<HashMap><database>GEO</database><file_versions><headers><Content-Type>application/xml</Content-Type></headers><body><files><Other>ftp://ftp.ncbi.nlm.nih.gov/geo/series/GSE96nnn/GSE96551/</Other></files><type>primary</type></body><statusCode>OK</statusCode><statusCodeValue>200</statusCodeValue></file_versions><scores/><additional><omics_type>Transcriptomics</omics_type><species>Escherichia coli</species><gds_type>Expression profiling by high throughput sequencing</gds_type><full_dataset_link>https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE96551</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>Genome-wide analysis of the differentially expressed genes between a butanol-producing wild type strain and a pykA mutant during fermentation</name><description>To analyze the change of transcription pattern and differentially expressed genes caused by pykA inactivation as the pykA mutant showed a longer growth cycle, increased butanol titer and less pyruvate accumulation. Some new target genes may be used for further metabolic engineering.</description><dates><publication>2017/04/07</publication></dates><accession>GSE96551</accession><cross_references><GSM>GSM2535435</GSM><GSM>GSM2535436</GSM><GSM>GSM2535437</GSM><GSM>GSM2535438</GSM><GSM>GSM2535439</GSM><GSM>GSM2535440</GSM><GSM>GSM2535430</GSM><GSM>GSM2535441</GSM><GSM>GSM2535431</GSM><GSM>GSM2535442</GSM><GSM>GSM2535432</GSM><GSM>GSM2535443</GSM><GSM>GSM2535433</GSM><GSM>GSM2535444</GSM><GSM>GSM2535434</GSM><GSM>GSM2535445</GSM><GPL>14548</GPL><SRA>SRP101799</SRA><GSE>96551</GSE><taxon>Escherichia coli</taxon><PMID>[28363967]</PMID></cross_references></HashMap>