BMC Systems Biology | |
Comparisons of Shewanella strains based on genome annotations, modeling, and experiments | |
Jennifer L Reed1  Margaret F Romine2  Margrethe H Serres3  Jenna M Llull1  Klaus N Lovendahl1  Trang T Vu1  Wai Kit Ong1  | |
[1] University of Wisconsin-Madison, Madison, USA;Pacific Northwest National Laboratory, Richland, USA;Marine Biological Laboratory, Woods Hole, USA | |
关键词: FBA; Phenotype; Electron acceptors; Constraint-based model; | |
Others : 866663 DOI : 10.1186/1752-0509-8-31 |
|
received in 2013-10-18, accepted in 2014-03-06, 发布年份 2014 | |
【 摘 要 】
Background
Shewanella is a genus of facultatively anaerobic, Gram-negative bacteria that have highly adaptable metabolism which allows them to thrive in diverse environments. This quality makes them an attractive bacterial target for research in bioremediation and microbial fuel cell applications. Constraint-based modeling is a useful tool for helping researchers gain insights into the metabolic capabilities of these bacteria. However, Shewanella oneidensis MR-1 is the only strain with a genome-scale metabolic model constructed out of 21 sequenced Shewanella strains.
Results
In this work, we updated the model for Shewanella oneidensis MR-1 and constructed metabolic models for three other strains, namely Shewanella sp. MR-4, Shewanella sp. W3-18-1, and Shewanella denitrificans OS217 which span the genus based on the number of genes lost in comparison to MR-1. We also constructed a Shewanella core model that contains the genes shared by all 21 sequenced strains and a few non-conserved genes associated with essential reactions. Model comparisons between the five constructed models were done at two levels – for wildtype strains under different growth conditions and for knockout mutants under the same growth condition. In the first level, growth/no-growth phenotypes were predicted by the models on various carbon sources and electron acceptors. Cluster analysis of these results revealed that the MR-1 model is most similar to the W3-18-1 model, followed by the MR-4 and OS217 models when considering predicted growth phenotypes. However, a cluster analysis done based on metabolic gene content revealed that the MR-4 and W3-18-1 models are the most similar, with the MR-1 and OS217 models being more distinct from these latter two strains. As a second level of comparison, we identified differences in reaction and gene content which give rise to different functional predictions of single and double gene knockout mutants using Comparison of Networks by Gene Alignment (CONGA). Here, we showed how CONGA can be used to find biomass, metabolic, and genetic differences between models.
Conclusions
We developed four strain-specific models and a general core model that can be used to do various in silico studies of Shewanella metabolism. The developed models provide a platform for a systematic investigation of Shewanella metabolism to aid researchers using Shewanella in various biotechnology applications.
【 授权许可】
2014 Ong et al.; licensee BioMed Central Ltd.
【 预 览 】
Files | Size | Format | View |
---|---|---|---|
20140727080713296.pdf | 926KB | download | |
36KB | Image | download | |
45KB | Image | download | |
43KB | Image | download | |
38KB | Image | download | |
182KB | Image | download |
【 图 表 】
【 参考文献 】
- [1]Nealson KH, Scott J: Ecophysiology of the Genus Shewanella. In Prokaryotes: A Handbook on the Biology of Bacteria, Vol 6. Third edition. New York, NY: Springer; 2006:1133-1151.
- [2]Fredrickson JK, Romine MF, Beliaev AS, Auchtung JM, Driscoll ME, Gardner TS, Nealson KH, Osterman AL, Pinchuk G, Reed JL, Rodionov DA, Rodrigues JLM, Saffarini DA, Serres MH, Spormann AM, Zhulin IB, Tiedje JM: Towards environmental systems biology of Shewanella. Nat Rev Microbiol 2008, 6:592-603.
- [3]Rodionov DA, Yang C, Li XQ, Rodionova IA, Wang YB, Obraztsova AY, Zagnitko OP, Overbeek R, Romine MF, Reed S, Fredrickson JK, Nealson KH, Osterman AL: Genomic encyclopedia of sugar utilization pathways in the Shewanella genus. BMC Genomics 2010, 11:494. BioMed Central Full Text
- [4]Deutschbauer A, Price MN, Wetmore KM, Shao WJ, Baumohl JK, Xu ZC, Nguyen M, Tamse R, Davis RW, Arkin AP: Evidence-based annotation of gene function in Shewanella oneidensis MR-1 using genome-wide fitness profiling across 121 conditions. Plos Genetics 2011, 7(11):e1002385.
- [5]Nealson KH, Belz A, McKee B: Breathing metals as a way of life: geobiology in action. Anton Leeuw Int J G 2002, 81:215-222.
- [6]Gorby YA, Lovley DR: Enzymatic uranium precipitation. Environ Sci Technol 1992, 26:205-207.
- [7]Hau HH, Gralnick JA: Ecology and biotechnology of the genus Shewanella. Annu Rev Microbiol 2007, 61:237-258.
- [8]Flynn JM, Ross DE, Hunt KA, Bond DR, Gralnick JA: Enabling unbalanced fermentations by using engineered electrode-interfaced bacteria. MBio 2010., 1doi: 10.1128/mBio.00190-10
- [9]Rodionov DA, Novichkov PS, Stavrovskaya ED, Rodionova IA, Li X, Kazanov MD, Ravcheev DA, Gerasimova AV, Kazakov AE, Kovaleva GY, Permina EA, Laikova ON, Overbeek R, Romine MF, Fredrickson JK, Arkin AP, Dubchak I, Osterman AL, Gelfand MS: Comparative genomic reconstruction of transcriptional networks controlling central metabolism in the Shewanella genus. BMC Genomics 2011, 12(Suppl 1):S3. BioMed Central Full Text
- [10]Rodrigues JL, Serres MH, Tiedje JM: Large-scale comparative phenotypic and genomic analyses reveal ecological preferences of shewanella species and identify metabolic pathways conserved at the genus level. Appl Environ Microbiol 2011, 77:5352-5360.
- [11]Pinchuk GE, Hill EA, Geydebrekht OV, De Ingeniis J, Zhang X, Osterman A, Scott JH, Reed SB, Romine MF, Konopka AE, Beliaev AS, Fredrickson JK, Reed JL: Constraint-based model of Shewanella oneidensis MR-1 metabolism: a tool for data analysis and hypothesis generation. PLoS Comput Biol 2010, 6:e1000822.
- [12]Vu TT, Stolyar SM, Pinchuk GE, Hill EA, Kucek LA, Brown RN, Lipton MS, Osterman A, Fredrickson JK, Konopka AE, Beliaev AS, Reed JL: Genome-scale modeling of light-driven reductant partitioning and carbon fluxes in diazotrophic unicellular cyanobacterium Cyanothece sp. ATCC 51142. PLoS Comput Biol 2012, 8:e1002460.
- [13]Kanehisa M, Goto S, Sato Y, Furumichi M, Tanabe M: KEGG for integration and interpretation of large-scale molecular data sets. Nucleic Acids Res 2012, 40:D109-D114.
- [14]Hamilton JJ, Reed JL: Identification of functional differences in metabolic networks using comparative genomics and constraint-based models. PLoS One 2012, 7:e34670.
- [15]Konstantinidis KT, Serres MH, Romine MF, Rodrigues JL, Auchtung J, McCue LA, Lipton MS, Obraztsova A, Giometti CS, Nealson KH, Fredrickson JK, Tiedje JM: Comparative systems biology across an evolutionary gradient within the Shewanella genus. Proc Natl Acad Sci USA 2009, 106:15909-15914.
- [16]Romine MF, Carlson TS, Norbeck AD, McCue LA, Lipton MS: Identification of mobile elements and pseudogenes in the Shewanella oneidensis MR-1 genome. Appl Environ Microbiol 2008, 74:3257-3265.
- [17]Romine MF: Genome-wide protein localization prediction strategies for gram negative bacteria. BMC Genomics 2011, 12(Suppl 1):S1. BioMed Central Full Text
- [18]Orth JD, Thiele I, Palsson BØ: What is flux balance analysis? Nat Biotechnol 2010, 28:245-248.
- [19]Vinogradov E, Korenevsky A, Beveridge TJ: The structure of the rough-type lipopolysaccharide from Shewanella oneidensis MR-1, containing 8-amino-8-deoxy-Kdo and an open-chain form of 2-acetamido-2-deoxy-D-galactose. Carbohydr Res 2003, 338:1991-1997.
- [20]Joyce AR, Reed JL, White A, Edwards R, Osterman A, Baba T, Mori H, Lesely SA, Palsson B, Agarwalla S: Experimental and computational assessment of conditionally essential genes in Escherichia coli. J Bacteriol 2006, 188:8259-8271.
- [21]Monk JM, Charusanti P, Aziz RK, Lerman JA, Premyodhin N, Orth JD, Feist AM, Palsson B: Genome-scale metabolic reconstructions of multiple Escherichia coli strains highlight strain-specific adaptations to nutritional environments. Proc Natl Acad Sci USA 2013, 110:20338-20343.