Fig. 7. The RMSD profiles of the region with high (RMSD H) and low (RMSD L) mobility from the simulation of WT (a), S491A (b) and F482/S491A (c) in complex with the pinyl cation.Published as part of Xu, Jingwei, Peng, Guanzu, Xu, Jinkun, Li, Yi, Tong, Li & Yang, Dong, 2021, Probing of the plasticity of the active site in pinene synthase elucidates its potential evolutionary mechanism, pp. 1-10 in Phytochemistry (112573) 181 on page 8, DOI: 10.1016/j.phytochem.2020.112573, http://zenodo.org/record/829106
<p>α-Pinene is a natural and active monoterpene, which is widely used as a flavoring agent and in fr...
<p>α-Pinene is a natural and active monoterpene, which is widely used as a flavoring agent and in fr...
Fig. 8. Molecular models of Camptotheca CYP72A564, CYP72A565 and CYP72A730. (A) Backbone overlays of...
Fig. 6. S491A mutation increases the rigidity of the active pocket when it binds the pinyl cation. R...
Fig. 4. Conformational differences in the pinyl cation in WT and F482Y as demonstrated by molecular ...
Xu, Jingwei, Peng, Guanzu, Xu, Jinkun, Li, Yi, Tong, Li, Yang, Dong (2021): Probing of the plasticit...
Fig. 1. a, The proposed reaction mechanism for the synthesis of limonene, pinene and sabinene. b, Th...
Fig. 2. Converting pinene synthase to sabinene synthase by mutations on 482 position. Chromatograms ...
Fig. 5. The effect of the S491A mutation. Chromatograms in a, b and c show the GC-MS analysis of ter...
Fig. 3. Hybrid quadrupole-orbitrap GC-MS/MS. a shows the chromatogram of terpene products of F482L. ...
2.1. Homology modeling of P. lactiflora pinene synthase The crystal structures of pinene synthase...
Fig. 1. Chemical structures of the pinenes with their two enantiomers: (+)-α-pinene (1), ()-α-pinene...
Pinene, a natural active monoterpene, is widely used as a flavoring agent, perfume, medicine, and bi...
<p>α-Pinene is a natural and active monoterpene, which is widely used as a flavoring agent and in fr...
<p>α-Pinene is a natural and active monoterpene, which is widely used as a flavoring agent and in fr...
<p>α-Pinene is a natural and active monoterpene, which is widely used as a flavoring agent and in fr...
<p>α-Pinene is a natural and active monoterpene, which is widely used as a flavoring agent and in fr...
Fig. 8. Molecular models of Camptotheca CYP72A564, CYP72A565 and CYP72A730. (A) Backbone overlays of...
Fig. 6. S491A mutation increases the rigidity of the active pocket when it binds the pinyl cation. R...
Fig. 4. Conformational differences in the pinyl cation in WT and F482Y as demonstrated by molecular ...
Xu, Jingwei, Peng, Guanzu, Xu, Jinkun, Li, Yi, Tong, Li, Yang, Dong (2021): Probing of the plasticit...
Fig. 1. a, The proposed reaction mechanism for the synthesis of limonene, pinene and sabinene. b, Th...
Fig. 2. Converting pinene synthase to sabinene synthase by mutations on 482 position. Chromatograms ...
Fig. 5. The effect of the S491A mutation. Chromatograms in a, b and c show the GC-MS analysis of ter...
Fig. 3. Hybrid quadrupole-orbitrap GC-MS/MS. a shows the chromatogram of terpene products of F482L. ...
2.1. Homology modeling of P. lactiflora pinene synthase The crystal structures of pinene synthase...
Fig. 1. Chemical structures of the pinenes with their two enantiomers: (+)-α-pinene (1), ()-α-pinene...
Pinene, a natural active monoterpene, is widely used as a flavoring agent, perfume, medicine, and bi...
<p>α-Pinene is a natural and active monoterpene, which is widely used as a flavoring agent and in fr...
<p>α-Pinene is a natural and active monoterpene, which is widely used as a flavoring agent and in fr...
<p>α-Pinene is a natural and active monoterpene, which is widely used as a flavoring agent and in fr...
<p>α-Pinene is a natural and active monoterpene, which is widely used as a flavoring agent and in fr...
Fig. 8. Molecular models of Camptotheca CYP72A564, CYP72A565 and CYP72A730. (A) Backbone overlays of...