Download presentation
Presentation is loading. Please wait.
Published byRiley Bookbinder Modified over 9 years ago
1
Rapid, Small-scale Dereplication of Bioactive Extracts John Blunt University of Canterbury New Zealand 1
2
~ 145,000 known natural products Probability for rediscovery very high Efficient dereplication processes required is differentiating extracts that contain novel metabolites from those with known natural products Dereplication Bioactive Discovery 2abc
3
Scale of Dereplication Exercise 0.5 – 2 mg extract 4 mL agar slope Petri dish Bioassay and HPLC/UV/MS/NMR evaluation 100 mg sponge 3a
4
~0.6 mg crude extract separated on analytical C18 column DAD & ELSD detection Eluant collected in microtitre plate 1 mL/min, 250 L/well Daughter plate submitted to bioassay to locate bioactive components (Master plate submitted for automated ES-MS analysis of each well) 4
5
Separation of 600 g fungal extract (F8095) using acetonitrile/methanol gradient Jackson Lin Sun 5
6
6
7
7
8
M+Na HPLC peak F8095-1 8
9
Search against ~44,000 unique compounds in AntiMarin for those with M+Na = 407 AntiMarin – combination of compound data from MarinLit (~20,000 marine natural products) and AntiBase (~33,000 microbial natural products) All compounds coded for 1 H NMR-recognisable features 9 ab
10
10
11
solvent 3 x doublet methyls 1 H CapNMR spectrum of 15 g of F8095-1 CD 3 OD, 2 min, presat 11a
12
12
13
Only 1 compound found - details match with F8095-1 13a
14
Now examine contents of microtitre plate well containing F8095-2 14
15
M-H - +ve ion MS of F8095-2 not useful, but –ve ion MS suggests M-H = 193 15
16
1 H CapNMR spectrum of 6 g of F8095-2 CD 3 OD, 2 min, presat Recognise 1 doublet methyl signal, and 2 aromatic singlets probably indicating 1,2,3,5-tetrasubstitution pattern solvent 1 x doublet methyl 2 x aromatic singlet H 16
17
Search in AntiMarin for 1 doublet CH 3, 1,2,3,5-substituted benzene, and Mr = 194 One hit only – data matches that for F8095-2 17
18
Now examine contents of microtitre plate well containing F8095-7 18
19
+ve ion MS of F8095-7 shows M+Na = 669 Search in AntiMarin gives 19 hits 19a
20
1 H CapNMR spectrum of 13 g of F8095-7 CD 3 OD, 2 min, presat Recognise 5 doublet methyl signals solvent 5 x doublet methyls 20
21
Search in AntiMarin for 5 doublet CH 3 s, and M+Na = 669 One hit only – data matches that for F8095-7 21
22
7 compounds from F8095 identified by HPLC-microtitre-MS-NMR/database method 15 g 6 g 16 g 8 g 12 g 22
23
time costcost The pathway to bioactive compound identification complete structure/dereplication sample extract bioassay scale-up & extraction bioassay-guided fractionation pure compound ~1 mg spectroscopic analysis HPLC-Bioassay-UV-MS ~5-50 g HPLC-bioassay-(UV)-(MS)-NMR ~500 g crude extract database searching dereplication spectroscopic analysis 2-50 g complete structure J. Nat. Prod., 2008, 71, 1595-99. 23abcdef
24
Acknowledgements Development of the concept and techniques for the use of HPLC-microtitre plate-capillary NMR: John Blunt & Murray Munro (UC) Kirk Gustafson (MTDP, NCI, Frederick MD) Development of the concept of and construction of databases for use in dereplication: John Blunt & Murray Munro (UC) Hartmut Laatsch (University of Göttingen) Preparation of samples for demonstration of techniques: Gill Ellis, Sultan Sadia, Jackson Lin Sun 24
Similar presentations
© 2025 SlidePlayer.com. Inc.
All rights reserved.