Metaproteomic and metagenomic analyses of defined oceanic microbial populations using microwave cell fixation and flow cytometric sorting

被引:11
|
作者
Mary, Isabelle [1 ,2 ]
Oliver, Anna [3 ]
Skipp, Paul [4 ]
Holland, Ross [2 ]
Topping, Juliette [2 ]
Tarran, Glen [5 ]
Scanlan, David J. [6 ]
O'Connor, C. David [4 ]
Whiteley, Andrew S. [3 ]
Burkill, Peter H. [7 ,8 ]
Zubkov, Mikhail V. [2 ]
机构
[1] Univ Blaise Pascal Clermont Ferrand II, Lab Microorganismes Genome & Environm, CNRS, UMR 6023, F-63177 Aubiere, France
[2] Natl Oceanog Ctr, Southampton, Hants, England
[3] CEH Oxford, Mol Microbial Ecol Sect, Biodivers & Ecosyst Funct Grp, Oxford, England
[4] Univ Southampton, Sch Biol Sci, Ctr Prote Res, Southampton, Hants, England
[5] Plymouth Marine Lab, Plymouth, Devon, England
[6] Univ Warwick, Dept Biol Sci, Coventry CV4 7AL, W Midlands, England
[7] Sir Alister Hardy Fdn Ocean Sci, Plymouth, Devon, England
[8] Univ Plymouth, Inst Marine, Plymouth PL4 8AA, Devon, England
关键词
high-speed cell sorting; microwave irradiation; protein sequencing; genome sequencing; oceanic cyanobacteria; microbial ecology; IN-SITU HYBRIDIZATION; SHOTGUN PROTEOMIC ANALYSIS; MARINE BACTERIOPLANKTON; OLIGONUCLEOTIDE PROBES; BACILLUS-SUBTILIS; SARGASSO SEA; COMMUNITIES; BACTERIA; ENUMERATION; PROTEINS;
D O I
10.1111/j.1574-6941.2010.00927.x
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
A major obstacle in the molecular investigation of natural, especially oceanic, microbial cells is their adequate preservation for further land-based molecular analyses. Here, we examined the use of microwaves for cell fixation before high-speed flow cytometric sorting to define the metaproteomes and metagenomes of key microbial populations. The microwave fixation procedure was established using cultures of Synechococcus cyanobacteria, the photosynthetic eukaryote Micromonas pusilla and the gammaproteobacterium Halomonas variabilis. Shotgun proteomic analyses showed that the profile of microwave-fixed and -unfixed Synechococcus sp. WH8102 cells was the same, and hence proteome identification of microwave-fixed sorted cells by nanoLC-MS/MS is possible. Microwave-fixed flow-sorted Synechococcus cells can also be successfully used for whole-genome amplification and fosmid library construction. We then carried out successful metaproteomic and metagenomic analyses of microwave-fixed Synechococcus cells flow sorted from concentrates of microbial cells, collected in the North Atlantic Ocean. Thus, the microwave fixation procedure developed appears to be useful for molecular studies of microbial populations in aquatic ecosystems.
引用
收藏
页码:10 / 18
页数:9
相关论文
共 41 条
  • [31] Studies of cell adhesion and flow cytometric analyses of degranulation, surface phenotype, and viability using human eosinophils, basophils, and mast cells
    Bochner, BS
    Sterbinsky, SA
    Saini, SA
    Columbo, M
    MacGlashan, DW
    METHODS, 1997, 13 (01) : 61 - 68
  • [32] FLOW CYTOMETRIC ANALYSIS OF RNA-CONTENT IN DIFFERENT CELL-POPULATIONS USING PYRONIN-Y AND METHYL GREEN
    POLLACK, A
    PRUDHOMME, DL
    GREENSTEIN, DB
    IRVIN, GL
    CLAFLIN, AJ
    BLOCK, NL
    CYTOMETRY, 1982, 3 (01): : 28 - 35
  • [33] The Identification and Enumeration of Dendritic Cell Populations from Individual Mouse Spleen and Peyer's Patches Using Flow Cytometric Analysis
    Duriancik, David A.
    Hoag, Kathleen A.
    CYTOMETRY PART A, 2009, 75A (11) : 951 - 959
  • [34] Development of Defined Microbial Population Standards Using Fluorescence Activated Cell Sorting for the Absolute Quantification of S. aureus Using Real-Time PCR
    Martinon, Alice
    Cronin, Ultan P.
    Wilkinson, Martin G.
    MOLECULAR BIOTECHNOLOGY, 2012, 50 (01) : 62 - 71
  • [35] Development of Defined Microbial Population Standards Using Fluorescence Activated Cell Sorting for the Absolute Quantification of S. aureus Using Real-Time PCR
    Alice Martinon
    Ultan P. Cronin
    Martin G. Wilkinson
    Molecular Biotechnology, 2012, 50 : 62 - 71
  • [36] Microbial characterisation of polyhydroxyalkanoates storing populations selected under different operating conditions using a cell-sorting RT-PCR approach
    Paulo C. Lemos
    Caterina Levantesi
    Luisa S. Serafim
    Simona Rossetti
    Maria A. M. Reis
    Valter Tandoi
    Applied Microbiology and Biotechnology, 2008, 78 : 351 - 360
  • [37] Microbial characterisation of polyhydroxyalkanoates storing populations selected under different operating conditions using a cell-sorting RT-PCR approach
    Lemos, Paulo C.
    Levantesi, Caterina
    Serafim, Luisa S.
    Rossetti, Simona
    Reis, Maria A. M.
    Tandoi, Valter
    APPLIED MICROBIOLOGY AND BIOTECHNOLOGY, 2008, 78 (02) : 351 - 360
  • [38] Psychedelics Produce Complex And Heterogeneous Transcriptional Responses In Diverse Cortical Cell Types In The Brain Of Rats As Determined By New Flow Cytometric Methods Allowing For Sorting Of Distinct Cell And Neuronal Populations From Whole Brain
    Martin, David
    Porretta, Connie
    Nichols, Charles D.
    FASEB JOURNAL, 2016, 30
  • [39] Generation of a NES-mScarlet Red Fluorescent Reporter Human iPSC Line for Live Cell Imaging and Flow Cytometric Analysis and Sorting Using CRISPR-Cas9-Mediated Gene Editing
    Nouri, Parivash
    Zimmer, Anja
    Brueggemann, Stefanie
    Friedrich, Robin
    Kuehn, Ralf
    Prakash, Nilima
    CELLS, 2022, 11 (02)
  • [40] Flow cytometric discrimination of mesenchymal progenitor cells from bone marrow-adherent cell populations using CD34/44/45(-) and Sca-1(+) markers
    Hachisuka, Hiroki
    Mochizuki, Yu
    Yasunaga, Yuji
    Natsu, Koji
    Sharman, Patrick
    Shinomiya, Rikuo
    Ochi, Mitsuo
    JOURNAL OF ORTHOPAEDIC SCIENCE, 2007, 12 (02) : 161 - 169