Comparative genome‐scale analysis of Pichia pastoris variants informs selection of an optimal base strain
Komagataella phaffii, also known as Pichia pastoris, is a common host for the production of biologics and enzymes, due to fast growth, high productivity, and advancements in host engineering. Several K. phaffii variants are commonly used as interchangeable base strains, which confounds efforts to im...
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description | Komagataella phaffii, also known as Pichia pastoris, is a common host for the production of biologics and enzymes, due to fast growth, high productivity, and advancements in host engineering. Several K. phaffii variants are commonly used as interchangeable base strains, which confounds efforts to improve this host. In this study, genomic and transcriptomic analyses of Y‐11430 (CBS7435), GS115, X‐33, and eight other variants enabled a comparative assessment of the relative fitness of these hosts for recombinant protein expression. Cell wall integrity explained the majority of the variation among strains, impacting transformation efficiency, growth, methanol metabolism, and secretion of heterologous proteins. Y‐11430 exhibited the highest activity of genes involved in methanol utilization, up to two‐fold higher transcription of heterologous genes, and robust growth. With a more permeable cell wall, X‐33 displayed a six‐fold higher transformation efficiency and up to 1.2‐fold higher titers than Y‐11430. X‐33 also shared nearly all mutations, and a defective variant of HIS4, with GS115, precluding robust growth. Transferring two beneficial mutations identified in X‐33 into Y‐11430 resulted in an optimized base strain that provided up to four‐fold higher transformation efficiency and three‐fold higher protein titers, while retaining robust growth. The approach employed here to assess unique banked variants in a species and then transfer key beneficial variants into a base strain should also facilitate rational assessment of a broad set of other recombinant hosts.
Pichia pastoris is a common host for the production of biologics and enzymes, due to fast growth, high productivity, and advancements in host engineering. The authors assessed several P. pastoris variants for relative fitness as recombinant hosts by performing genomic, transcriptomic, and phenotypic analyses on each variant. This genome‐scale approach revealed key beneficial features, which were combined to create a novel, optimized base strain. |
doi_str_mv | 10.1002/bit.27209 |
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Pichia pastoris is a common host for the production of biologics and enzymes, due to fast growth, high productivity, and advancements in host engineering. The authors assessed several P. pastoris variants for relative fitness as recombinant hosts by performing genomic, transcriptomic, and phenotypic analyses on each variant. This genome‐scale approach revealed key beneficial features, which were combined to create a novel, optimized base strain.</description><identifier>ISSN: 0006-3592</identifier><identifier>EISSN: 1097-0290</identifier><identifier>DOI: 10.1002/bit.27209</identifier><identifier>PMID: 31654411</identifier><language>eng</language><publisher>HOBOKEN: Wiley</publisher><subject>Biotechnology & Applied Microbiology ; Cell walls ; Efficiency ; Fungal Proteins - genetics ; Fungal Proteins - metabolism ; Gene Expression Profiling ; Genes ; Genetic transformation ; Genome, Fungal - genetics ; Genomes ; Genomics ; heterologous gene expression ; Life Sciences & Biomedicine ; Metabolism ; Methanol ; Mutation ; Pichia - genetics ; Pichia - metabolism ; Pichia pastoris ; Protein folding ; Proteins ; recombinant protein ; Recombinant Proteins - genetics ; Recombinant Proteins - metabolism ; RNA, Fungal - analysis ; RNA, Fungal - genetics ; RNA‐Seq ; Robustness ; Saccharomycetales - genetics ; Saccharomycetales - metabolism ; Science & Technology ; Sequence Analysis, RNA ; Transcription ; Transcriptome - genetics ; Transformations ; yeast</subject><ispartof>Biotechnology and bioengineering, 2020-02, Vol.117 (2), p.543-555</ispartof><rights>2019 The Authors. published by Wiley Periodicals, Inc.</rights><rights>2019 The Authors. Biotechnology and Bioengineering published by Wiley Periodicals, Inc.</rights><rights>2020 Wiley Periodicals, Inc.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>true</woscitedreferencessubscribed><woscitedreferencescount>31</woscitedreferencescount><woscitedreferencesoriginalsourcerecordid>wos000495855200001</woscitedreferencesoriginalsourcerecordid><citedby>FETCH-LOGICAL-c4809-e190d13a7daca547fbd457133f5a027aaad47360ff5903a285648f17d45d28b83</citedby><cites>FETCH-LOGICAL-c4809-e190d13a7daca547fbd457133f5a027aaad47360ff5903a285648f17d45d28b83</cites><orcidid>0000-0002-2284-3872 ; 0000-0002-2400-0094 ; 0000-0001-7163-9547 ; 0000-0002-7912-0309</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fbit.27209$$EPDF$$P50$$Gwiley$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fbit.27209$$EHTML$$P50$$Gwiley$$Hfree_for_read</linktohtml><link.rule.ids>230,315,781,785,886,1418,27929,27930,28253,45579,45580</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/31654411$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Brady, Joseph R.</creatorcontrib><creatorcontrib>Whittaker, Charles A.</creatorcontrib><creatorcontrib>Tan, Melody C.</creatorcontrib><creatorcontrib>Kristensen, D. Lee</creatorcontrib><creatorcontrib>Ma, Duanduan</creatorcontrib><creatorcontrib>Dalvie, Neil C.</creatorcontrib><creatorcontrib>Love, Kerry Routenberg</creatorcontrib><creatorcontrib>Love, J. Christopher</creatorcontrib><title>Comparative genome‐scale analysis of Pichia pastoris variants informs selection of an optimal base strain</title><title>Biotechnology and bioengineering</title><addtitle>BIOTECHNOL BIOENG</addtitle><addtitle>Biotechnol Bioeng</addtitle><description>Komagataella phaffii, also known as Pichia pastoris, is a common host for the production of biologics and enzymes, due to fast growth, high productivity, and advancements in host engineering. Several K. phaffii variants are commonly used as interchangeable base strains, which confounds efforts to improve this host. In this study, genomic and transcriptomic analyses of Y‐11430 (CBS7435), GS115, X‐33, and eight other variants enabled a comparative assessment of the relative fitness of these hosts for recombinant protein expression. Cell wall integrity explained the majority of the variation among strains, impacting transformation efficiency, growth, methanol metabolism, and secretion of heterologous proteins. Y‐11430 exhibited the highest activity of genes involved in methanol utilization, up to two‐fold higher transcription of heterologous genes, and robust growth. With a more permeable cell wall, X‐33 displayed a six‐fold higher transformation efficiency and up to 1.2‐fold higher titers than Y‐11430. X‐33 also shared nearly all mutations, and a defective variant of HIS4, with GS115, precluding robust growth. Transferring two beneficial mutations identified in X‐33 into Y‐11430 resulted in an optimized base strain that provided up to four‐fold higher transformation efficiency and three‐fold higher protein titers, while retaining robust growth. The approach employed here to assess unique banked variants in a species and then transfer key beneficial variants into a base strain should also facilitate rational assessment of a broad set of other recombinant hosts.
Pichia pastoris is a common host for the production of biologics and enzymes, due to fast growth, high productivity, and advancements in host engineering. The authors assessed several P. pastoris variants for relative fitness as recombinant hosts by performing genomic, transcriptomic, and phenotypic analyses on each variant. This genome‐scale approach revealed key beneficial features, which were combined to create a novel, optimized base strain.</description><subject>Biotechnology & Applied Microbiology</subject><subject>Cell walls</subject><subject>Efficiency</subject><subject>Fungal Proteins - genetics</subject><subject>Fungal Proteins - metabolism</subject><subject>Gene Expression Profiling</subject><subject>Genes</subject><subject>Genetic transformation</subject><subject>Genome, Fungal - genetics</subject><subject>Genomes</subject><subject>Genomics</subject><subject>heterologous gene expression</subject><subject>Life Sciences & Biomedicine</subject><subject>Metabolism</subject><subject>Methanol</subject><subject>Mutation</subject><subject>Pichia - genetics</subject><subject>Pichia - metabolism</subject><subject>Pichia pastoris</subject><subject>Protein folding</subject><subject>Proteins</subject><subject>recombinant protein</subject><subject>Recombinant Proteins - genetics</subject><subject>Recombinant Proteins - metabolism</subject><subject>RNA, Fungal - analysis</subject><subject>RNA, Fungal - genetics</subject><subject>RNA‐Seq</subject><subject>Robustness</subject><subject>Saccharomycetales - genetics</subject><subject>Saccharomycetales - metabolism</subject><subject>Science & Technology</subject><subject>Sequence Analysis, RNA</subject><subject>Transcription</subject><subject>Transcriptome - genetics</subject><subject>Transformations</subject><subject>yeast</subject><issn>0006-3592</issn><issn>1097-0290</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><sourceid>24P</sourceid><sourceid>WIN</sourceid><sourceid>AOWDO</sourceid><sourceid>EIF</sourceid><recordid>eNqNkc1u1DAUhSMEokNhwQugSGyoUFr_xHG8qQQRP5UqwaKsrRvHbl0Se7CdQbPrI_CMPAkOM4wACYmN7Wt_9_jonqJ4itEpRoic9TadEk6QuFesMBK8QkSg-8UKIdRUlAlyVDyK8TaXvG2ah8URxQ2ra4xXxefOT2sIkOxGl9fa-Ul_v_sWFYy6BAfjNtpYelN-tOrGQrmGmHzIVxsIFlyKpXXGhymWUY9aJevdQkNe18lOMJY9RF3GFMC6x8UDA2PUT_b7cfHp7Zur7n11-eHdRffqslJ1i0SlsUADpsAHUMBqbvqhZhxTahggwgFgqDltkDFMIAqkZU3dGswzNZC2b-lxcb7TXc_9pAelXf5-lOuQDYWt9GDlny_O3shrv5EcISooywIv9gLBf5l1THKyUelxBKf9HCWhSNQ8Dxln9Plf6K2fQx7cQtGaiTbrZepkR6ngYwzaHMxgJJcIZY5Q_owws89-d38gf2WWgZc74KvuvYnKaqf0Acsh14K1jJF8Qgvd_j_d2QRLhp2fXcqtZ_tWO-rtvy3L1xdXO-8_AIBayM8</recordid><startdate>202002</startdate><enddate>202002</enddate><creator>Brady, Joseph R.</creator><creator>Whittaker, Charles A.</creator><creator>Tan, Melody C.</creator><creator>Kristensen, D. 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Lee</au><au>Ma, Duanduan</au><au>Dalvie, Neil C.</au><au>Love, Kerry Routenberg</au><au>Love, J. Christopher</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Comparative genome‐scale analysis of Pichia pastoris variants informs selection of an optimal base strain</atitle><jtitle>Biotechnology and bioengineering</jtitle><stitle>BIOTECHNOL BIOENG</stitle><addtitle>Biotechnol Bioeng</addtitle><date>2020-02</date><risdate>2020</risdate><volume>117</volume><issue>2</issue><spage>543</spage><epage>555</epage><pages>543-555</pages><issn>0006-3592</issn><eissn>1097-0290</eissn><abstract>Komagataella phaffii, also known as Pichia pastoris, is a common host for the production of biologics and enzymes, due to fast growth, high productivity, and advancements in host engineering. Several K. phaffii variants are commonly used as interchangeable base strains, which confounds efforts to improve this host. In this study, genomic and transcriptomic analyses of Y‐11430 (CBS7435), GS115, X‐33, and eight other variants enabled a comparative assessment of the relative fitness of these hosts for recombinant protein expression. Cell wall integrity explained the majority of the variation among strains, impacting transformation efficiency, growth, methanol metabolism, and secretion of heterologous proteins. Y‐11430 exhibited the highest activity of genes involved in methanol utilization, up to two‐fold higher transcription of heterologous genes, and robust growth. With a more permeable cell wall, X‐33 displayed a six‐fold higher transformation efficiency and up to 1.2‐fold higher titers than Y‐11430. X‐33 also shared nearly all mutations, and a defective variant of HIS4, with GS115, precluding robust growth. Transferring two beneficial mutations identified in X‐33 into Y‐11430 resulted in an optimized base strain that provided up to four‐fold higher transformation efficiency and three‐fold higher protein titers, while retaining robust growth. The approach employed here to assess unique banked variants in a species and then transfer key beneficial variants into a base strain should also facilitate rational assessment of a broad set of other recombinant hosts.
Pichia pastoris is a common host for the production of biologics and enzymes, due to fast growth, high productivity, and advancements in host engineering. The authors assessed several P. pastoris variants for relative fitness as recombinant hosts by performing genomic, transcriptomic, and phenotypic analyses on each variant. This genome‐scale approach revealed key beneficial features, which were combined to create a novel, optimized base strain.</abstract><cop>HOBOKEN</cop><pub>Wiley</pub><pmid>31654411</pmid><doi>10.1002/bit.27209</doi><tpages>13</tpages><orcidid>https://orcid.org/0000-0002-2284-3872</orcidid><orcidid>https://orcid.org/0000-0002-2400-0094</orcidid><orcidid>https://orcid.org/0000-0001-7163-9547</orcidid><orcidid>https://orcid.org/0000-0002-7912-0309</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Biotechnology & Applied Microbiology Cell walls Efficiency Fungal Proteins - genetics Fungal Proteins - metabolism Gene Expression Profiling Genes Genetic transformation Genome, Fungal - genetics Genomes Genomics heterologous gene expression Life Sciences & Biomedicine Metabolism Methanol Mutation Pichia - genetics Pichia - metabolism Pichia pastoris Protein folding Proteins recombinant protein Recombinant Proteins - genetics Recombinant Proteins - metabolism RNA, Fungal - analysis RNA, Fungal - genetics RNA‐Seq Robustness Saccharomycetales - genetics Saccharomycetales - metabolism Science & Technology Sequence Analysis, RNA Transcription Transcriptome - genetics Transformations yeast |
title | Comparative genome‐scale analysis of Pichia pastoris variants informs selection of an optimal base strain |
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