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. 2015 Apr 24;8(4):665–672. doi: 10.1111/1751-7915.12278

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© 2015 The Authors. Microbial Biotechnology published by John Wiley & Sons Ltd and Society for Applied Microbiology.

This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.

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Fig 3 — Transaminase-catalyzed transformation of 12-aminododecanoic acid.A. LC-MS trace showing complete conversion of 12-aminododecanoic acid material into dodecanoic acid-12-semialdehyde by KES24511, KES23458 and KES23360. A negative control (no transaminase enzyme) is also shown. The inset magnifies the 12-aminododecanoic acid, which is far less UV-absorbant than dodecanoic acid-12-semialdehyde.B. LC-MS trace showing alanine (co-product) formation via 12-aminododecanoic acid-dependent amination of pyruvate by KES24511, KES23458 and KES23360. Peaks corresponding to pyruvate and l-alanine were verified against pure standards.