期刊论文详细信息
BMC Biotechnology
Screening and genetic characterization of thermo-tolerant Synechocystis sp. PCC6803 strains created by adaptive evolution
Marcus Frohme1  Ulf Dühring2  Philipp Franke1  Nick Wolter1  Ulrich M Tillich3 
[1]Molecular Biotechnology and Functional Genomics, Technical University of Applied Sciences Wildau, Bahnhofstraße 1, 16-2001, D-15745 Wildau, Germany
[2]Algenol Biofuels Germany GmbH, Berlin, Germany
[3]Institute of Biology, Humboldt-University Berlin, Berlin, Germany
关键词: Adaptive evolution;    NGS;    HTS;    Thermal tolerance;    Synechocystis;    Cyanobacteria;   
Others  :  1084943
DOI  :  10.1186/1472-6750-14-66
 received in 2014-03-17, accepted in 2014-07-10,  发布年份 2014
PDF
【 摘 要 】

Background

Temperature tolerance is an important aspect for commercial scale outdoor cultivation of microalgae and cyanobacteria. While various genes are known to be related to Synechocystis sp. PCC6803's heat shock response, there is very limited published data concerning the specific genes involved in long term thermal tolerance. We have previously used random mutagenesis and adaptive evolution to generate a mixture of strains of Synechocystis sp. PCC6803 with significantly increased thermal tolerance. The genetic modifications leading to the phenotypes of the newly generated strains are the focus of this work.

Results

We used a custom screening platform, based on 96-deepwell microplate culturing in an in house designed cultivation chamber integrated in a liquid handling robot for screening and selection; in addition we also used a more conventional system. The increased thermal tolerances of the isolated monoclonal strains were validated in larger bioreactors and their whole genomes sequenced. Comparison of the sequence information to the parental wild type identified various mutations responsible for the enhanced phenotypes. Among the affected genes identified are clpC, pnp, pyk2, sigF, nlpD, pyrR, pilJ and cya1.

Conclusions

The applied methods (random mutagenesis, in vivo selection, screening, validation, whole genome sequencing) were successfully applied to identify various mutations, some of which are very unlikely to have been identified by other approaches. Several of the identified mutations are found in various strains and (due to their distribution) are likely to have occurred independently. This, coupled with the relatively low number of affected genes underscores the significance of these specific mutations to convey thermal tolerance in Synechocystis.

【 授权许可】

   
2014 Tillich et al.; licensee BioMed Central Ltd.

【 预 览 】
附件列表
Files Size Format View
20150113165518695.pdf 382KB PDF download
Figure 2. 42KB Image download
Figure 1. 26KB Image download
【 图 表 】

Figure 1.

Figure 2.

【 参考文献 】
  • [1]Mascarelli AL: Gold rush for algae. Nature 2009, 461:460-461.
  • [2]Savage PE, Hestekin JA: A perspective on algae, the environment, and energy. Environ Progr Sustain Energ 2013, 32:877-883.
  • [3]Haag AL: Algae bloom again. Nature 2007, 447:520-521.
  • [4]Waltz E: Biotech’s green gold? Nat Biotechnol 2009, 27:15-18.
  • [5]Jia K, Zhang Y: Systematic engineering of microorganisms to improve alcohol tolerance. Engineering in Life Sci 2010, 10:422-429.
  • [6]Miller J: Mutagenic specificity of ultraviolet light. J Mol Biol 1985, 182:45-65.
  • [7]Todd P, Monti-Bragadin C: MMS mutagenesis in strains of Escherichia coli carrying the R46 mutagenic enhancing plasmid: phenotypic analysis of Arg + revertants. Mech Mutagen 1979, 62:227-237.
  • [8]Tillich UM, Lehmann S, Schulze K, Dühring U, Frohme M: The optimal mutagen dosage to induce point-mutations in synechocystis sp. PCC6803 and its application to promote temperature tolerance. PLoS One 2012, 7:e49467.
  • [9]Foster PL: In vivo mutagenesis. Methods Enzymol 1991, 204:114-125.
  • [10]Witkin EM: Ultraviolet mutagenesis and inducible DNA repair in Escherichia coli. Bacteriol Rev 1976, 40:869-907.
  • [11]Shevell D, Friedman B: Resistance to alkylation damage in Escherichia coli: role of the Ada protein in induction of the adaptive response. Mutat Res 1990, 233:53-72.
  • [12]Griese M, Lange C, Soppa J: Ploidy in cyanobacteria. FEMS Microbiol Lett 2011, 323:124-131.
  • [13]Nakamoto H, Suzuki M, Kojima K: Targeted inactivation of the hrcA repressor gene in cyanobacteria. FEBS Lett 2003, 549:57-62.
  • [14]Suzuki I, Kanesaki Y, Hayashi H, Hall JJ, Simon WJ, Slabas AR, Murata N: The histidine kinase Hik34 is involved in thermotolerance by regulating the expression of heat shock genes in synechocystis. Plant Physiol 2005, 138:1409-1421.
  • [15]Rowland JG, Pang X, Suzuki I, Murata N, Simon WJ, Slabas AR: Identification of components associated with thermal acclimation of photosystem II in synechocystis sp. PCC6803. PLoS One 2010, 5:e10511.
  • [16]Suzuki I, Simon WJ, Slabas AR: The heat shock response of Synechocystis sp. PCC 6803 analysed by transcriptomics and proteomics. J Exp Bot 2006, 57:1573-1578.
  • [17]Inoue N, Taira Y, Emi T, Yamane Y, Kashino Y, Koike H, Satoh K: Acclimation to the growth temperature and the high-temperature effects on photosystem II and plasma membranes in a mesophilic cyanobacterium, synechocystis sp. PCC6803. Plant Cell Physiol 2001, 42:1140-1148.
  • [18]Mamedov M, Hayashi H, Murata N: Effects of glycinebetaine and unsaturation of membrane lipids on heat stability of photosynthetic electron-transport and phosphorylation reactions in Synechocystis PCC6803. Biochim Biophys Acta Bioenerg 1993, 1142:1-5.
  • [19]Kaneko T, Sato S, Kotani H, Tanaka A, Asamizu E, Nakamura Y, Miyajima N, Hirosawa M, Sugiura M, Sasamoto S, Kimura T, Hosouchi T, Matsuno A, Muraki A, Nakazaki N, Naruo K, Okumura S, Shimpo S, Takeuchi C, Wada T, Watanabe A, Yamada M, Yasuda M, Tabata S: Sequence analysis of the genome of the unicellular cyanobacterium synechocystis sp. Strain PCC6803. II. Sequence determination of the entire genome and assignment of potential protein-coding regions (supplement). DNA Res: Int J for rapid Pub of reports on genes and Genom 1996, 3:185-209.
  • [20]Glenn TC: Field guide to next-generation DNA sequencers: FIELD GUIDE TO NEXT-GEN SEQUENCERS. Mol Ecol Resour 2011, 11:759-769.
  • [21]Loman NJ, Constantinidou C, Chan JZ, Halachev M, Sergeant M, Penn CW, Robinson ER, Pallen MJ: High-throughput bacterial genome sequencing: an embarrassment of choice, a world of opportunity. Nat Rev Microbiol 2012, 10:599-606.
  • [22]Jünemann S, Sedlazeck FJ, Prior K, Albersmeier A, John U, Kalinowski J, Mellmann A, Goesmann A, von Haeseler A, Stoye J: Updating benchtop sequencing performance comparison. Nat Biotechnol 2013, 31:294-296.
  • [23]Suzuki S, Ono N, Furusawa C, Ying B-W, Yomo T: Comparison of sequence reads obtained from three next-generation sequencing platforms. PLoS One 2011, 6:e19534.
  • [24]Quail MA, Smith M, Coupland P, Otto TD, Harris SR, Connor TR, Bertoni A, Swerdlow HP, Gu Y: A tale of three next generation sequencing platforms: comparison of Ion torrent, pacific biosciences and illumina MiSeq sequencers. BMC Genomics 2012, 13:341.
  • [25]Marin K, Kanesaki Y, Los D, Murata N: Gene expression profiling reflects physiological processes in salt acclimation of Synechocystis sp. strain PCC 6803. Plant \ldots 2004, 136:3290-3300.
  • [26]Huang L, McCluskey M: Global gene expression profiles of the cyanobacterium Synechocystis sp. strain PCC 6803 in response to irradiation with UV-B and white light. J of \ldots 2002, 184:6845-6858.
  • [27]Kurian D, Phadwal K, Mäenpää P: Proteomic characterization of acid stress response in Synechocystis sp. PCC 6803. Proteomics 2006, 6:3614-3624.
  • [28]Rowland JG, Simon WJ, Prakash JSS, Slabas AR: Proteomics reveals a role for the RNA helicase crhR in the modulation of multiple metabolic pathways during cold acclimation of Synechocystis sp. PCC6803. J Proteome Res 2011, 10:3674-3689.
  • [29]Huckauf J, Nomura C, Forchhammer K, Hagemann M: Stress responses of Synechocystis sp. strain PCC 6803 mutants impaired in genes encoding putative alternative sigma factors. Microbiol (Reading, England) 2000, 146(Pt 1):2877-2889.
  • [30]Barker M, de Vries R, Nield J, Komenda J, Nixon PJ: The deg proteases protect Synechocystis sp. PCC 6803 during heat and light stresses but are not essential for removal of damaged D1 protein during the photosystem two repair cycle. The J of Biol Chem 2006, 281:30347-30355.
  • [31]Bhaya D, Watanabe N, Ogawa T, Grossman AR: The role of an alternative sigma factor in motility and pilus formation in the cyanobacterium Synechocystis sp. strain PCC6803. Proc Natl Acad Sci U S A 1999, 96:3188-3193.
  • [32]Asayama M, Imamura S: Stringent promoter recognition and autoregulation by the group 3 sigma-factor SigF in the cyanobacterium Synechocystis sp. strain PCC 6803. Nucleic Acids Res 2008, 36:5297-5305.
  • [33]Chung YH, Cho MS, Moon YJ, Choi JS, Yoo YC, Park YI, Lee KM, Kang KW, Park YM: ctr1, a gene involved in a signal transduction pathway of the gliding motility in the cyanobacterium Synechocystis sp. PCC 6803. FEBS Lett 2001, 492:33-38.
  • [34]Knowles VL, Plaxton WC: From genome to enzyme: analysis of Key glycolytic and oxidative pentose-phosphate pathway enzymes in the cyanobacterium synechocystis sp. PCC 6803. Plant Cell Physiol 2003, 44:758-763.
  • [35]Lange R, Hengge-Aronis R: The nIpD gene is located in an operon with rpoS on the Escherichia coli chromosome and encodes a novel lipoprotein with a potential function in ceil wall formation. Mol Microbiol 1994, 13:733-743.
  • [36]Uehara T, Parzych KR, Dinh T, Bernhardt TG: Daughter cell separation is controlled by cytokinetic ring-activated cell wall hydrolysis. EMBO J 2010, 29:1412-1422.
  • [37]Uehara T, Dinh T, Bernhardt TG: LytM-domain factors Are required for daughter cell separation and rapid ampicillin-induced lysis in Escherichia coli. J Bacteriol 2009, 191:5094-5107.
  • [38]Domain F, Houot L, Chauvat F, Cassier-Chauvat C: Function and regulation of the cyanobacterial genes lexA, recA and ruvB: LexA is critical to the survival of cells facing inorganic carbon starvation. Mol Microbiol 2004, 53:65-80.
  • [39]Koropatkin NM, Koppenaal DW, Pakrasi HB, Smith TJ: The structure of a cyanobacterial bicarbonate transport protein, CmpA. J Biol Chem 2007, 282:2606-2614.
  • [40]Trautmann D, Voss B, Wilde A, Al-Babili S, Hess WR: Microevolution in cyanobacteria: Re-sequencing a motile substrain of synechocystis sp. PCC 6803. DNA Res 2012, 19:435-448.
  • [41]Alper H, Fischer C, Nevoigt E, Stephanopoulos G: Tuning genetic control through promoter engineering. PNAS 2005, 102:12678-12683.
  • [42]Bhaya D, Nakasugi K, Fazeli F, Burriesci MS: Phototaxis and impaired motility in adenylyl cyclase and cyclase receptor protein mutants of Synechocystis sp. strain PCC 6803. J Bacteriol 2006, 188:7306-7310.
  • [43]Terauchi K, Ohmori M: An adenylate cyclase, Cya1, regulates cell motility in the cyanobacterium Synechocystis sp. PCC 6803. Plant Cell Physiol 1999, 40:248-251.
  • [44]Andrade MA, Bork P: HEAT repeats in the Huntington’s disease protein. Nat Genet 1995, 11:115-116.
  • [45]Groves MR, Hanlon N, Turowski P, Hemmings BA, Barford D: The structure of the protein phosphatase 2A PR65/a subunit reveals the conformation of its 15 tandemly repeated HEAT motifs. Cell 1999, 96:99-110.
  • [46]Tcherkez GGB, Farquhar GD, Andrews TJ: Despite slow catalysis and confused substrate specificity, all ribulose bisphosphate carboxylases may be nearly perfectly optimized. Proc Natl Acad Sci U S A 2006, 103:7246-7251.
  • [47]Ratkowsky DA, Olley J, McMeekin TA, Ball A: Relationship between temperature and growth rate of bacterial cultures. J Bacteriol 1982, 149:1-5.
  • [48]Zwietering MH, de Koos JT, Hasenack BE, de Witt JC, van’t Riet K: Modeling of bacterial growth as a function of temperature. Appl Environ Microbiol 1991, 57:1094-1101.
  • [49]Franche C, Damerval T: Tests on nif probes and DNA hybridizations. In Methods in Enzymology Edited by Lester Packer ANG Academic Press. 1988, 803-808. Volume 167
  • [50]Roche GS Reference Mapper http://www.454.com/products/analysis-software/ webcite
  • [51]Cingolani P, Platts A, Coon M, Nguyen T, Wang L, Land SJ, Lu X, Ruden DM: A program for annotating and predicting the effects of single nucleotide polymorphisms, SnpEff: SNPs in the genome of Drosophila melanogaster strain w1118; iso-2; iso-3. Fly 2012, 6:80-92.
  • [52]115fx: UT's Github Repository for NGS Skripts. https://github.com/utillich/NGS_Scripts webcite
  • [53]CyanoBase Synechocystis gene categories http://genome.microbedb.jp/cyanobase/Synechocystis/genes/category.csv webcite
  • [54]Milne I, Bayer M, Cardle L, Shaw P, Stephen G, Wright F, Marshall D: Tablet–next generation sequence assembly visualization. Bioinformatics 2010, 26:401-402.
  • [55]FinchTV 1.31 http://www.geospiza.com webcite
  • [56]Marshall OJ: PerlPrimer: cross-platform, graphical primer design for standard, bisulphite and real-time PCR. Bioinformatics 2004, 20:2471-2472.
  文献评价指标  
  下载次数:16次 浏览次数:9次