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    <TITLE>GSM4194469: A1 strain AWRI R2 was cultivated  with 0 g/L PAs; Saccharomyces cerevisiae; RNA-Seq</TITLE>
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        <LIBRARY_CONSTRUCTION_PROTOCOL>Yeast cells were grinded in liquid nitrogen. Total RNA of each sample was extracted using RNeasy Mini Kit (Qiagen). One microgram of total RNA passing the quality test was used for library preparation based on the manufacturer's protocol (NEBNext® Ultra™ RNA Library Prep Kit for Illumina®). After quantity and quality evaluation, Illumina HiSeq sequencing platform was employed for the library sequencing at GENEWIZ (Suzhou, China).</LIBRARY_CONSTRUCTION_PROTOCOL>
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      <PRIMARY_ID>SRX7223645</PRIMARY_ID>
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    <TITLE>GSM4194470: A2 strain AWRI R2 was cultivated  with 0 g/L PAs; Saccharomyces cerevisiae; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP233369" refname="GSE141069">
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        <PRIMARY_ID>SRP233369</PRIMARY_ID>
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        <LIBRARY_CONSTRUCTION_PROTOCOL>Yeast cells were grinded in liquid nitrogen. Total RNA of each sample was extracted using RNeasy Mini Kit (Qiagen). One microgram of total RNA passing the quality test was used for library preparation based on the manufacturer's protocol (NEBNext® Ultra™ RNA Library Prep Kit for Illumina®). After quantity and quality evaluation, Illumina HiSeq sequencing platform was employed for the library sequencing at GENEWIZ (Suzhou, China).</LIBRARY_CONSTRUCTION_PROTOCOL>
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      <PRIMARY_ID>SRX7223646</PRIMARY_ID>
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    <TITLE>GSM4194471: A3 strain AWRI R2 was cultivated  with 0 g/L PAs; Saccharomyces cerevisiae; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP233369" refname="GSE141069">
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        <PRIMARY_ID>SRP233369</PRIMARY_ID>
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          <PRIMARY_ID>SRS5724831</PRIMARY_ID>
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        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
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          <PAIRED/>
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        <LIBRARY_CONSTRUCTION_PROTOCOL>Yeast cells were grinded in liquid nitrogen. Total RNA of each sample was extracted using RNeasy Mini Kit (Qiagen). One microgram of total RNA passing the quality test was used for library preparation based on the manufacturer's protocol (NEBNext® Ultra™ RNA Library Prep Kit for Illumina®). After quantity and quality evaluation, Illumina HiSeq sequencing platform was employed for the library sequencing at GENEWIZ (Suzhou, China).</LIBRARY_CONSTRUCTION_PROTOCOL>
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      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
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      <PRIMARY_ID>SRX7223647</PRIMARY_ID>
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    <TITLE>GSM4194472: B1 strain AWRI R2 was cultivated  with 0.1 g/L Pas; Saccharomyces cerevisiae; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP233369" refname="GSE141069">
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        <PRIMARY_ID>SRP233369</PRIMARY_ID>
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      <SAMPLE_DESCRIPTOR accession="SRS5724832">
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          <PRIMARY_ID>SRS5724832</PRIMARY_ID>
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        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
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          <PAIRED/>
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        <LIBRARY_CONSTRUCTION_PROTOCOL>Yeast cells were grinded in liquid nitrogen. Total RNA of each sample was extracted using RNeasy Mini Kit (Qiagen). One microgram of total RNA passing the quality test was used for library preparation based on the manufacturer's protocol (NEBNext® Ultra™ RNA Library Prep Kit for Illumina®). After quantity and quality evaluation, Illumina HiSeq sequencing platform was employed for the library sequencing at GENEWIZ (Suzhou, China).</LIBRARY_CONSTRUCTION_PROTOCOL>
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        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
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      <PRIMARY_ID>SRX7223648</PRIMARY_ID>
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    <TITLE>GSM4194473: B2 strain AWRI R2 was cultivated  with 0.1 g/L Pas; Saccharomyces cerevisiae; RNA-Seq</TITLE>
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        <PRIMARY_ID>SRP233369</PRIMARY_ID>
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        <LIBRARY_CONSTRUCTION_PROTOCOL>Yeast cells were grinded in liquid nitrogen. Total RNA of each sample was extracted using RNeasy Mini Kit (Qiagen). One microgram of total RNA passing the quality test was used for library preparation based on the manufacturer's protocol (NEBNext® Ultra™ RNA Library Prep Kit for Illumina®). After quantity and quality evaluation, Illumina HiSeq sequencing platform was employed for the library sequencing at GENEWIZ (Suzhou, China).</LIBRARY_CONSTRUCTION_PROTOCOL>
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        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
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      <PRIMARY_ID>SRX7223649</PRIMARY_ID>
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    <TITLE>GSM4194474: B3 strain AWRI R2 was cultivated  with 0.1 g/L Pas; Saccharomyces cerevisiae; RNA-Seq</TITLE>
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        <PRIMARY_ID>SRP233369</PRIMARY_ID>
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          <PRIMARY_ID>SRS5724834</PRIMARY_ID>
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        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
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          <PAIRED/>
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        <LIBRARY_CONSTRUCTION_PROTOCOL>Yeast cells were grinded in liquid nitrogen. Total RNA of each sample was extracted using RNeasy Mini Kit (Qiagen). One microgram of total RNA passing the quality test was used for library preparation based on the manufacturer's protocol (NEBNext® Ultra™ RNA Library Prep Kit for Illumina®). After quantity and quality evaluation, Illumina HiSeq sequencing platform was employed for the library sequencing at GENEWIZ (Suzhou, China).</LIBRARY_CONSTRUCTION_PROTOCOL>
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        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
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      <PRIMARY_ID>SRX7223650</PRIMARY_ID>
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    <TITLE>GSM4194475: C1 strain AWRI R2 was cultivated  with 1.0 g/L PAs; Saccharomyces cerevisiae; RNA-Seq</TITLE>
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        <LIBRARY_CONSTRUCTION_PROTOCOL>Yeast cells were grinded in liquid nitrogen. Total RNA of each sample was extracted using RNeasy Mini Kit (Qiagen). One microgram of total RNA passing the quality test was used for library preparation based on the manufacturer's protocol (NEBNext® Ultra™ RNA Library Prep Kit for Illumina®). After quantity and quality evaluation, Illumina HiSeq sequencing platform was employed for the library sequencing at GENEWIZ (Suzhou, China).</LIBRARY_CONSTRUCTION_PROTOCOL>
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        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
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      <PRIMARY_ID>SRX7223651</PRIMARY_ID>
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    <TITLE>GSM4194476: C2 strain AWRI R2 was cultivated  with 1.0 g/L PAs; Saccharomyces cerevisiae; RNA-Seq</TITLE>
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        <PRIMARY_ID>SRP233369</PRIMARY_ID>
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          <PRIMARY_ID>SRS5724836</PRIMARY_ID>
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          <PAIRED/>
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        <LIBRARY_CONSTRUCTION_PROTOCOL>Yeast cells were grinded in liquid nitrogen. Total RNA of each sample was extracted using RNeasy Mini Kit (Qiagen). One microgram of total RNA passing the quality test was used for library preparation based on the manufacturer's protocol (NEBNext® Ultra™ RNA Library Prep Kit for Illumina®). After quantity and quality evaluation, Illumina HiSeq sequencing platform was employed for the library sequencing at GENEWIZ (Suzhou, China).</LIBRARY_CONSTRUCTION_PROTOCOL>
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        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
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    <TITLE>GSM4194477: C3 strain AWRI R2 was cultivated  with 1.0 g/L PAs; Saccharomyces cerevisiae; RNA-Seq</TITLE>
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        <PRIMARY_ID>SRP233369</PRIMARY_ID>
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      <DESIGN_DESCRIPTION/>
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          <PRIMARY_ID>SRS5724837</PRIMARY_ID>
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        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
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          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Yeast cells were grinded in liquid nitrogen. Total RNA of each sample was extracted using RNeasy Mini Kit (Qiagen). One microgram of total RNA passing the quality test was used for library preparation based on the manufacturer's protocol (NEBNext® Ultra™ RNA Library Prep Kit for Illumina®). After quantity and quality evaluation, Illumina HiSeq sequencing platform was employed for the library sequencing at GENEWIZ (Suzhou, China).</LIBRARY_CONSTRUCTION_PROTOCOL>
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    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
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