<?xml version="1.0" encoding="UTF-8"?>
<SAMPLE_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <SAMPLE alias="Complete mitochondrial Physarum polycephalum RNA" center_name="The Ohio State University" accession="SRS152873">
    <IDENTIFIERS>
      <PRIMARY_ID>SRS152873</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioSample">SAMN00191251</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>Complete characterization of the edited transcriptome of the mitochondrion of Physarum polycephalum using deep sequencing of RNA</TITLE>
    <SAMPLE_NAME>
      <TAXON_ID>5791</TAXON_ID>
      <SCIENTIFIC_NAME>Physarum polycephalum</SCIENTIFIC_NAME>
    </SAMPLE_NAME>
    <DESCRIPTION>Plasmodial strain M3CVIII (kindly provided by Dr. Mark Adelman) was grown as macroplasmodia at 26*C in semi-defined medium.  Macroplasmodia were harvested directly into ice cold BSS [10 mM Tris-HCl (pH 7.5)/ 0.25 M sucrose], with all subsequent steps carried out at 4*C.  Cells were lysed in a Waring blender using two 15 second bursts at half maximum speed.  The homogenate was filtered prior to pelleting the nuclei and remaining cell debris by centrifugation for 5 min at 700xg.  Mitochondria were pelleted by centrifugation for 5 min at 5800xg, resuspended in BSS, layered over Percoll step gradients (densities 1.044-1.095 g/ml in 1 mM Tris-HCl (pH 7.5)/ 0.25 M sucrose), and centrifuged at 47,800xg for 30 seconds.  Mitochondrial fractions were collected from each gradient, diluted slowly with 2.5 volumes of 1 mM Tris-HCl (pH 7.5)/ 0.25 M sucrose, and pelleted by centrifugation at 7,600g for 5 min.  Total mitochondrial RNA was isolated using TRIzol reagent (Invitrogen) as specified by the manufacturer.  Residual DNA was removed by digestion with DNaseI (Roche) in the supplied buffer.</DESCRIPTION>
  </SAMPLE>
</SAMPLE_SET>
