Secondary metabolite discovery

Authors: orcid logoPaul Zierep avatar Paul Zierep
Overview
Creative Commons License: CC-BY Questions:

  • How to discover secondary metabolites produced by microorganisms ?

  • How to identify the discovered secondary metabolites in compound libraries ?

  • How to bridge workflow steps using custom scripts ?

Objectives:

  • Gene cluster prediction using antiSMAHS.

  • Extraction of gene cluster products using a custom script.

  • Query of the products in compound libraries using cheminformatic tools.

Requirements:
Time estimation: 3 hours
Supporting Materials:
Published: Feb 21, 2024
Last modification: Feb 21, 2024
License: Tutorial Content is licensed under Creative Commons Attribution 4.0 International License. The GTN Framework is licensed under MIT
PURL: https://gxy.io/GTN:T00420
Revision: 3

Genome mining is an important source for various bio-active compounds such as antibiotics and fungicides (Adamek et al. 2017). One challenge in secondary metabolite discovery using genome mining requires to annotate biosynthetic gene clusters (BGCs) using dedicated tools such as antiSMASH (Blin et al. 2023) as well as to query the discovered secondary metabolites against compound libraries (Zierep et al. 2020) in order to identify weather they might posses bio-active properties.

In this toturial we will:

  • Annotate biosynthetic gene clusters (BGCs) using antiSMASH.
  • Extract the predicted compounds as SMILES using a custom script.
  • Query the predicted compounds agains the MIBiG (Terlouw et al. 2023) which is a dedicated BGC database.
  • Characterize the predicted compounds using dedicated cheminformatic tools.
Agenda

In this tutorial, we will cover:

  1. Galaxy and data preparation
    1. Get data
  2. Biosynthetic gene clusters (BGCs) detection and compound extraction
    1. Download a bacterial genome with NCBI Accession Download
    2. Detect BGCs and predict NRPS / PKS metabolite structures with Antismash
    3. Collapse single BGC Genbank files into one with Collapse Collection
  3. Use custom scripts in Galaxy to bridge between workflow steps
    1. Integrate a custom script into the workflow using Interactive JupyTool and notebook
  4. Cheminformatics
    1. Convert the table into a two column table
    2. Remove duplicated molecules
    3. Generate fingerprints for the predicted secondary metabolites and the target database with Molecule to fingerprint
    4. Compare prediction with target DB using Similarity Search
    5. Determine the novelty of the compounds using Natural Product likeness calculator
    6. Check Drug-likeness of the predicted compounds
  5. Conclusion

Galaxy and data preparation

Any analysis should get its own Galaxy history. So let’s start by creating a new one and get the data into it.

Get data

Hands-on: History Creation and Data Upload

  1. Create a new history for this tutorial

    Click the icon at the top of the history panel:

    UI for creating new history

  2. Rename the history

    1. Click on (Edit) next to the history name (which by default is “Unnamed history”)
    2. Type the new name
    3. Click on Save

    If you do not have the (Edit) next to the history name:

    1. Click on Unnamed history (or the current name of the history) (Click to rename history) at the top of your history panel
    2. Type the new name
    3. Press Enter

  3. Import the files from Zenodo or from the shared data library (GTN - Material -> genome-annotation -> Secondary metabolite discovery):

    https://zenodo.org/record/10652998/files/MIBiG_compounds_3.0.sdf
https://zenodo.org/record/10652998/files/gbk2features.ipynb

    For this training we need a custom jupyter notebook and a compound library.

    • Copy the link location

    • Click Upload Data at the top of the tool panel

    • Select Paste/Fetch Data

    • Paste the link(s) into the text field

    • Press Start

    • Close the window

  4. Rename the datasets

  5. Check that the datatype is correct

    • Click on the pencil icon for the dataset to edit its attributes
    • In the central panel, click Datatypes tab on the top
    • In the Assign Datatype, select datatypes from “New type” dropdown
      • Tip: you can start typing the datatype into the field to filter the dropdown menu
    • Click the Save button

  6. Add useful tags to your datasets

    1. Click on the dataset to expand it
    2. Click on Add Tags
    3. Add a tag starting with #
      • Tags starting with # will be automatically propagated to the outputs of tools using this dataset.
    4. Press Enter
    5. Check that the tag appears below the dataset name

Biosynthetic gene clusters (BGCs) detection and compound extraction

The general idea of this tutorial is described in the flowchart below. Zierep et. al. previously created a workflow that combines BGC prediction with natural compound screening in their webserver SeMPI 2.0 (Zierep et al. 2020). Here, we want to reproduce the workflow using Galaxy, which allows to adjust the workflow and combine it with other tools and databases. E.g. the workflow could be combined with metagenomic workflows, that allow to screen a vast amount of metagenome assembly genomes (MAGs) for potential novel bioactive compounds.

Overview flowchart. Open image in new tab

Figure 1: Overview flowchart of the workflow.

Download a bacterial genome with NCBI Accession Download

Hands-on: Task description
  1. NCBI Accession Download ( Galaxy version 0.2.8+galaxy0) with the following parameters:
    • “Select source for IDs”: Direct Entry
      • “ID List”: AL645882.2
    • “Molecule Type”: Nucleotide
    Comment: Genome download

    This downloads the Streptomyces coelicolor A3(2) complete genome, which should be a great source for biosynthetic gene clusters (BGCs).

Detect BGCs and predict NRPS / PKS metabolite structures with Antismash

Hands-on: Task description
  1. Antismash ( Galaxy version 6.1.1+galaxy1) with the following parameters:
    • “Sequence file in GenBank,EMBL or FASTA format”: Downloaded Files (output of NCBI Accession Download )
    • “Taxonomic classification of input sequence”: Bacteria
    Comment: BGC detection

    This step uses Antismash for BGC detection. Another tool that could be used is prism. But prism can only be used via a web server and is therefore not integrable into Galaxy workflows.

Question
  1. How many BGCs are detected for the Streptomyces coelicolor A3(2) complete genome ?
  2. How many BGCs are of type NRPS ?
  1. In the HTML report of Antismash you can find 27 BGCs of various types.
  2. Of those 27 BGCs 4 are pure NRPS and one more is classified as NRPS-like.

Collapse single BGC Genbank files into one with Collapse Collection

Hands-on: Task description
  1. Collapse Collection ( Galaxy version 5.1.0) with the following parameters:
    • “Collection of files to collapse into single dataset”: Genbank (output of Antismash )
    • “Prepend File name”: Yes
    Comment: Collapse Genbank files

    Antismash produces one Genbank file for each cluster. Genbank files can contain multiple records. For downstream analysis it is more convenient to combine all clusters into one file.

Use custom scripts in Galaxy to bridge between workflow steps

Integrate a custom script into the workflow using Interactive JupyTool and notebook

For the next steps we need to extract the SMILES representations of the predicted BGC metabolites. And convert it into the .smi format (basically a tabular format that contains names and structures of chemical compounds).

The SMILES representations of the predicted BGC metabolites are stored as features of the clusters in the Genbank files.

     cand_cluster    1..49828
                     /SMILES="NC(CCCN)C(=O)NC(C(O)C)C(=O)NC(CCCN)C(=O)O"
                     /candidate_cluster_number="1"
                     /contig_edge="False"
                     /detection_rules="cds(Condensation and (AMP-binding or
                     A-OX))"
                     /kind="single"
                     /product="NRPS"
                     /protoclusters="1"
                     /tool="antismash"

There are various tools that can convert Genbank files into GFF (like customGbkToGff ( Galaxy version 20.1.0.0) and genbank2gff3 ( Galaxy version 1.1)). From the GFF one could extract the SMILES string via regex. However, unfortunately both tools seem to have difficulty to parse SMILES and introduce artefacts like:

SMILES=CC(%3DO)C(%3DO)O

Therefore we need to quickly prototype our own script, that allows to generate the desired SMILES representations. This is in fact a great chance to demonstrate how the interactive Interactive JupyTool and notebook can be used to connect workflow steps, for which there is no dedicated tool yet available in Galaxy, showing the flexible nature of Galaxy.

Hands-on: Task description
  1. Interactive JupyTool and notebook with the following parameters:
    • “Do you already have a notebook?”: Load a previous notebook
      • “IPython Notebook”: gbk2features.ipynb (from your history)
      • “Execute notebook and return a new one.”: Yes
    • In “User inputs”:
      • “Insert User inputs”
        • “Name for parameter”: dataset (a file called dataset will be created in the notebook in the folder galaxy_inputs)
        • “Choose the input type”: Dataset
          • “Select value”: Collapse Genbank files (output of Collapse Collection )
    Comment: Interactive JupyTool and notebook

    JupyTool notebooks can be executed interactively, which allows to run any code (python / R / bash) dynamically or as a normal tool itself, that executes a provide script and return the output. More information about the JupyTool can be found in the Interactive JupyTool Tutorial.

In this workflow the jupyter notebook is executed and the output collected. If you want to run the notebook interactively. Rerun the tool and set the option “Execute notebook and return a new one.”: No. Now the notebook will start up interactively and you can play around the the python code.

The code we provide for the notebook looks like this:

from Bio import SeqIO
import pandas as pd
import numpy as np

input_path = "galaxy_inputs"

use_qualifiers = ["SMILES"] 

feature_list = []

for folder in os.listdir(input_path):

    folder_path = os.path.join(input_path, folder)

    if os.path.isdir(folder_path):

        for file in os.listdir(folder_path):
            file_path = os.path.join(folder_path, file)
            if '.genbank' in file:
                for record in SeqIO.parse(file_path, "genbank"):
                    #print(record)
                    
                    for feat in record.features:

                        combined_features = {}
                        combined_features['ID'] = record.id
                        combined_features['Name'] = record.name
                        combined_features['Type'] = feat.type
                        combined_features['Start'] = feat.location.start
                        combined_features['End'] = feat.location.end
                        combined_features['Strand'] = feat.location.strand

                        for qualifier in feat.qualifiers.items():
                                combined_features[qualifier[0]] = qualifier[1][0]
                        
                        feature_list.append(combined_features)
                
df = pd.DataFrame(feature_list)

# df trimming is simpler with pandas
df.replace('', np.nan, inplace=True)
df = df.dropna(subset=use_qualifiers)

#remove extra space antiSMASH bug (https://github.com/antismash/antismash/issues/694)
df['SMILES'] = df['SMILES'].str.replace(' ', '')


#only keep what is needed downstream
df = df.loc[:,['ID', 'Name', 'Type', 'Start', 'End', 'Strand', 'SMILES']]

df.to_csv("outputs/collection/feature_table.tsv", sep="\t")
Question
  1. What does the notebook do ?
  1. The notebook creates a table with a row for each SMILES qualifier.

Cheminformatics

Now, that we have predicted the products of the BGCs found in the Streptomyces coelicolor A3(2) complete genome, we can compare the chemical structures of the prediction with natural compound libraries to see if some of the compounds are similar to other compounds with known bio-activte properties. Those compounds should be further investigated. The natural compound library we are using here comprises all the compounds found in the MIBiG (Terlouw et al. 2023).

Convert the table into a two column table

The next two steps convert the generated table into the .smi format. The .smi format is basically a specific table format where the first column is a chemical structure and the second column the ID or name of the compound. The table must not have a header.

Hands-on: Table to smi format conversion
  1. Text reformatting ( Galaxy version 1.1.2) with the following parameters:
    • “File to process”: output_collection (output of Interactive JupyTool and notebook )
    • “AWK Program”: {print $8, $2-$5-$6}
  2. Remove beginning with the following parameters:
    • “from”: outfile (output of Text reformatting )

  3. Now, that the table is indeed the same as the .smi format it can also be converted into .smi.

    • Click on the pencil icon for the dataset to edit its attributes
    • In the central panel, click Datatypes tab on the top
    • In the Assign Datatype, select smi from “New type” dropdown
      • Tip: you can start typing the datatype into the field to filter the dropdown menu
    • Click the Save button

Remove duplicated molecules

Hands-on: Remove duplicated molecules
  1. Remove duplicated molecules ( Galaxy version 3.1.1+galaxy0) with the following parameters:
    • “Molecular input file”: (output of Remove beginning )
    • “Select descriptor for molecule comparison”: Canonical SMILES
    Comment: short description

    For the downstream analysis deduplicated molecules are not required. Especially short, hybrid or uncompleted cluster can produce short molecular structures, that appear multiple times in an organisms. These structures can be regarded as artefacts and could probably be removed as well.

Generate fingerprints for the predicted secondary metabolites and the target database with Molecule to fingerprint

Various molecular fingerprint options can be used to convert the compounds. Details about molecular fingerprint can be found in Muegge and Mukherjee 2016 and Capecchi et al. 2020.

Hands-on: Task description
  1. Molecule to fingerprint ( Galaxy version 1.5) with the following parameters:
    • “Molecule file”: (output of Remove duplicated molecules )
    • “Type of fingerprint”: Open Babel FP2 fingerprints
  2. Molecule to fingerprint ( Galaxy version 1.5) with the following parameters:
    • “Molecule file”: output (MIBiG_compounds_3.0.sdf)
    • “Type of fingerprint”: Open Babel FP2 fingerprints
    Comment: Be consitent

    A major application of molecular fingerprints is to determine the similarity of compounds. For the downstream tool Similarity Search ( Galaxy version 0.2) it is important that the same fingerprint are used for the query and target compounds!

Now that we have converted our compounds into molecular fingerprints, we can compare them to find the closest match between our prediction and the target database.

Hands-on: Task description
  1. Similarity Search ( Galaxy version 0.2) with the following parameters:
    • “Subject database/sequences”: Chemfp fingerprint file
      • “Query Mode”: Query molecules are stores in a separate file
        • “Query molecules”: (output of Molecule to fingerprint for MIBiG_compounds_3.0.sdf )
        • “Target molecules”: (output of Molecule to fingerprint from Remove duplicated molecules )
      • “select the k nearest neighbors”: 1

Determine the novelty of the compounds using Natural Product likeness calculator

Normally, this tool allows to estimate how similar any kind of compound is to a natural product. In our case we know that the compounds are natural compounds. However, by comparing to a large source of known natural products we can estimate the novelty of our predicted structure. This could for example be used to mine metagenomic datasets for likely sources of uncharacterized molecular scaffolds.

Hands-on: Task description
  1. Natural Product ( Galaxy version 2.1) with the following parameters:
    • “Molecule file”: (output of Remove duplicated molecules )

Check Drug-likeness of the predicted compounds

Estimates the drug-likeness of molecules, based on eight commonly used molecular properties, and reports a score between 0 (all properties unfavourable) to 1 (all properties favourable). Two possible methods to weight the features are available (QEDw,mo, QEDw,max), as well as an option to leave features unweighted (QEDw,u).

The eight properties used are: molecular weight (MW), octanol–water partition coefficient (ALOGP), number of hydrogen bond donors (HBDs), number of hydrogen bond acceptors (HBAs), molecular polar surface area (PSA), number of rotatable bonds (ROTBs), number of aromatic rings (AROMs) and number of structural alerts (ALERTS).

Hands-on: Task description
  1. Drug-likeness ( Galaxy version 2021.03.4+galaxy0) with the following parameters:
    • “Molecule data in SDF or SMILES format”: (output of Remove duplicated molecules )

Conclusion

In this simple use case the combination of BGC prediction software and cheminformatics was used to detect and characterize novel secondary metabolites.