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A genomic perspective on the potential of Actinobacillus succinogenes for industrial succinate production

BACKGROUND: Succinate is produced petrochemically from maleic anhydride to satisfy a small specialty chemical market. If succinate could be produced fermentatively at a price competitive with that of maleic anhydride, though, it could replace maleic anhydride as the precursor of many bulk chemicals,...

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Autores principales: McKinlay, James B, Laivenieks, Maris, Schindler, Bryan D, McKinlay, Anastasia A, Siddaramappa, Shivakumara, Challacombe, Jean F, Lowry, Stephen R, Clum, Alicia, Lapidus, Alla L, Burkhart, Kirk B, Harkins, Victoria, Vieille, Claire
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3091790/
https://www.ncbi.nlm.nih.gov/pubmed/21118570
http://dx.doi.org/10.1186/1471-2164-11-680
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author McKinlay, James B
Laivenieks, Maris
Schindler, Bryan D
McKinlay, Anastasia A
Siddaramappa, Shivakumara
Challacombe, Jean F
Lowry, Stephen R
Clum, Alicia
Lapidus, Alla L
Burkhart, Kirk B
Harkins, Victoria
Vieille, Claire
author_facet McKinlay, James B
Laivenieks, Maris
Schindler, Bryan D
McKinlay, Anastasia A
Siddaramappa, Shivakumara
Challacombe, Jean F
Lowry, Stephen R
Clum, Alicia
Lapidus, Alla L
Burkhart, Kirk B
Harkins, Victoria
Vieille, Claire
author_sort McKinlay, James B
collection PubMed
description BACKGROUND: Succinate is produced petrochemically from maleic anhydride to satisfy a small specialty chemical market. If succinate could be produced fermentatively at a price competitive with that of maleic anhydride, though, it could replace maleic anhydride as the precursor of many bulk chemicals, transforming a multi-billion dollar petrochemical market into one based on renewable resources. Actinobacillus succinogenes naturally converts sugars and CO(2 )into high concentrations of succinic acid as part of a mixed-acid fermentation. Efforts are ongoing to maximize carbon flux to succinate to achieve an industrial process. RESULTS: Described here is the 2.3 Mb A. succinogenes genome sequence with emphasis on A. succinogenes's potential for genetic engineering, its metabolic attributes and capabilities, and its lack of pathogenicity. The genome sequence contains 1,690 DNA uptake signal sequence repeats and a nearly complete set of natural competence proteins, suggesting that A. succinogenes is capable of natural transformation. A. succinogenes lacks a complete tricarboxylic acid cycle as well as a glyoxylate pathway, and it appears to be able to transport and degrade about twenty different carbohydrates. The genomes of A. succinogenes and its closest known relative, Mannheimia succiniciproducens, were compared for the presence of known Pasteurellaceae virulence factors. Both species appear to lack the virulence traits of toxin production, sialic acid and choline incorporation into lipopolysaccharide, and utilization of hemoglobin and transferrin as iron sources. Perspectives are also given on the conservation of A. succinogenes genomic features in other sequenced Pasteurellaceae. CONCLUSIONS: Both A. succinogenes and M. succiniciproducens genome sequences lack many of the virulence genes used by their pathogenic Pasteurellaceae relatives. The lack of pathogenicity of these two succinogens is an exciting prospect, because comparisons with pathogenic Pasteurellaceae could lead to a better understanding of Pasteurellaceae virulence. The fact that the A. succinogenes genome encodes uptake and degradation pathways for a variety of carbohydrates reflects the variety of carbohydrate substrates available in the rumen, A. succinogenes's natural habitat. It also suggests that many different carbon sources can be used as feedstock for succinate production by A. succinogenes.
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spelling pubmed-30917902011-05-11 A genomic perspective on the potential of Actinobacillus succinogenes for industrial succinate production McKinlay, James B Laivenieks, Maris Schindler, Bryan D McKinlay, Anastasia A Siddaramappa, Shivakumara Challacombe, Jean F Lowry, Stephen R Clum, Alicia Lapidus, Alla L Burkhart, Kirk B Harkins, Victoria Vieille, Claire BMC Genomics Research Article BACKGROUND: Succinate is produced petrochemically from maleic anhydride to satisfy a small specialty chemical market. If succinate could be produced fermentatively at a price competitive with that of maleic anhydride, though, it could replace maleic anhydride as the precursor of many bulk chemicals, transforming a multi-billion dollar petrochemical market into one based on renewable resources. Actinobacillus succinogenes naturally converts sugars and CO(2 )into high concentrations of succinic acid as part of a mixed-acid fermentation. Efforts are ongoing to maximize carbon flux to succinate to achieve an industrial process. RESULTS: Described here is the 2.3 Mb A. succinogenes genome sequence with emphasis on A. succinogenes's potential for genetic engineering, its metabolic attributes and capabilities, and its lack of pathogenicity. The genome sequence contains 1,690 DNA uptake signal sequence repeats and a nearly complete set of natural competence proteins, suggesting that A. succinogenes is capable of natural transformation. A. succinogenes lacks a complete tricarboxylic acid cycle as well as a glyoxylate pathway, and it appears to be able to transport and degrade about twenty different carbohydrates. The genomes of A. succinogenes and its closest known relative, Mannheimia succiniciproducens, were compared for the presence of known Pasteurellaceae virulence factors. Both species appear to lack the virulence traits of toxin production, sialic acid and choline incorporation into lipopolysaccharide, and utilization of hemoglobin and transferrin as iron sources. Perspectives are also given on the conservation of A. succinogenes genomic features in other sequenced Pasteurellaceae. CONCLUSIONS: Both A. succinogenes and M. succiniciproducens genome sequences lack many of the virulence genes used by their pathogenic Pasteurellaceae relatives. The lack of pathogenicity of these two succinogens is an exciting prospect, because comparisons with pathogenic Pasteurellaceae could lead to a better understanding of Pasteurellaceae virulence. The fact that the A. succinogenes genome encodes uptake and degradation pathways for a variety of carbohydrates reflects the variety of carbohydrate substrates available in the rumen, A. succinogenes's natural habitat. It also suggests that many different carbon sources can be used as feedstock for succinate production by A. succinogenes. BioMed Central 2010-11-30 /pmc/articles/PMC3091790/ /pubmed/21118570 http://dx.doi.org/10.1186/1471-2164-11-680 Text en Copyright ©2010 McKinlay et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
McKinlay, James B
Laivenieks, Maris
Schindler, Bryan D
McKinlay, Anastasia A
Siddaramappa, Shivakumara
Challacombe, Jean F
Lowry, Stephen R
Clum, Alicia
Lapidus, Alla L
Burkhart, Kirk B
Harkins, Victoria
Vieille, Claire
A genomic perspective on the potential of Actinobacillus succinogenes for industrial succinate production
title A genomic perspective on the potential of Actinobacillus succinogenes for industrial succinate production
title_full A genomic perspective on the potential of Actinobacillus succinogenes for industrial succinate production
title_fullStr A genomic perspective on the potential of Actinobacillus succinogenes for industrial succinate production
title_full_unstemmed A genomic perspective on the potential of Actinobacillus succinogenes for industrial succinate production
title_short A genomic perspective on the potential of Actinobacillus succinogenes for industrial succinate production
title_sort genomic perspective on the potential of actinobacillus succinogenes for industrial succinate production
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3091790/
https://www.ncbi.nlm.nih.gov/pubmed/21118570
http://dx.doi.org/10.1186/1471-2164-11-680
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