Electroelution to remove humic compounds from soil DNA and RNA extracts

被引:28
作者
Chandler, DP
Schreckhise, RW
Smith, JL
Bolton, H
机构
[1] FRED HUTCHINSON CANC RES CTR, SEATTLE, WA 98104 USA
[2] WASHINGTON STATE UNIV, USDA ARS, PULLMAN, WA 99161 USA
关键词
electroelution; humics; PCR; rRNA; soil; 16S;
D O I
10.1016/S0167-7012(96)00957-8
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The application of nucleic acid techniques to detect, identify, and monitor specific genes or organisms in soils or sediments is often complicated by the inhibitory effects of humic compounds that copurify with nucleic acids. A rapid electroelution technique was developed to separate inhibitory compounds from extracts of soil DNA and RNA. This technique was used in conjunction with PCR to detect nifH, terrestrial ammonia-oxidizer (TAO) 16S rRNA genes and TAO 16S rRNA from a variety of surface soils and contaminated sediments. After electroelution of crude nucleic acid extracts, PCR sensitivity was increased up to a factor of 10(4) relative to DNA templates that had not been electroeluted. Without electroelution of crude DNA extracts, target genes often remained undetected. Likewise, electroelution of crude RNA extracts increased RT-PCR sensitivity (for TAO 16S rRNA) by a factor of 10(3) relative to RNA extracts that had not been further purified. The electroelution technique will therefore be useful for rendering environmental nucleic acids extracted from soil and sediment more amenable to PCR methods and nucleic acid analysis.
引用
收藏
页码:11 / 19
页数:9
相关论文
共 23 条
[1]   SOIL MICROBIAL BIOMASS AND ACTIVITY OF A DISTURBED AND UNDISTURBED SHRUB-STEPPE ECOSYSTEM [J].
BOLTON, H ;
SMITH, JL ;
LINK, SO .
SOIL BIOLOGY & BIOCHEMISTRY, 1993, 25 (05) :545-552
[2]   NITROGEN MINERALIZATION POTENTIALS OF SHRUB-STEPPE SOILS WITH DIFFERENT DISTURBANCE HISTORIES [J].
BOLTON, H ;
SMITH, JL ;
WILDUNG, RE .
SOIL SCIENCE SOCIETY OF AMERICA JOURNAL, 1990, 54 (03) :887-891
[3]  
Bremner J.M., 1982, AGRONOMY, P595, DOI DOI 10.2134/AGR0NM0N0GR9.2.2ED.C31
[4]   Estimating biodegradative gene numbers at a JP-5 contaminated site using PCR [J].
Chandler, DP ;
Brockman, FJ .
APPLIED BIOCHEMISTRY AND BIOTECHNOLOGY, 1996, 57-8 :971-982
[5]   POLYMERASE CHAIN-REACTION AMPLIFICATION OF NAPHTHALENE-CATABOLIC AND 16S RIBOSOMAL-RNA GENE-SEQUENCES FROM INDIGENOUS SEDIMENT BACTERIA [J].
HERRICK, JB ;
MADSEN, EL ;
BATT, CA ;
GHIORSE, WC .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 1993, 59 (03) :687-694
[7]   DEVELOPMENT AND APPLICATION OF A NEW METHOD TO EXTRACT BACTERIAL-DNA FROM SOIL BASED ON SEPARATION OF BACTERIA FROM SOIL WITH CATION-EXCHANGE RESIN [J].
JACOBSEN, CS ;
RASMUSSEN, OF .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 1992, 58 (08) :2458-2462
[8]   Estimation of the abundance of an uncultured soil bacterial strain by a competitive quantitative PCR method [J].
Lee, SY ;
Bollinger, J ;
Bezdicek, D ;
Ogram, A .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 1996, 62 (10) :3787-3793
[9]  
Nelson D. W., 1982, Methods of soil analysis. Part 2. Chemical and microbiological properties, P539
[10]   ISOLATION AND CHARACTERIZATION OF RNA FROM LOW-BIOMASS DEEP-SUBSURFACE SEDIMENTS [J].
OGRAM, A ;
SUN, WH ;
BROCKMAN, FJ ;
FREDRICKSON, JK .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 1995, 61 (02) :763-768