A genome-guided approach to the study of novel secondary metabolites in quarry-derived actinomycetes
The recent revival of microbial natural product discovery is motivated by the discovery of cryptic biosynthetic gene clusters (BGCs) with developments in genome sequencing technology. A genome-guided approach was employed in this study to discover natural products produced by the actinomycetes strai...
Saved in:
Main Author: | |
---|---|
Other Authors: | |
Format: | Thesis-Master by Research |
Language: | English |
Published: |
Nanyang Technological University
2019
|
Subjects: | |
Online Access: | https://hdl.handle.net/10356/136568 |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Institution: | Nanyang Technological University |
Language: | English |
id |
sg-ntu-dr.10356-136568 |
---|---|
record_format |
dspace |
spelling |
sg-ntu-dr.10356-1365682023-02-28T18:37:07Z A genome-guided approach to the study of novel secondary metabolites in quarry-derived actinomycetes Tan, Daryn Fu Ern Liang Zhao-Xun School of Biological Sciences ZXLiang@ntu.edu.sg Science::Biological sciences::Biochemistry The recent revival of microbial natural product discovery is motivated by the discovery of cryptic biosynthetic gene clusters (BGCs) with developments in genome sequencing technology. A genome-guided approach was employed in this study to discover natural products produced by the actinomycetes strain Streptomyces sp. P46 isolated from the Pulau Ubin Quarry. Genome sequencing and mining have revealed at least 33 BGCs, of which 18 were considered to be cryptic. Two methods were concurrently used to activate these cryptic BGCs – altering the fermentation media conditions (i.e., one strain many compounds or OSMAC approach) and overexpressing local regulator genes. A novel compound (named as Tasikamide A) with anticancer activity was isolated and its chemical structure was determined. Tasikamide A is putatively produced by BGC 20, a non-ribosomal peptide synthetase (NRPS)-polyketide synthase (PKS) hybrid cluster. Apart from Tasikamide A, several other potentially novel compounds have also been detected through the OSMAC approach and are in the process of being isolated and characterised. In addition to the OSMAC approach, a genetic method was employed to target novel NRPS-PKS hybrid clusters BGCs 12, 14 and 28 to discover novel natural products. An overexpression plasmid was successfully used to express locally activating regulators to generate two overexpression mutant strains (P46 C12-ACT and P46 C28-ACT). The two mutant strains were sub-cultured in several culture media and the organic extract of the culture broth and biomass were subjected to metabolite profiling. Two compounds (a and b) were consistently produced by P46 C28-ACT and were identified to be of interest due to their unique retention time and UV-Vis spectra. While compound a is likely to be furaquinocin A, a known compound, the identity of compound b remains to be established. Unexpectedly, several compounds produced by the wild type P46 strain were not produced by P46 C12- ACT, suggesting that the overexpressed regulator could have been a repressor. Overall, my studies demonstrated that P46 is a biosynthetically talented Streptomyces strain in producing novel natural products and set the stage for the activation of cryptic BGCs using the genetic tools validated in this study. Master of Science 2019-12-30T08:41:20Z 2019-12-30T08:41:20Z 2019 Thesis-Master by Research Tan, D. F. E. (2019). A genome-guided approach to the study of novel secondary metabolites in quarry-derived actinomycetes. Master's thesis, Nanyang Technological University, Singapore. https://hdl.handle.net/10356/136568 10.32657/10356/136568 en This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License (CC BY-NC 4.0). application/pdf Nanyang Technological University |
institution |
Nanyang Technological University |
building |
NTU Library |
continent |
Asia |
country |
Singapore Singapore |
content_provider |
NTU Library |
collection |
DR-NTU |
language |
English |
topic |
Science::Biological sciences::Biochemistry |
spellingShingle |
Science::Biological sciences::Biochemistry Tan, Daryn Fu Ern A genome-guided approach to the study of novel secondary metabolites in quarry-derived actinomycetes |
description |
The recent revival of microbial natural product discovery is motivated by the discovery of cryptic biosynthetic gene clusters (BGCs) with developments in genome sequencing technology. A genome-guided approach was employed in this study to discover natural products produced by the actinomycetes strain Streptomyces sp. P46 isolated from the Pulau Ubin Quarry. Genome sequencing and mining have revealed at least 33 BGCs, of which 18 were considered to be cryptic. Two methods were concurrently used to activate these cryptic BGCs – altering the fermentation media conditions (i.e., one strain many compounds or OSMAC approach) and overexpressing local regulator genes. A novel compound (named as Tasikamide A) with anticancer activity was isolated and its chemical structure was determined. Tasikamide A is putatively produced by BGC 20, a non-ribosomal peptide synthetase (NRPS)-polyketide synthase (PKS) hybrid cluster. Apart from Tasikamide A, several other potentially novel compounds have also been detected through the OSMAC approach and are in the process of being isolated and characterised. In addition to the OSMAC approach, a genetic method was employed to target novel NRPS-PKS hybrid clusters BGCs 12, 14 and 28 to discover novel natural products. An overexpression plasmid was successfully used to express locally activating regulators to generate two overexpression mutant strains (P46 C12-ACT and P46 C28-ACT). The two mutant strains were sub-cultured in several culture media and the organic extract of the culture broth and biomass were subjected to metabolite profiling. Two compounds (a and b) were consistently produced by P46 C28-ACT and were identified to be of interest due to their unique retention time and UV-Vis spectra. While compound a is likely to be furaquinocin A, a known compound, the identity of compound b remains to be established. Unexpectedly, several compounds produced by the wild type P46 strain were not produced by P46 C12- ACT, suggesting that the overexpressed regulator could have been a repressor. Overall, my studies demonstrated that P46 is a biosynthetically talented Streptomyces strain in producing novel natural products and set the stage for the activation of cryptic BGCs using the genetic tools validated in this study. |
author2 |
Liang Zhao-Xun |
author_facet |
Liang Zhao-Xun Tan, Daryn Fu Ern |
format |
Thesis-Master by Research |
author |
Tan, Daryn Fu Ern |
author_sort |
Tan, Daryn Fu Ern |
title |
A genome-guided approach to the study of novel secondary metabolites in quarry-derived actinomycetes |
title_short |
A genome-guided approach to the study of novel secondary metabolites in quarry-derived actinomycetes |
title_full |
A genome-guided approach to the study of novel secondary metabolites in quarry-derived actinomycetes |
title_fullStr |
A genome-guided approach to the study of novel secondary metabolites in quarry-derived actinomycetes |
title_full_unstemmed |
A genome-guided approach to the study of novel secondary metabolites in quarry-derived actinomycetes |
title_sort |
genome-guided approach to the study of novel secondary metabolites in quarry-derived actinomycetes |
publisher |
Nanyang Technological University |
publishDate |
2019 |
url |
https://hdl.handle.net/10356/136568 |
_version_ |
1759854614762487808 |