Cargando…

RetSynth: determining all optimal and sub-optimal synthetic pathways that facilitate synthesis of target compounds in chassis organisms

BACKGROUND: The efficient biological production of industrially and economically important compounds is a challenging problem. Brute-force determination of the optimal pathways to efficient production of a target chemical in a chassis organism is computationally intractable. Many current methods pro...

Descripción completa

Detalles Bibliográficos
Autores principales: Whitmore, Leanne S., Nguyen, Bernard, Pinar, Ali, George, Anthe, Hudson, Corey M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6734243/
https://www.ncbi.nlm.nih.gov/pubmed/31500573
http://dx.doi.org/10.1186/s12859-019-3025-9
_version_ 1783450112049020928
author Whitmore, Leanne S.
Nguyen, Bernard
Pinar, Ali
George, Anthe
Hudson, Corey M.
author_facet Whitmore, Leanne S.
Nguyen, Bernard
Pinar, Ali
George, Anthe
Hudson, Corey M.
author_sort Whitmore, Leanne S.
collection PubMed
description BACKGROUND: The efficient biological production of industrially and economically important compounds is a challenging problem. Brute-force determination of the optimal pathways to efficient production of a target chemical in a chassis organism is computationally intractable. Many current methods provide a single solution to this problem, but fail to provide all optimal pathways, optional sub-optimal solutions or hybrid biological/non-biological solutions. RESULTS: Here we present RetSynth, software with a novel algorithm for determining all optimal biological pathways given a starting biological chassis and target chemical. By dynamically selecting constraints, the number of potential pathways scales by the number of fully independent pathways and not by the number of overall reactions or size of the metabolic network. This feature allows all optimal pathways to be determined for a large number of chemicals and for a large corpus of potential chassis organisms. Additionally, this software contains other features including the ability to collect data from metabolic repositories, perform flux balance analysis, and to view optimal pathways identified by our algorithm using a built-in visualization module. This software also identifies sub-optimal pathways and allows incorporation of non-biological chemical reactions, which may be performed after metabolic production of precursor molecules. CONCLUSIONS: The novel algorithm designed for RetSynth streamlines an arduous and complex process in metabolic engineering. Our stand-alone software allows the identification of candidate optimal and additional sub-optimal pathways, and provides the user with necessary ranking criteria such as target yield to decide which route to select for target production. Furthermore, the ability to incorporate non-biological reactions into the final steps allows determination of pathways to production for targets that cannot be solely produced biologically. With this comprehensive suite of features RetSynth exceeds any open-source software or webservice currently available for identifying optimal pathways for target production. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12859-019-3025-9) contains supplementary material, which is available to authorized users.
format Online
Article
Text
id pubmed-6734243
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-67342432019-09-12 RetSynth: determining all optimal and sub-optimal synthetic pathways that facilitate synthesis of target compounds in chassis organisms Whitmore, Leanne S. Nguyen, Bernard Pinar, Ali George, Anthe Hudson, Corey M. BMC Bioinformatics Software BACKGROUND: The efficient biological production of industrially and economically important compounds is a challenging problem. Brute-force determination of the optimal pathways to efficient production of a target chemical in a chassis organism is computationally intractable. Many current methods provide a single solution to this problem, but fail to provide all optimal pathways, optional sub-optimal solutions or hybrid biological/non-biological solutions. RESULTS: Here we present RetSynth, software with a novel algorithm for determining all optimal biological pathways given a starting biological chassis and target chemical. By dynamically selecting constraints, the number of potential pathways scales by the number of fully independent pathways and not by the number of overall reactions or size of the metabolic network. This feature allows all optimal pathways to be determined for a large number of chemicals and for a large corpus of potential chassis organisms. Additionally, this software contains other features including the ability to collect data from metabolic repositories, perform flux balance analysis, and to view optimal pathways identified by our algorithm using a built-in visualization module. This software also identifies sub-optimal pathways and allows incorporation of non-biological chemical reactions, which may be performed after metabolic production of precursor molecules. CONCLUSIONS: The novel algorithm designed for RetSynth streamlines an arduous and complex process in metabolic engineering. Our stand-alone software allows the identification of candidate optimal and additional sub-optimal pathways, and provides the user with necessary ranking criteria such as target yield to decide which route to select for target production. Furthermore, the ability to incorporate non-biological reactions into the final steps allows determination of pathways to production for targets that cannot be solely produced biologically. With this comprehensive suite of features RetSynth exceeds any open-source software or webservice currently available for identifying optimal pathways for target production. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12859-019-3025-9) contains supplementary material, which is available to authorized users. BioMed Central 2019-09-09 /pmc/articles/PMC6734243/ /pubmed/31500573 http://dx.doi.org/10.1186/s12859-019-3025-9 Text en © The Author(s) 2019 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License(http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver(http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Software
Whitmore, Leanne S.
Nguyen, Bernard
Pinar, Ali
George, Anthe
Hudson, Corey M.
RetSynth: determining all optimal and sub-optimal synthetic pathways that facilitate synthesis of target compounds in chassis organisms
title RetSynth: determining all optimal and sub-optimal synthetic pathways that facilitate synthesis of target compounds in chassis organisms
title_full RetSynth: determining all optimal and sub-optimal synthetic pathways that facilitate synthesis of target compounds in chassis organisms
title_fullStr RetSynth: determining all optimal and sub-optimal synthetic pathways that facilitate synthesis of target compounds in chassis organisms
title_full_unstemmed RetSynth: determining all optimal and sub-optimal synthetic pathways that facilitate synthesis of target compounds in chassis organisms
title_short RetSynth: determining all optimal and sub-optimal synthetic pathways that facilitate synthesis of target compounds in chassis organisms
title_sort retsynth: determining all optimal and sub-optimal synthetic pathways that facilitate synthesis of target compounds in chassis organisms
topic Software
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6734243/
https://www.ncbi.nlm.nih.gov/pubmed/31500573
http://dx.doi.org/10.1186/s12859-019-3025-9
work_keys_str_mv AT whitmoreleannes retsynthdeterminingalloptimalandsuboptimalsyntheticpathwaysthatfacilitatesynthesisoftargetcompoundsinchassisorganisms
AT nguyenbernard retsynthdeterminingalloptimalandsuboptimalsyntheticpathwaysthatfacilitatesynthesisoftargetcompoundsinchassisorganisms
AT pinarali retsynthdeterminingalloptimalandsuboptimalsyntheticpathwaysthatfacilitatesynthesisoftargetcompoundsinchassisorganisms
AT georgeanthe retsynthdeterminingalloptimalandsuboptimalsyntheticpathwaysthatfacilitatesynthesisoftargetcompoundsinchassisorganisms
AT hudsoncoreym retsynthdeterminingalloptimalandsuboptimalsyntheticpathwaysthatfacilitatesynthesisoftargetcompoundsinchassisorganisms