NMR https://www.ice.mpg.de/246763/group-theses
Chemical and Earth Sciences, Jena (2014) MPG.PuRe 2013 Thesis – Diploma Milde, M.
Chemical and Earth Sciences, Jena (2014) MPG.PuRe 2013 Thesis – Diploma Milde, M.
Behmer, Texas A & M University, USA.
M.; Warr, C. G.; Carlson, J. R.
M.; Warr, C. G.; Carlson, J. R.
M.; Warr, C. G.; Carlson, J. R.
M.; Warr, C. G.; Carlson, J. R.
M.; Warr, C. G.; Carlson, J. R.
A catalytically inactive enzyme enables the formation of free indole for plant defense and communication. • Indole biosynthesis occurs via a pseudoenzyme: Although TSB-like is essential for indole formation, it does not have its own enzyme activity, unlike the enzymes TSB and TSA, which are active in the catalysis of indole to tryptophan.
Florean, M., Schultz, H., Grabe, V., Luck, K., Kunert, G., O’Connor, S.
A catalytically inactive enzyme enables the formation of free indole for plant defense and communication. • Indole biosynthesis occurs via a pseudoenzyme: Although TSB-like is essential for indole formation, it does not have its own enzyme activity, unlike the enzymes TSB and TSA, which are active in the catalysis of indole to tryptophan.
Florean, M., Schultz, H., Grabe, V., Luck, K., Kunert, G., O’Connor, S.
The biosynthesis of the great variety of natural plant products has not yet been elucidated for many medically interesting substances. In a new study, an international team of researchers was able to show how ipecacuanha alkaloids, substances used in traditional medicine, are synthesized. They compared two distantly related plant species and were able to show that although both plant species use a comparable chemical approach, the enzymes they need for synthesis differ and a different starting material is used. Further investigations revealed that the biosynthetic pathways of these complex chemical compounds have developed independently in the two species. These results help to enable the synthesis of these and related substances on a larger scale for medical use.
Colinas, M., Morweiser, C., Â Dittberner, O., Chioca, B., Alam, R., Leucke, H., Nakamura