Abstract

There is a growing interest in the Non-ribosomal peptide synthetases (NRPSs) and polyketide synthases (PKSs) of microbes, fungi and plants because they can produce bioactive peptides such as antibiotics. The ability to identify the substrate specificity of the enzyme's adenylation (A) and acyl-transferase (AT) domains is essential to rationally deduce or engineer new products. We here report on a Hidden Markov Model (HMM)-based ensemble method to predict the substrate specificity at high quality. We collected a new reference set of experimentally validated sequences. An initial classification based on alignment and Neighbor Joining was performed in line with most of the previously published prediction methods. We then created and tested single substrate specific HMMs and found that their use improved the correct identification significantly for A as well as for AT domains. A major advantage of the use of HMMs is that it abolishes the dependency on multiple sequence alignment and residue selection that is hampering the alignment-based clustering methods. Using our models we obtained a high prediction quality for the substrate specificity of the A domains similar to two recently published tools that make use of HMMs or Support Vector Machines (NRPSsp and NRPS predictor2, respectively). Moreover, replacement of the single substrate specific HMMs by ensembles of models caused a clear increase in prediction quality. We argue that the superiority of the ensemble over the single model is caused by the way substrate specificity evolves for the studied systems. It is likely that this also holds true for other protein domains. The ensemble predictor has been implemented in a simple web-based tool that is available at http://www.cmbi.ru.nl/NRPS-PKS-substrate-predictor/.

Highlights

  • In recent years the Non-Ribosomal Peptide Synthetases (NRPSs) and PolyKetide Synthases (PKSs) have gained considerable interest as they can produce polypeptide- and polyketidebased secondary metabolites that exhibit important pharmaceutical and biological activities

  • The Synth(et)ases can be found in a wide variety of bacteria, fungi and plants, and produce secondary metabolites that range from antibiotics to kill competitors, to surfactants to thrive in a biofilm environment

  • The core domains are organized in functional modules and multiple modules make up a kind of assembly-line to construct linear, cyclic or branched secondary metabolites

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Summary

Introduction

In recent years the Non-Ribosomal Peptide Synthetases (NRPSs) and PolyKetide Synthases (PKSs) have gained considerable interest as they can produce polypeptide- and polyketidebased secondary metabolites that exhibit important pharmaceutical and biological activities (see e.g. [1,2,3,4,5,6,7]). In recent years the Non-Ribosomal Peptide Synthetases (NRPSs) and PolyKetide Synthases (PKSs) have gained considerable interest as they can produce polypeptide- and polyketidebased secondary metabolites that exhibit important pharmaceutical and biological activities The simplest NRPS module consists of at least three core domains: an adenylation domain (A) that selects, activates and loads the substrate (i.e. proteinogenic and non-proteinogenic amino acids); a thiolation domain (T) -which is known as the peptidyl carrier protein- that covalently attaches the substrate to the synthetase; and a condensation domain (C) that catalyzes peptide bond formation. NRPSs and PKSs have a fourth domain, the thio-esterase domain (TE) that releases the assembled polypeptide and polyketide chains from the synth(et)ase. These other enzymes are usually associated to the synth(et)ase complex and their genes are often organized in the same gene clusters [23]

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