Novel oligonucleotide primers reveal a high diversity of microbes which drive phosphorous turnover in soil

被引:83
作者
Bergkemper, Fabian [1 ]
Kublik, Susanne [1 ]
Lang, Friederike [2 ]
Krueger, Jaane [2 ]
Vestergaard, Gisle [1 ]
Schloter, Michael [1 ]
Schulz, Stefanie [1 ]
机构
[1] Helmholtz Zentrum Munchen, Res Unit Environm Genom, Ingolstadter Landstr 1, D-85764 Neuherberg, Germany
[2] Univ Freiburg, Bodenokol, Bertoldstr 17, D-79085 Freiburg, Germany
关键词
Phosphorus turnover; Forest soil; phoD; phoN; appA; pitA; pstS; ALKALINE-PHOSPHATASE; GENE; PHYTASE; IDENTIFICATION; COMMUNITY; PRODUCT; CLONING;
D O I
10.1016/j.mimet.2016.04.011
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Phosphorus (P) is of central importance for cellular life but likewise a limiting macronutrient in numerous environments. Certainly microorganisms have proven their ability to increase the phosphorus bioavailability by mineralization of organic-P and solubilization of inorganic-P. On the other hand they efficiently take up P and compete with other biota for phosphorus. However the actual microbial community that is associated to the turnover of this crucial macronutrient in different ecosystems remains largely anonymous especially taking effects of seasonality and spatial heterogeneity into account. In this study seven oligonucleotide primers are presented which target genes coding for microbial acid and alkaline phosphatases (phoN, phoD), phytases (appA), phosphonatases (phnX) as well as the quinoprotein glucose dehydrogenase (gcd) and different P transporters (pitA, pstS). Illumina amplicon sequencing of soil genomic DNA underlined the high rate of primer specificity towards the respective target gene which usually ranged between 98% and 100% (phoN: 87%). As expected the primers amplified genes from a broad diversity of distinct microorganisms. Using DNA from a beech dominated forest soil, the highest microbial diversity was detected for the alkaline phosphatase (phoD) gene which was amplified from 15 distinct phyla respectively 81 families. Noteworthy the primers also allowed amplification of phoD from 6 fungal orders. The genes coding for acid phosphatase (phoN) and the quinoprotein glucose dehydrogenase (gcd) were amplified from 20 respectively 17 different microbial orders. In comparison the phytase and phosphonatase (appA, phnX) primers covered 13 bacterial orders from 2 different phyla respectively. Although the amplified microbial diversity was apparently limited both primers reliably detected all orders that contributed to the P turnover in the investigated soil as revealed by a previous metagenomic approach. Genes that code for microbial P transporter (pitA, pstS) were amplified from 13 respectively 9 distinct microbial orders. Accordingly the introduced primers represent a valuable tool for further analysis of the microbial community involved in the turnover of phosphorus in soils but most likely also in other environments. (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:91 / 97
页数:7
相关论文
共 39 条
[1]  
[Anonymous], R LANG ENV STAT COMP
[2]  
[Anonymous], ENV MICROBIOL
[3]   Active and total microbial communities in forest soil are largely different and highly stratified during decomposition [J].
Baldrian, Petr ;
Kolarik, Miroslav ;
Stursova, Martina ;
Kopecky, Jan ;
Valaskova, Vendula ;
Vetrovsky, Tomaas ;
Zifcakova, Lucia ;
Snajdr, Jaroslav ;
Ridl, Jakub ;
Vlcek, Cestmir ;
Voriskova, Jana .
ISME JOURNAL, 2012, 6 (02) :248-258
[4]   Fast and sensitive protein alignment using DIAMOND [J].
Buchfink, Benjamin ;
Xie, Chao ;
Huson, Daniel H. .
NATURE METHODS, 2015, 12 (01) :59-60
[5]   QIIME allows analysis of high-throughput community sequencing data [J].
Caporaso, J. Gregory ;
Kuczynski, Justin ;
Stombaugh, Jesse ;
Bittinger, Kyle ;
Bushman, Frederic D. ;
Costello, Elizabeth K. ;
Fierer, Noah ;
Pena, Antonio Gonzalez ;
Goodrich, Julia K. ;
Gordon, Jeffrey I. ;
Huttley, Gavin A. ;
Kelley, Scott T. ;
Knights, Dan ;
Koenig, Jeremy E. ;
Ley, Ruth E. ;
Lozupone, Catherine A. ;
McDonald, Daniel ;
Muegge, Brian D. ;
Pirrung, Meg ;
Reeder, Jens ;
Sevinsky, Joel R. ;
Tumbaugh, Peter J. ;
Walters, William A. ;
Widmann, Jeremy ;
Yatsunenko, Tanya ;
Zaneveld, Jesse ;
Knight, Rob .
NATURE METHODS, 2010, 7 (05) :335-336
[6]   CLONING, MAPPING, AND SEQUENCING OF THE GENE ENCODING ESCHERICHIA-COLI QUINOPROTEIN GLUCOSE-DEHYDROGENASE [J].
CLETONJANSEN, AM ;
GOOSEN, N ;
FAYET, O ;
VANDEPUTTE, P .
JOURNAL OF BACTERIOLOGY, 1990, 172 (11) :6308-6315
[7]   Accessing the Soil Metagenome for Studies of Microbial Diversity [J].
Delmont, Tom O. ;
Robe, Patrick ;
Cecillon, Sebastien ;
Clark, Ian M. ;
Constancias, Florentin ;
Simonet, Pascal ;
Hirsch, Penny R. ;
Vogel, Timothy M. .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 2011, 77 (04) :1315-1324
[8]   A Bacillus subtilis secreted phosphodiesterase alkaline phosphatase is the product of a Pho regulon gene, phoD [J].
Eder, S ;
Shi, L ;
Jensen, K ;
Yamane, K ;
Hulett, FM .
MICROBIOLOGY-SGM, 1996, 142 :2041-2047
[9]   Phosphorus: a limiting nutrient for humanity? [J].
Elser, James J. .
CURRENT OPINION IN BIOTECHNOLOGY, 2012, 23 (06) :833-838
[10]   MOLECULAR-CLONING OF THE PHOSPHATE (INORGANIC) TRANSPORT (PIT) GENE OF ESCHERICHIA-COLI-K12 - IDENTIFICATION OF THE PIT+ GENE-PRODUCT AND PHYSICAL MAPPING OF THE PIT-GOR REGION OF THE CHROMOSOME [J].
ELVIN, CM ;
DIXON, NE ;
ROSENBERG, H .
MOLECULAR & GENERAL GENETICS, 1986, 204 (03) :477-484