Integrated lysis procedures reduce extraction biases of microbial DNA from mangrove sediment

被引:15
作者
Jiang, Yun-Xia [1 ]
Wu, Ji-Guo [1 ]
Yu, Ke-Qiang [2 ]
Ai, Chun-Xiang [3 ]
Zou, Fei [1 ]
Zhou, Hong-Wei [1 ]
机构
[1] So Med Univ, Dept Environm Hlth, Sch Publ Hlth & Trop Med, Guangzhou 510515, Guangdong, Peoples R China
[2] So Med Univ, Sch Tradit Chinese Med, Guangzhou 510515, Guangdong, Peoples R China
[3] Xiamen Univ, Dept Marine Technol & Ocean Engn, Coll Oceanog & Environm Sci, Xiamen 361005, Peoples R China
关键词
DNA extraction; DNA quality; Denaturing gradient gel electrophoresis (DGGE); Microbial community structure; GRADIENT GEL-ELECTROPHORESIS; COMMUNITY STRUCTURE; SOIL; DGGE; DIVERSITY;
D O I
10.1016/j.jbiosc.2010.10.006
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Sufficient lysis of soil or sediment microbes is a critical step for analyzing microbial community structures and for preparing metagenomic DNA libraries. The present study compared lysis methods for recovering archaeal, bacterial, actinomycete, and fungal DNAs from a mangrove sediment sample. PCR results showed that individual procedures using SDS, lysozyme, sonication, freeze-thaw, microwave, and vigorous shaking could extract archaeal or bacterial DNA but failed for actinomycetes or fungi cells. In comparison, an integrated lysis procedure using SDS, lysozyme, and vigorous,shaking successfully obtained fungal DNA, and a combination of SDS, lysozyme, vigorous shaking, and microwave treatments recovered DNA from actinomycetes. Denaturing gradient gel electrophoresis (DGGE) results showed that although single lysis procedures can lyse bacterial DNA, all of them assessed the indigenous bacterial community structure with significant biases. The integrated lysis protocols described in the present study could be useful for extracting DNA from various types of sediments. (C) 2010, The Society for Biotechnology, Japan. All rights reserved.
引用
收藏
页码:153 / 157
页数:5
相关论文
共 21 条
  • [1] Anderson IC, 2003, ENVIRON MICROBIOL, V5, P1121, DOI [10.1046/j.1462-2920.2003.00522.x, 10.1046/j.1462-2920.2003.00383.x]
  • [2] PCR-DGGE Comparison of Bacterial Community Structure in Fresh and Archived Soils Sampled along a Chihuahuan Desert Elevational Gradient
    Campbell, James H.
    Clark, Jeb S.
    Zak, John C.
    [J]. MICROBIAL ECOLOGY, 2009, 57 (02) : 261 - 266
  • [3] DNA extraction method affects microbial community profiles from soils and sediment
    Carrigg, Cora
    Rice, Olivia
    Kavanagh, Siobhan
    Collins, Gavin
    O'Flaherty, Vincent
    [J]. APPLIED MICROBIOLOGY AND BIOTECHNOLOGY, 2007, 77 (04) : 955 - 964
  • [4] Identification of and spatio-temporal differences between microbial assemblages from two neighboring sulfurous lakes:: Comparison by microscopy and denaturing gradient gel electrophoresis
    Casamayor, EO
    Schäfer, H
    Bañeras, L
    Pedrós-Alió, C
    Muyzer, G
    [J]. APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 2000, 66 (02) : 499 - 508
  • [5] ARCHAEA IN COASTAL MARINE ENVIRONMENTS
    DELONG, EF
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1992, 89 (12) : 5685 - 5689
  • [6] Frostegård Å, 1999, APPL ENVIRON MICROB, V65, P5409
  • [7] Molecular biological access to the chemistry of unknown soil microbes: A new frontier for natural products
    Handelsman, J
    Rondon, MR
    Brady, SF
    Clardy, J
    Goodman, RM
    [J]. CHEMISTRY & BIOLOGY, 1998, 5 (10): : R245 - R249
  • [8] THE 23S RIBOSOMAL-RNA HIGHER-ORDER STRUCTURE OF PSEUDOMONAS-CEPACIA AND OTHER PROKARYOTES
    HOPFL, P
    LUDWIG, W
    SCHLEIFER, KH
    LARSEN, N
    [J]. EUROPEAN JOURNAL OF BIOCHEMISTRY, 1989, 185 (02): : 355 - 364
  • [9] DNA isolation from soil samples for cloning in different hosts
    Kauffmann, IM
    Schmitt, J
    Schmid, RD
    [J]. APPLIED MICROBIOLOGY AND BIOTECHNOLOGY, 2004, 64 (05) : 665 - 670
  • [10] Methods of studying soil microbial diversity
    Kirk, JL
    Beaudette, LA
    Hart, M
    Moutoglis, P
    Khironomos, JN
    Lee, H
    Trevors, JT
    [J]. JOURNAL OF MICROBIOLOGICAL METHODS, 2004, 58 (02) : 169 - 188