Development of new procedures for the isolation of phytoplankton DNA from fixed samples

被引:19
作者
Bertozzini, E
Penna, A
Pierboni, E
Bruce, I
Magnani, M
机构
[1] Univ Urbino, Inst Biol Chem G Fornaini, I-61029 Urbino, PU, Italy
[2] Univ Urbino, Ctr Biotechnol, I-61032 Fano, PU, Italy
[3] Univ Urbino, Ctr Biol Ambientale, I-61100 Pesaro, PU, Italy
[4] Ist Zooprofilatt Sperimentale Umbria & Marche, I-06126 Perugia, PG, Italy
[5] Univ Greenwich, Sch Chem & Life Sci, Chatham ME4 4TB, Kent, England
关键词
DNA extraction; fixatives; harmful algal blooms (HABs); magnetisable solid phase support (MSPS); PCR;
D O I
10.1007/s10811-005-2130-5
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
Phytoplankton samples collected for routine monitoring programmes have traditionally been preserved with fixatives before subsequent analytical procedures such as microscope-based identification, or simply to permit transport between laboratories. In recent years, to simplify identification and enumeration, the use of DNA or RNA probes coupled with the PCR assay has progressed and now represents a routine procedure for screening cultured and field samples. However, the phytoplankton cells have often still to be treated as fixed samples. The extraction of genomic DNA from fixed cultures of Alexandrium minutum cultures was compared using two new methods based on Magnetisable Solid Phase Support (MSPS) techniques with that using three commercial kits. Genomic DNA recovery and PCR amplification were observed and the results obtained from culture samples were validated using field samples. Among the DNA extraction techniques considered, the MSPS methods provided the best results.
引用
收藏
页码:223 / 229
页数:7
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