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identifier DRS107613
type sra-sample
sameAs
organism Paulinella micropora
attributes
strain  MYN1
collection_date  2009-10-09
isol_growth_condt  10.1111/jeu.12102
env_feature  pond
biotic_relationship  free living
description  P. micropora MYN1 strain was cultured under 14 hours light /10 hours dark photoperiodic cycle at 25 degrees C in the modified Waris-H+Si medium. Light intensity was set at 30-40 microE m-2s-1.
samp_mat_process  For total genomic DNA extraction, P. micropora cells were homogenized using a 30 micrometer clearance glass homogenizer (RD440911, Teraoka co., Ltd, Osaka, Japan) with homogenization buffer (20 mM Tris-HCl (pH7.6), 10 mM NaCl, 10 mM KCl, 2.5 mM EDTA, 250 mM sucrose, 0.1 mM spermine, 0.5 mM spermidine, 1 mM DTT). The homogenates were centrifuged at 1000 x g for 10 minutes at 4 degrees C, and the pellets were incubated in lysis buffer (10 mM Tris-HCl (pH 8.0), 1 mM EDTA, 1% SDS, 100 microgram/ml proteinase K) at 55 degrees C for 2 hours, followed by phenol/chloroform extraction and alcohol precipitation to obtain total genomic DNA fraction.
bioproject_id  PRJDB3528
estimated_size  1.35 Gb
project_name  Genome- and transcriptome-analysis of the photosynthetic testate amoeba Paulinella micropora
sample_title  P. micropora total genome
samp_collect_device  P. micropora cells were harvested by low-speed centrifugation (500 x g, 2 minutes) at 4 degrees C. The harvested cells were passed through miracloth (Merk Millipore, Darmstadt, Germany) and 20 micrometer mesh-filter (HD-20, Nippon Rikagaku kikai co. Ltd, Tokyo, Japan) to eliminate contaminating bacteria that were enriched in the dead P. micropora cell aggregates larger than 20 micrometer, and followed by the washing with 10 mM Tris-HCl (pH8.0) three times, and with 10 mM Tris-HCl (pH8.0) plus 10 mM EDTA six times. Next, to remove the cell debris smaller than 5 micrometer, the cells were trapped on 5 micrometer mesh-filter (PP-5n, Kyoshin Rikoh Inc, Tokyo, Japan) and washed with 5 ml TE buffer. The recovered cells were kept at -80 degrees C.
ploidy  missing
propagation  eukaryote: asexual
env_material  missing
num_replicons  missing
geo_loc_name  Japan:Ibaraki, Tsukuba
trophic_level  photoautotroph
env_biome  fresh water
lat_lon  36.0485 N 140.1190 E
biomaterial_provider  Mami Nomura, Ken-ichiro Ishida, Graduate School of Life and Environmental Science, University of Tsukuba
sample_name  P. micropora total genome
properties 
{...}
dbXrefs
bioproject  PRJDB3528
sra-run  DRR030774DRR030775DRR030776DRR030777
sra-submission  DRA003106
biosample  SAMD00026529
sra-study  DRP005442
sra-experiment  DRX027784DRX027785DRX027786DRX027787
distribution JSONJSON-LD
Download
DRA003106.sample.xml  HTTPS FTP
status public
visibility unrestricted-access
dateCreated 2015-03-06T02:08:56+09:00
dateModified 2019-09-15T23:26:39+09:00
datePublished 2019-09-15T23:26:39+09:00