Statistical optimization of bioluminescence of Photobacterium phosphoreum KCTC2852
In this study, media optimization by statistically designed experiments stimulated an increase in the intensity and stability of bioluminescence of Photobacterium phosphoreum KCTC 2852 during continuous cultivation. The Plackett-Burman design method selected two components (NaCl, yeast extract) amon...
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Veröffentlicht in: | Journal of bioscience and bioengineering 2001, Vol.92 (1), p.72-76 |
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container_title | Journal of bioscience and bioengineering |
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creator | Lee, Baek-Seok Lee, Jeong-Gun Shin, Dong-Hoon Kim, Eun-Ki |
description | In this study, media optimization by statistically designed experiments stimulated an increase in the intensity and stability of bioluminescence of
Photobacterium phosphoreum KCTC 2852 during continuous cultivation. The Plackett-Burman design method selected two components (NaCl, yeast extract) among nine components of the seawater complete (SC) medium. The response-surface design method calculated the optimum concentration of NaCl (31.1 g/
l) and yeast extract (5.1 g/
l). In the optimized medium, bioluminescence per cell increased twofold. During continuous cultivation in a stirred tank reactor, bioluminescence decreased rapidly in the SC medium, whereas the optimized medium could maintain bioluminescence for more than 80 h, resulting in an increased bioluminescence. Upon contact with 0.1 ppm Hg
2+, a sharp decrease in bioluminescence was observed, which was reproducible in the measuring chamber. This shows the possibility that
P. phosphoreum could be cultivated continuously with enhanced bioluminescence stability and that on-line water toxicity could be monitored continuously. |
doi_str_mv | 10.1016/S1389-1723(01)80202-4 |
format | Article |
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Photobacterium phosphoreum KCTC 2852 during continuous cultivation. The Plackett-Burman design method selected two components (NaCl, yeast extract) among nine components of the seawater complete (SC) medium. The response-surface design method calculated the optimum concentration of NaCl (31.1 g/
l) and yeast extract (5.1 g/
l). In the optimized medium, bioluminescence per cell increased twofold. During continuous cultivation in a stirred tank reactor, bioluminescence decreased rapidly in the SC medium, whereas the optimized medium could maintain bioluminescence for more than 80 h, resulting in an increased bioluminescence. Upon contact with 0.1 ppm Hg
2+, a sharp decrease in bioluminescence was observed, which was reproducible in the measuring chamber. This shows the possibility that
P. phosphoreum could be cultivated continuously with enhanced bioluminescence stability and that on-line water toxicity could be monitored continuously.</description><identifier>ISSN: 1389-1723</identifier><identifier>EISSN: 1347-4421</identifier><identifier>DOI: 10.1016/S1389-1723(01)80202-4</identifier><identifier>PMID: 16233061</identifier><identifier>CODEN: JFBIEX</identifier><language>eng</language><publisher>Amsterdarm: Elsevier B.V</publisher><subject>BACTERIA ; Biological and medical sciences ; bioluminescence ; Biotechnology ; experimental design ; Fundamental and applied biological sciences. Psychology ; LUMINESCENCE ; medium optimization ; Methods. Procedures. Technologies ; Microbial engineering. Fermentation and microbial culture technology ; OPTIMIZATION METHODS</subject><ispartof>Journal of bioscience and bioengineering, 2001, Vol.92 (1), p.72-76</ispartof><rights>2001</rights><rights>2002 INIST-CNRS</rights><rights>Copyright Japan Science and Technology Agency 2001</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4101-d0e2727962989501de5b29e0648c15f91deeda75a8f6e0b6b2db89e739bdd7903</citedby><cites>FETCH-LOGICAL-c4101-d0e2727962989501de5b29e0648c15f91deeda75a8f6e0b6b2db89e739bdd7903</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/S1389-1723(01)80202-4$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,777,781,3537,4010,27904,27905,27906,45976</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=14131187$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/16233061$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Lee, Baek-Seok</creatorcontrib><creatorcontrib>Lee, Jeong-Gun</creatorcontrib><creatorcontrib>Shin, Dong-Hoon</creatorcontrib><creatorcontrib>Kim, Eun-Ki</creatorcontrib><title>Statistical optimization of bioluminescence of Photobacterium phosphoreum KCTC2852</title><title>Journal of bioscience and bioengineering</title><addtitle>J Biosci Bioeng</addtitle><description>In this study, media optimization by statistically designed experiments stimulated an increase in the intensity and stability of bioluminescence of
Photobacterium phosphoreum KCTC 2852 during continuous cultivation. The Plackett-Burman design method selected two components (NaCl, yeast extract) among nine components of the seawater complete (SC) medium. The response-surface design method calculated the optimum concentration of NaCl (31.1 g/
l) and yeast extract (5.1 g/
l). In the optimized medium, bioluminescence per cell increased twofold. During continuous cultivation in a stirred tank reactor, bioluminescence decreased rapidly in the SC medium, whereas the optimized medium could maintain bioluminescence for more than 80 h, resulting in an increased bioluminescence. Upon contact with 0.1 ppm Hg
2+, a sharp decrease in bioluminescence was observed, which was reproducible in the measuring chamber. This shows the possibility that
P. phosphoreum could be cultivated continuously with enhanced bioluminescence stability and that on-line water toxicity could be monitored continuously.</description><subject>BACTERIA</subject><subject>Biological and medical sciences</subject><subject>bioluminescence</subject><subject>Biotechnology</subject><subject>experimental design</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>LUMINESCENCE</subject><subject>medium optimization</subject><subject>Methods. Procedures. Technologies</subject><subject>Microbial engineering. Fermentation and microbial culture technology</subject><subject>OPTIMIZATION METHODS</subject><issn>1389-1723</issn><issn>1347-4421</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2001</creationdate><recordtype>article</recordtype><recordid>eNqFkV1rFTEQhoMotj36EyoHxKIXqzNJdpNciRz8LlhsvQ7ZJGtTdjenya6gv95sz0LBGy9ChplnJu-8IeQU4TUCNm8ukUlVoaDsJeArCRRoxR-QY2RcVJxTfLjEK3JETnK-AUABAh-TI2woY9DgMfl-OZkp5ClY02_jfgpD-FMScdzGbtuG2M9DGH22frR-SV1cxym2xk4-hXnY7q9jLif5En_dXe2orOkT8qgzffZP13tDfnx4f7X7VJ1_-_h59-68srxsUDnwVFChGqqkqgGdr1uqPDRcWqw7VRLeGVEb2TUe2qalrpXKC6Za54QCtiFnh7n7FG9nnyc9hCK0783o45w1yloxLusCPv8HvIlzGos2jZwjYxKKHxtSHyibYs7Jd3qfwmDSb42gF8v1neV68VMD6jvLNS99z9bpczt4d9-1elyAFytgcnG5S2a0Id9zRQGiFIU7PXCdidr8TIX5ckGhPAOlvqzx9lD3xdRfwSedbVj-xYXk7aRdDP-R-hfnY6TV</recordid><startdate>2001</startdate><enddate>2001</enddate><creator>Lee, Baek-Seok</creator><creator>Lee, Jeong-Gun</creator><creator>Shin, Dong-Hoon</creator><creator>Kim, Eun-Ki</creator><general>Elsevier B.V</general><general>Elsevier Science</general><general>Elsevier Limited</general><scope>FBQ</scope><scope>IQODW</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QO</scope><scope>7T7</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>P64</scope></search><sort><creationdate>2001</creationdate><title>Statistical optimization of bioluminescence of Photobacterium phosphoreum KCTC2852</title><author>Lee, Baek-Seok ; Lee, Jeong-Gun ; Shin, Dong-Hoon ; Kim, Eun-Ki</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4101-d0e2727962989501de5b29e0648c15f91deeda75a8f6e0b6b2db89e739bdd7903</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2001</creationdate><topic>BACTERIA</topic><topic>Biological and medical sciences</topic><topic>bioluminescence</topic><topic>Biotechnology</topic><topic>experimental design</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>LUMINESCENCE</topic><topic>medium optimization</topic><topic>Methods. Procedures. Technologies</topic><topic>Microbial engineering. Fermentation and microbial culture technology</topic><topic>OPTIMIZATION METHODS</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Lee, Baek-Seok</creatorcontrib><creatorcontrib>Lee, Jeong-Gun</creatorcontrib><creatorcontrib>Shin, Dong-Hoon</creatorcontrib><creatorcontrib>Kim, Eun-Ki</creatorcontrib><collection>AGRIS</collection><collection>Pascal-Francis</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Biotechnology Research Abstracts</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><jtitle>Journal of bioscience and bioengineering</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Lee, Baek-Seok</au><au>Lee, Jeong-Gun</au><au>Shin, Dong-Hoon</au><au>Kim, Eun-Ki</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Statistical optimization of bioluminescence of Photobacterium phosphoreum KCTC2852</atitle><jtitle>Journal of bioscience and bioengineering</jtitle><addtitle>J Biosci Bioeng</addtitle><date>2001</date><risdate>2001</risdate><volume>92</volume><issue>1</issue><spage>72</spage><epage>76</epage><pages>72-76</pages><issn>1389-1723</issn><eissn>1347-4421</eissn><coden>JFBIEX</coden><abstract>In this study, media optimization by statistically designed experiments stimulated an increase in the intensity and stability of bioluminescence of
Photobacterium phosphoreum KCTC 2852 during continuous cultivation. The Plackett-Burman design method selected two components (NaCl, yeast extract) among nine components of the seawater complete (SC) medium. The response-surface design method calculated the optimum concentration of NaCl (31.1 g/
l) and yeast extract (5.1 g/
l). In the optimized medium, bioluminescence per cell increased twofold. During continuous cultivation in a stirred tank reactor, bioluminescence decreased rapidly in the SC medium, whereas the optimized medium could maintain bioluminescence for more than 80 h, resulting in an increased bioluminescence. Upon contact with 0.1 ppm Hg
2+, a sharp decrease in bioluminescence was observed, which was reproducible in the measuring chamber. This shows the possibility that
P. phosphoreum could be cultivated continuously with enhanced bioluminescence stability and that on-line water toxicity could be monitored continuously.</abstract><cop>Amsterdarm</cop><pub>Elsevier B.V</pub><pmid>16233061</pmid><doi>10.1016/S1389-1723(01)80202-4</doi><tpages>5</tpages></addata></record> |
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subjects | BACTERIA Biological and medical sciences bioluminescence Biotechnology experimental design Fundamental and applied biological sciences. Psychology LUMINESCENCE medium optimization Methods. Procedures. Technologies Microbial engineering. Fermentation and microbial culture technology OPTIMIZATION METHODS |
title | Statistical optimization of bioluminescence of Photobacterium phosphoreum KCTC2852 |
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