Pictet-Spengler reaction-based biosynthetic machinery in fungi
The Pictet-Spengler (PS) reaction constructs plant alkaloids such as morphine and camptothecin, but it has not yet been noticed in the fungal kingdom. Here, a silent fungal Pictet-Spenglerase (FPS) gene of Chaetomium globosum 1C51 residing in Epinephelus drummondhayi guts is described and ascertaine...
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my.um.eprints.153852015-12-29T01:55:38Z http://eprints.um.edu.my/15385/ Pictet-Spengler reaction-based biosynthetic machinery in fungi Yan, W. Ge, H.M. Wang, G. Jiang, N. Mei, Y.N. Jiang, R. Li, S.J. Chen, C.J. Jiao, R.H. Xu, Q. Ng, Seik Weng Tan, R.X. Q Science (General) The Pictet-Spengler (PS) reaction constructs plant alkaloids such as morphine and camptothecin, but it has not yet been noticed in the fungal kingdom. Here, a silent fungal Pictet-Spenglerase (FPS) gene of Chaetomium globosum 1C51 residing in Epinephelus drummondhayi guts is described and ascertained to be activable by 1-methyl-L-tryptophan (1-MT). The activated FPS expression enables the PS reaction between 1-MT and flavipin (fungal aldehyde) to form ``unnatural'' natural products with unprecedented skeletons, of which chaetoglines B and F are potently antibacterial with the latter inhibiting acetylcholinesterase. A gene-implied enzyme inhibition (GIEI) strategy has been introduced to address the key steps for PS product diversifications. In aggregation, the work designs and validates an innovative approach that can activate the PS reaction-based fungal biosynthetic machinery to produce unpredictable compounds of unusual and novel structure valuable for new biology and biomedicine. National Academy of Sciences 2014 Article PeerReviewed Yan, W. and Ge, H.M. and Wang, G. and Jiang, N. and Mei, Y.N. and Jiang, R. and Li, S.J. and Chen, C.J. and Jiao, R.H. and Xu, Q. and Ng, Seik Weng and Tan, R.X. (2014) Pictet-Spengler reaction-based biosynthetic machinery in fungi. Proceedings of the National Academy of Sciences of the United States of America (PNAS) ISSN 1091-6490, 111 (51). pp. 18138-18143. |
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Q Science (General) Yan, W. Ge, H.M. Wang, G. Jiang, N. Mei, Y.N. Jiang, R. Li, S.J. Chen, C.J. Jiao, R.H. Xu, Q. Ng, Seik Weng Tan, R.X. Pictet-Spengler reaction-based biosynthetic machinery in fungi |
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The Pictet-Spengler (PS) reaction constructs plant alkaloids such as morphine and camptothecin, but it has not yet been noticed in the fungal kingdom. Here, a silent fungal Pictet-Spenglerase (FPS) gene of Chaetomium globosum 1C51 residing in Epinephelus drummondhayi guts is described and ascertained to be activable by 1-methyl-L-tryptophan (1-MT). The activated FPS expression enables the PS reaction between 1-MT and flavipin (fungal aldehyde) to form ``unnatural'' natural products with unprecedented skeletons, of which chaetoglines B and F are potently antibacterial with the latter inhibiting acetylcholinesterase. A gene-implied enzyme inhibition (GIEI) strategy has been introduced to address the key steps for PS product diversifications. In aggregation, the work designs and validates an innovative approach that can activate the PS reaction-based fungal biosynthetic machinery to produce unpredictable compounds of unusual and novel structure valuable for new biology and biomedicine. |
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Yan, W. Ge, H.M. Wang, G. Jiang, N. Mei, Y.N. Jiang, R. Li, S.J. Chen, C.J. Jiao, R.H. Xu, Q. Ng, Seik Weng Tan, R.X. |
author_facet |
Yan, W. Ge, H.M. Wang, G. Jiang, N. Mei, Y.N. Jiang, R. Li, S.J. Chen, C.J. Jiao, R.H. Xu, Q. Ng, Seik Weng Tan, R.X. |
author_sort |
Yan, W. |
title |
Pictet-Spengler reaction-based biosynthetic machinery in fungi |
title_short |
Pictet-Spengler reaction-based biosynthetic machinery in fungi |
title_full |
Pictet-Spengler reaction-based biosynthetic machinery in fungi |
title_fullStr |
Pictet-Spengler reaction-based biosynthetic machinery in fungi |
title_full_unstemmed |
Pictet-Spengler reaction-based biosynthetic machinery in fungi |
title_sort |
pictet-spengler reaction-based biosynthetic machinery in fungi |
publisher |
National Academy of Sciences |
publishDate |
2014 |
url |
http://eprints.um.edu.my/15385/ |
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1643690042836647936 |
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13.160551 |