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. 2016 Jul 14;11(7):e0159348. doi: 10.1371/journal.pone.0159348

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© 2016 Jain et al

This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

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Fig 2 — (A) Histogram depicting activity of purified AtGLYI2 protein in presence of various metal ions. AtGLYI2 was demetalled using EDTA and then, reconstituted with different metal ions. The activity was checked after 2 h and 4 h of reconstitution. AtGLYI2 showed maximal activity with MnCl₂ followed by CoCl₂, NiCl₂ and CdCl₂. This behavior is characteristic of Zn²⁺ dependent GLYI enzymes. (B) Histogram depicting activity of purified AtGLYI3 and AtGLYI6 in presence and absence of Ni²⁺. (C) Histogram depicting activity of thrombin cleaved and purified AtGLYI3 and AtGLYI6 (to remove His tag) in presence and absence of Ni²⁺.