Pan Y, Bodrossy L, Frenzel P, Hestnes AG, Krause S, Luke C,

Pan Y, Bodrossy L, Frenzel P, Hestnes AG, Krause S, Luke C, BTK inhibitor Meima-Franke M, Siljanen H, Svenning MM, Bodelier PL: Impacts of Inter- and Intralaboratory Variations on the Reproducibility of Microbial Community

Analyses. Appl Environ Microbiol 2010, 76:7451-7458.PubMedCrossRef 47. Angiuoli SV, Matalka M, Gussman A, Galens K, Vangala M, Riley DR, Arze C, White JR, White O, Fricke WF: CloVR: a virtual machine for automated and portable sequence analysis from the desktop using cloud computing. BMC Bioinforma 2011, 12:356.CrossRef 48. Caporaso JG, Kuczynski J, Stombaugh J, Bittinger K, Bushman FD, Costello EK, Fierer N, Pena AG, Goodrich JK, Gordon JI: QIIME allows analysis of high-throughput community sequencing data. Nat Methods 2010, 7:335-336.PubMedCrossRef 49. Schloss PD, Westcott SL, Ryabin T, Hall JR, Hartmann M, Hollister EB, Lesniewski RA, Oakley BB, Parks DH, Robinson CJ: Introducing mothur: open-source, platform-independent, community-supported software for describing and comparing microbial communities. Appl Environ Microbiol 2009, 75:7537-7541.PubMedCrossRef 50. Edgar RC, Haas BJ, Clemente JC, Quince C, Knight R: UCHIME improves sensitivity and speed of chimera detection.

Bioinformatics 2011, 27:2194-2200.PubMedCrossRef 51. Wang Q, Garrity GM, Tiedje JM, Cole JR: Naive Bayesian classifier for rapid assignment of rRNA sequences into the new bacterial taxonomy. Appl Environ Microbiol 2007, 73:5261-5267.PubMedCrossRef 52. White JR, Arze C, Team TC, Matalka M, White O: CloVR-16S: Phylogenetic microbial community composition analysis based on 16S ribosomal RNA amplicon sequencing – standard operating procedure, version 1.1. http://​precedings.​nature.​com/​documents/​5888/​version/​2 Temsirolimus cell line Authors’ contributions JK, AO, and TL conceived the study and participated in its design. AO and TL performed all lab work. JW performed data analysis. TL drafted the manuscript. AO, JW, JK, MA, and EB contributed to the draft of the manuscript. All authors read and approved the final manuscript.”
“Background Streptomyces species are widely distributed in natural habitats, such

as soils, lakes, plants and some extreme environments [1, 2]. They are Gram-positive, mycelial bacteria with high G+C content (often >70%) in their DNA [3]. More selleck products than 6000 antibiotics and pharmacologically active metabolites (e.g. antiparasitic and antitumor agents, immuno-suppressants etc.) have been discovered in Streptomyces species [4]. Streptomyces species usually harbor conjugative plasmids [5]. Modes of plasmid replication in Streptomyces include rolling-circle (RC) (e.g. pIJ101, pJV1, pSG5, pSN22, pSVH1, pSB24.2, pSY10 and pSNA1) [6], and uni-directional or bi-directional theta types (e.g. SCP2, pFP11 and pFP1) [7, 8]. Some plasmids (e.g. SLP1 and pSAM2) replicate in chromosomally-integrating/autonomous forms [9–11]. Streptomyces RC plasmids are usually small (8–13 kb), while theta-type plasmids are larger (31–120 kb).

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