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Development of bicistronic expression system for the enhanced and reliable production of recombinant proteins in Leuconostoc citreum
The lactic acid bacteria (LAB) Leuconostoc citreum are non-sporulating hetero-fermentative bacteria that play an important role in the fermented food industry. In this study, for the enhanced and reliable production of recombinant proteins in L . citreum , we developed a bicistronic design (BCD) exp...
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Published in: | Scientific reports 2018-06, Vol.8 (1), p.8852-11, Article 8852 |
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description | The lactic acid bacteria (LAB)
Leuconostoc citreum
are non-sporulating hetero-fermentative bacteria that play an important role in the fermented food industry. In this study, for the enhanced and reliable production of recombinant proteins in
L
.
citreum
, we developed a bicistronic design (BCD) expression system which includes a short leader peptide (1
st
cistron) followed by target genes (2
nd
cistron) under the control of a single promoter. Using superfolder green fluorescent protein (sfGFP) as a reporter, the functionality of BCD in
L
.
citreum
was verified. Further, to improve the expression in BCD, we tried to engineer a Shine-Dalgarno sequence (SD2) for the 2
nd
cistron and a promoter by FACS screening of random libraries, and both strong SD2 (eSD2) and promoter (P
710V4
) were successfully isolated. The usefulness of the engineered BCD with P
710V4
and eSD2 was further validated using three model proteins—glutathione-s-transferase, human growth hormone, and α-amylase. All examined proteins were successfully produced with levels highly increased compared with those in the original BCD as well as the monocistronic design (MCD) expression system. |
doi_str_mv | 10.1038/s41598-018-27091-z |
format | article |
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Leuconostoc citreum
are non-sporulating hetero-fermentative bacteria that play an important role in the fermented food industry. In this study, for the enhanced and reliable production of recombinant proteins in
L
.
citreum
, we developed a bicistronic design (BCD) expression system which includes a short leader peptide (1
st
cistron) followed by target genes (2
nd
cistron) under the control of a single promoter. Using superfolder green fluorescent protein (sfGFP) as a reporter, the functionality of BCD in
L
.
citreum
was verified. Further, to improve the expression in BCD, we tried to engineer a Shine-Dalgarno sequence (SD2) for the 2
nd
cistron and a promoter by FACS screening of random libraries, and both strong SD2 (eSD2) and promoter (P
710V4
) were successfully isolated. The usefulness of the engineered BCD with P
710V4
and eSD2 was further validated using three model proteins—glutathione-s-transferase, human growth hormone, and α-amylase. All examined proteins were successfully produced with levels highly increased compared with those in the original BCD as well as the monocistronic design (MCD) expression system.</description><identifier>ISSN: 2045-2322</identifier><identifier>EISSN: 2045-2322</identifier><identifier>DOI: 10.1038/s41598-018-27091-z</identifier><identifier>PMID: 29891982</identifier><language>eng</language><publisher>London: Nature Publishing Group UK</publisher><subject>631/553/2698 ; 631/61/185 ; Bacteria ; Fermented food ; Flow cytometry ; Food industry ; Glutathione transferase ; Green fluorescent protein ; Growth hormones ; Humanities and Social Sciences ; Lactic acid ; Lactic acid bacteria ; multidisciplinary ; Protein sorting signals ; Proteins ; Science ; Science (multidisciplinary) ; α-Amylase</subject><ispartof>Scientific reports, 2018-06, Vol.8 (1), p.8852-11, Article 8852</ispartof><rights>The Author(s) 2018</rights><rights>2018. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c511t-2f0060193fdcf8b51be2c0f44297e33148ee1896aba3031a014e1c2efc115de43</citedby><cites>FETCH-LOGICAL-c511t-2f0060193fdcf8b51be2c0f44297e33148ee1896aba3031a014e1c2efc115de43</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/2053312903/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2053312903?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,25731,27901,27902,36989,36990,44566,53766,53768,75096</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/29891982$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Jang, Seung Hoon</creatorcontrib><creatorcontrib>Cha, Ji Won</creatorcontrib><creatorcontrib>Han, Nam Soo</creatorcontrib><creatorcontrib>Jeong, Ki Jun</creatorcontrib><title>Development of bicistronic expression system for the enhanced and reliable production of recombinant proteins in Leuconostoc citreum</title><title>Scientific reports</title><addtitle>Sci Rep</addtitle><addtitle>Sci Rep</addtitle><description>The lactic acid bacteria (LAB)
Leuconostoc citreum
are non-sporulating hetero-fermentative bacteria that play an important role in the fermented food industry. In this study, for the enhanced and reliable production of recombinant proteins in
L
.
citreum
, we developed a bicistronic design (BCD) expression system which includes a short leader peptide (1
st
cistron) followed by target genes (2
nd
cistron) under the control of a single promoter. Using superfolder green fluorescent protein (sfGFP) as a reporter, the functionality of BCD in
L
.
citreum
was verified. Further, to improve the expression in BCD, we tried to engineer a Shine-Dalgarno sequence (SD2) for the 2
nd
cistron and a promoter by FACS screening of random libraries, and both strong SD2 (eSD2) and promoter (P
710V4
) were successfully isolated. The usefulness of the engineered BCD with P
710V4
and eSD2 was further validated using three model proteins—glutathione-s-transferase, human growth hormone, and α-amylase. 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Cha, Ji Won ; Han, Nam Soo ; Jeong, Ki Jun</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c511t-2f0060193fdcf8b51be2c0f44297e33148ee1896aba3031a014e1c2efc115de43</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>631/553/2698</topic><topic>631/61/185</topic><topic>Bacteria</topic><topic>Fermented food</topic><topic>Flow cytometry</topic><topic>Food industry</topic><topic>Glutathione transferase</topic><topic>Green fluorescent protein</topic><topic>Growth hormones</topic><topic>Humanities and Social Sciences</topic><topic>Lactic acid</topic><topic>Lactic acid bacteria</topic><topic>multidisciplinary</topic><topic>Protein sorting signals</topic><topic>Proteins</topic><topic>Science</topic><topic>Science (multidisciplinary)</topic><topic>α-Amylase</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Jang, Seung Hoon</creatorcontrib><creatorcontrib>Cha, Ji Won</creatorcontrib><creatorcontrib>Han, Nam Soo</creatorcontrib><creatorcontrib>Jeong, Ki Jun</creatorcontrib><collection>Springer Open Access</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>ProQuest Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Biology Database (Alumni Edition)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Science Database (Alumni Edition)</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest One Sustainability</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>ProQuest Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Biological Sciences</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>PML(ProQuest Medical Library)</collection><collection>ProQuest Science Journals</collection><collection>Biological Science Database</collection><collection>Publicly Available Content (ProQuest)</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Scientific reports</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Jang, Seung Hoon</au><au>Cha, Ji Won</au><au>Han, Nam Soo</au><au>Jeong, Ki Jun</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Development of bicistronic expression system for the enhanced and reliable production of recombinant proteins in Leuconostoc citreum</atitle><jtitle>Scientific reports</jtitle><stitle>Sci Rep</stitle><addtitle>Sci Rep</addtitle><date>2018-06-11</date><risdate>2018</risdate><volume>8</volume><issue>1</issue><spage>8852</spage><epage>11</epage><pages>8852-11</pages><artnum>8852</artnum><issn>2045-2322</issn><eissn>2045-2322</eissn><abstract>The lactic acid bacteria (LAB)
Leuconostoc citreum
are non-sporulating hetero-fermentative bacteria that play an important role in the fermented food industry. In this study, for the enhanced and reliable production of recombinant proteins in
L
.
citreum
, we developed a bicistronic design (BCD) expression system which includes a short leader peptide (1
st
cistron) followed by target genes (2
nd
cistron) under the control of a single promoter. Using superfolder green fluorescent protein (sfGFP) as a reporter, the functionality of BCD in
L
.
citreum
was verified. Further, to improve the expression in BCD, we tried to engineer a Shine-Dalgarno sequence (SD2) for the 2
nd
cistron and a promoter by FACS screening of random libraries, and both strong SD2 (eSD2) and promoter (P
710V4
) were successfully isolated. The usefulness of the engineered BCD with P
710V4
and eSD2 was further validated using three model proteins—glutathione-s-transferase, human growth hormone, and α-amylase. All examined proteins were successfully produced with levels highly increased compared with those in the original BCD as well as the monocistronic design (MCD) expression system.</abstract><cop>London</cop><pub>Nature Publishing Group UK</pub><pmid>29891982</pmid><doi>10.1038/s41598-018-27091-z</doi><tpages>11</tpages><oa>free_for_read</oa></addata></record> |
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source | PubMed Central (Open Access); Full-Text Journals in Chemistry (Open access); Publicly Available Content (ProQuest); Springer Nature - nature.com Journals - Fully Open Access |
subjects | 631/553/2698 631/61/185 Bacteria Fermented food Flow cytometry Food industry Glutathione transferase Green fluorescent protein Growth hormones Humanities and Social Sciences Lactic acid Lactic acid bacteria multidisciplinary Protein sorting signals Proteins Science Science (multidisciplinary) α-Amylase |
title | Development of bicistronic expression system for the enhanced and reliable production of recombinant proteins in Leuconostoc citreum |
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