A simplified rapid, low-cost and versatile DNA-based assessment of soil microbial biomass

被引:81
作者
Fornasier, F. [1 ]
Ascher, J. [2 ,3 ]
Ceccherini, M. T. [3 ]
Tomat, E. [1 ]
Pietramellara, G. [3 ]
机构
[1] Ctr Ric Studio Relaz Tra Pianta & Suolo, Consiglio Ric & Sperimentaz Agr, I-34170 Gorizia, Italy
[2] Univ Innsbruck, Inst Microbiol, A-6020 Innsbruck, Austria
[3] Univ Florence, Dept Agrifood & Environm Sci, I-50144 Florence, Italy
关键词
Soil microbial biomass; Double stranded DNA (dsDNA); Bio-indicator; EXTRACTION METHOD; ORGANIC-MATTER; PURIFICATION; COMMUNITIES; BACTERIAL; DSDNA; QUANTIFICATION; TRANSFORMATION; MICROFLORA; INDEXES;
D O I
10.1016/j.ecolind.2014.03.028
中图分类号
X176 [生物多样性保护];
学科分类号
090705 ;
摘要
We set up a simple, culture independent, low-cost and high-throughput method for DNA-based quantitative assessment of soil microbial biomass using eight soils covering a wide range of physico-chemical properties. DNA was extracted with a 0.12 M, pH 8 Na2HPO4 buffer using bead beating; double stranded DNA (dsDNA) was quantified in a crude (not purified) extract using PicoGreen reagent. In contrast to yields obtained by using a commercial standard method (FastDNA Kit for soil, MP-Biomedicals), our yields of dsDNA were generally higher, most probably because any purification method for obtaining highly pure DNA for downstream analyses leads to DNA loss. These results suggest the new method provides more reliable quantitative data; thus it is a good environmental indicator, as an underestimation of the soil microbial biomass due to DNA loss during purification can be excluded. The ratio between microbial C (Cmic) obtained by the traditional, widely used fumigation-extraction method and dsDNA ranged from 12.0 to 63.5 mu g Cmic per mu g dsDNA. Crude DNA obtained by the new method as well as purified DNA obtained by using the commercial kit were compared in terms of quantity (fluorometry; spectrophotometry) and quality (purity indices: A(260)/A(280),A(260)/A(230); PCR compatibility; gel electrophoresis: molecular weight and molecular integrity). Our results suggest that the new method provides a high-throughput estimator of microbial biomass (expressed as mu gdsDNAg(-1) soil) in soils having widely different properties without the need for high-cost commercial extraction kits and/or cumbersome individual methods. Due to its simplicity, speed and low-cost, our method is capable for routine quantitative assessments of soil microbial biomass, assessable also for soil scientists with laboratories that are otherwise not equipped for molecular analyses. (C) 2014 Elsevier Ltd. All rights reserved.
引用
收藏
页码:75 / 82
页数:8
相关论文
共 49 条
[1]   Distribution of microbial communities in a forest soil profile investigated by microbial biomass, soil respiration and DGGE of total and extracellular DNA [J].
Agnelli, A ;
Ascher, J ;
Corti, G ;
Ceccherini, MT ;
Nannipieri, P ;
Pietramellara, G .
SOIL BIOLOGY & BIOCHEMISTRY, 2004, 36 (05) :859-868
[2]   Purification and isotopic signatures (δ13C, δ 15N, Δ14C) of soil extracellular DNA [J].
Agnelli, Alberto ;
Ascher, Judith ;
Corti, Giuseppe ;
Ceccherini, Maria Teresa ;
Pietramellara, Giacomo ;
Nannipieri, Paolo .
BIOLOGY AND FERTILITY OF SOILS, 2007, 44 (02) :353-361
[3]   PHYSIOLOGICAL METHOD FOR QUANTITATIVE MEASUREMENT OF MICROBIAL BIOMASS IN SOILS [J].
ANDERSON, JPE ;
DOMSCH, KH .
SOIL BIOLOGY & BIOCHEMISTRY, 1978, 10 (03) :215-221
[4]   Are humus forms, mesofauna and microflora in subalpine forest soils sensitive to thermal conditions? [J].
Ascher, J. ;
Sartori, G. ;
Graefe, U. ;
Thornton, B. ;
Ceccherini, M. T. ;
Pietramellara, G. ;
Egli, M. .
BIOLOGY AND FERTILITY OF SOILS, 2012, 48 (06) :709-725
[5]   Evaluation of the denaturing gradient gel electrophoresis-apparatus as a parameter influencing soil microbial community fingerprinting [J].
Ascher, J. ;
Ceccherini, M. T. ;
Chronakova, A. ;
Jirout, J. ;
Borgogni, F. ;
Elhottova, D. ;
Simek, M. ;
Pietramellara, G. .
WORLD JOURNAL OF MICROBIOLOGY & BIOTECHNOLOGY, 2010, 26 (09) :1721-1726
[6]   Sequential extraction and genetic fingerprinting of a forest soil metagenome [J].
Ascher, J. ;
Ceccherini, M. T. ;
Pantani, O. L. ;
Agnelli, A. ;
Borgogni, F. ;
Guerri, G. ;
Nannipieri, P. ;
Pietramellara, G. .
APPLIED SOIL ECOLOGY, 2009, 42 (02) :176-181
[7]   Composition, biomass and activity of microflora, and leaf yields and foliar elemental concentrations of lettuce, after in situ stabilization of an arsenic-contaminated soil [J].
Ascher, J. ;
Ceccherini, M. T. ;
Landi, L. ;
Mench, M. ;
Pietramellara, G. ;
Nannipieri, P. ;
Renella, G. .
APPLIED SOIL ECOLOGY, 2009, 41 (03) :351-359
[8]   Molecular breeding of polymerases for resistance to environmental inhibitors [J].
Baar, Claudia ;
d'Abbadie, Marc ;
Vaisman, Alexandra ;
Arana, Mercedes E. ;
Hofreiter, Michael ;
Woodgate, Roger ;
Kunkel, Thomas A. ;
Holliger, Philipp .
NUCLEIC ACIDS RESEARCH, 2011, 39 (08) :e51
[9]   Effects of humic substances on fluorometric DNA quantification and DNA hybridization [J].
Bachoon, DS ;
Otero, E ;
Hodson, RE .
JOURNAL OF MICROBIOLOGICAL METHODS, 2001, 47 (01) :73-82
[10]   Turnover of soil organic matter and of microbial biomass under C3-C4 vegetation change: Consideration of 13C fractionation and preferential substrate utilization [J].
Blagodatskaya, E. ;
Yuyukina, T. ;
Blagodatsky, S. ;
Kuzyakov, Y. .
SOIL BIOLOGY & BIOCHEMISTRY, 2011, 43 (01) :159-166