Mai-Truc Pham
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Previous Organizations / Institutes
The organizations / institutes from the scholar's other articles in the past ten years
Mai-Truc Pham has a total of 9 co-authors. Here are the top co-authors by number of shared publications:
Adnane Aouidate
John Innes Centre, Norwich Research Park, Norwich, UK
1 shared publicationAlan Houghton
John Innes Centre, Norwich Research Park, Norwich, UK
1 shared publication- Anne Osbourn
Department of Biochemistry and Metabolism, John Innes Centre, Norwich Research Park, Norwich NR4 7UH, UK
1 shared publication - Hsiao-Ching Lin
Institute of Biological Chemistry, Academia Sinica
1 shared publication Rebecca Casson
John Innes Centre, Norwich Research Park, Norwich, UK
1 shared publication- Rocky D. Payet
School of Biological Sciences, University of East Anglia, Norwich Research Park, Norwich, U.K.
1 shared publication
Latest Publications
- Open Access
- 3 July 2025
- Published by Springer Nature in The EMBO Journal
- Vol. 44 (16) , 4409-4418
A million shades of green: understanding and harnessing plant metabolic diversity
Recent developments in single-cell -omic and metabolite imaging technologies and the increasing availability of high-quality genome assemblies are having a transformative impact on the way research is carried out into plant specialised metabolism. Integrating these technologies into pathway discovery projects is therefore highly advantageous. Here, we present a general introduction into methods and workflows in specialised metabolism research. We review a range of recent methodologies, highlighting what they might be used for and common pitfalls which may be encountered. Finally, we provide a practical guide on how these technologies may be incorporated into a specialised metabolic pathway discovery pipeline for researchers who are new to the field.
- 3 July 2025
- Published by Springer Nature in The EMBO Journal
- Vol. 44 (16) , 4409-4418
Open AccessA million shades of green: understanding and harnessing plant metabolic diversity
Recent developments in single-cell -omic and metabolite imaging technologies and the increasing availability of high-quality genome assemblies are having a transformative impact on the way research is carried out into plant specialised metabolism. Integrating these technologies into pathway discovery projects is therefore highly advantageous. Here, we present a general introduction into methods and workflows in specialised metabolism research. We review a range of recent methodologies, highlighting what they might be used for and common pitfalls which may be encountered. Finally, we provide a practical guide on how these technologies may be incorporated into a specialised metabolic pathway discovery pipeline for researchers who are new to the field.
- 26 May 2022
- Published by American Chemical Society (ACS) in Organic Letters
- Vol. 24 (22) , 4064-4069
Biosynthesis of Piperazine-Derived Diazabicyclic Alkaloids Involves a Nonribosomal Peptide Synthetase and Subsequent Tailoring by a Multifunctional Cytochrome P450 Enzyme
Piperazine-derived diazabicycles are privileged structures found in natural products and synthetic chemical entities, including therapeutic agents. Herein, we deciphered the biosynthesis of two unique classes of diazabicyclic alkaloids, fischerazines A-C. Notably, we characterized a multifunctional P450 monooxygenase NfiC that installs ortho-dihydroxyl groups on the dibenzyl-piperazines, in turn triggering a range of NfiC-catalyzed and spontaneous cyclization events.
- 26 May 2022
- Published by American Chemical Society (ACS) in Organic Letters
- Vol. 24 (22) , 4064-4069
Biosynthesis of Piperazine-Derived Diazabicyclic Alkaloids Involves a Nonribosomal Peptide Synthetase and Subsequent Tailoring by a Multifunctional Cytochrome P450 Enzyme
Piperazine-derived diazabicycles are privileged structures found in natural products and synthetic chemical entities, including therapeutic agents. Herein, we deciphered the biosynthesis of two unique classes of diazabicyclic alkaloids, fischerazines A-C. Notably, we characterized a multifunctional P450 monooxygenase NfiC that installs ortho-dihydroxyl groups on the dibenzyl-piperazines, in turn triggering a range of NfiC-catalyzed and spontaneous cyclization events.