE]. The... 
Adenosine | Temperature | Alanine | Phenylacetylcarbinol | Purification | Transaminase | Benzaldehyde | Adenosine diphosphate | Pyruvic acid | L-Phenylacetylcarbinol | Biochemistry | Entropy | Biocatalysts | Conversion | Stereoselectivity | Acetohydroxyacid synthase | Synthesis | E coli | Biotransformation | L-Alanine | Yield | Recombinant
Journal Article
by Wu, XR and Fei, MD and Chen, Y and Wang, ZQ and Chen, YJ
APPLIED MICROBIOLOGY AND BIOTECHNOLOGY, ISSN 0175-7598, 09/2014, Volume 98, Issue 17, pp. 7399 - 7408
l-Norephedrine, a natural plant alkaloid, possesses similar activity as ephedrine and can be used as a vicinal amino alcohol for the asymmetric synthesis of a... 
L-Norephedrine | ASYMMETRIC-SYNTHESIS | (R)-PHENYLACETYLCARBINOL PRODUCTION | CANDIDA-UTILIS | ENANTIOMERS | L-HOMOPHENYLALANINE | L-Phenylacetylcarbinol | Biosynthesis | CHIRAL AMINES | BIOCATALYSIS | omega-Transaminase | BIOTECHNOLOGY & APPLIED MICROBIOLOGY | VIBRIO-FLUVIALIS JS17 | KINETIC RESOLUTION | SUBSTRATE | Pyruvate decarboxylase
Journal Article
Guocheng Gongcheng Xuebao/The Chinese Journal of Process Engineering, ISSN 1009-606X, 02/2009, Volume 9, Issue 1, pp. 190 - 199
Journal Article
Journal Article
Biotechnology and Bioengineering, ISSN 0006-3592, 01/1996, Volume 49, Issue 1, pp. 52 - 62
Biotransformation of benzaldehyde to L‐phenylacetylcarbinol (L‐PAC) as a key intermediate for L‐ephedrine synthesis has been evaluated using pyruvate... 
Candida utilis | biotransformation | benzaldehyde | L‐phenylacetylcarbinol | pyruvate decarboxylase | L-phenylacetylcarbinol
Journal Article