<HashMap><database>NODE</database><scores/><additional><omics_type>Genomics</omics_type><submitter>Biao Tang</submitter><experiment_platform>454 GS FLX Titanium</experiment_platform><full_dataset_link>https://www.biosino.org/node/experiment/detail/OEX00000098</full_dataset_link><experiment_library_selection>PCR</experiment_library_selection><sample_count>1</sample_count><experiment_protocol>This genome was sequenced by Roche 454 GS FLX Titanium system and reads were assembled using the Newbler Program (version 2.7). The relationship among contigs was displayed using ContigScape and confirmed by PCR. Sanger-based sequencing was employed to facilitate gap closing and to amend the low-quality regions. The final sequence assembly was conducted using the Phred/Phrap/Consed package.</experiment_protocol><taxonomy>['Burkholderiales']</taxonomy><repository>NODE</repository></additional><is_claimable>false</is_claimable><name>NODEX_Biao_1710141907</name><description>[Polyangium] brachysporum DSM7029 can produce glidobactin, which is a peptide-based proteasome inhibitor that shows great potential as an anticancer drug. It  was also found as a heterologous host can produce another useful NRPS−PKS hybrid molecules epothilones. To better understand the glidobactin biosynthesis mechanism and to aid further studies of this strain, we sequenced this genome.</description><dates><publication>2019-05-31</publication><submission>2017-10-14</submission></dates><accession>OEX00000098</accession><cross_references><NODE>OEP00000097</NODE></cross_references></HashMap>