Rhodococcus rhodochrous PA-34: A potential biocatalyst for acrylamide synthesis

Rhodococcus rhodochrous PA-34 exhibited 55 U mg −1 dcw nitrile hydratase (NHase) activity for the transformation of acrylonitrile to acrylamide. The culture conditions of R. rhodochrous PA-34 for the production of NHase and reaction conditions for this NHase mediated conversion of acrylonitrile to a...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Process biochemistry (1991) 2006-06, Vol.41 (6), p.1359-1363
Hauptverfasser: Raj, Jog, Prasad, Shreenath, Bhalla, Tek Chand
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 1363
container_issue 6
container_start_page 1359
container_title Process biochemistry (1991)
container_volume 41
creator Raj, Jog
Prasad, Shreenath
Bhalla, Tek Chand
description Rhodococcus rhodochrous PA-34 exhibited 55 U mg −1 dcw nitrile hydratase (NHase) activity for the transformation of acrylonitrile to acrylamide. The culture conditions of R. rhodochrous PA-34 for the production of NHase and reaction conditions for this NHase mediated conversion of acrylonitrile to acrylamide were optimised. The maximum production of NHase (2.5 U mL −1 culture) was carried out by culturing R. rhodochrous PA-34 in the medium containing (L −1) 10.0 g glycerol, 5.0 g peptone, 3.0 g yeast extract, 20 mg CoCl 2, pH 7.0, 2 mL propionitrile at 30 °C for 36 h in an incubator shaker (160 rpm). The maximum conversion of acrylonitrile to acrylamide was observed in 100 mM potassium phosphate buffer (pH 7.0), at 10 °C, acrylonitrile (8%, w/v, i.e. 1500 mM) using resting cells of this organism corresponding to 1.6 mg dry cell weight (dcw) mL −1 reaction mixture (specific activity 55 U mg −1 dcw) in 1 h. The resting cells of R. rhodochrous PA-34 retained 76% NHase activity even in the presence of 20% (w/v) acrylonitrile. The conversion of acrylonitrile to acrylamide was carried out at 1 L scale and 600 g (8442 mM) of acrylamide was produced in 12 h at 10 °C.
doi_str_mv 10.1016/j.procbio.2006.01.022
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_29430120</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S1359511306000419</els_id><sourcerecordid>29430120</sourcerecordid><originalsourceid>FETCH-LOGICAL-c371t-62919e7cf65bc382be7bf7452bb6e69a748e4c14adb3445832f2905a3609ebcd3</originalsourceid><addsrcrecordid>eNqFkEtLAzEUhYMoWKs_QZiVuxnzmpcbKcUXFCqi65DcuUNTppOapEL_vant3tU9i3POvfcj5JbRglFW3a-LrXdgrCs4pVVBWUE5PyMT1tQiF7xtzpMWZZuXjIlLchXCmlLBGKMTsvxYuc6BA9iFzP_plXdJv89yIR-yWbZ1Ecdo9ZClDaCjHvYhZr3zmQa_H_TGdpiF_RhXGGy4Jhe9HgLenOaUfD0_fc5f88Xy5W0-W-QgahbziresxRr6qjQgGm6wNn0tS25MhVWra9mgBCZ1Z4SUZSN4z1taalHRFg10Ykrujr3p9e8dhqg2NgAOgx4xna94KwVlnCZjeTSCdyF47NXW2432e8WoOuBTa3XCpw74FGUq4Uu5x2MO0xc_Fr0KYHEE7KxHiKpz9p-GX8phfAU</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>29430120</pqid></control><display><type>article</type><title>Rhodococcus rhodochrous PA-34: A potential biocatalyst for acrylamide synthesis</title><source>Access via ScienceDirect (Elsevier)</source><creator>Raj, Jog ; Prasad, Shreenath ; Bhalla, Tek Chand</creator><creatorcontrib>Raj, Jog ; Prasad, Shreenath ; Bhalla, Tek Chand</creatorcontrib><description>Rhodococcus rhodochrous PA-34 exhibited 55 U mg −1 dcw nitrile hydratase (NHase) activity for the transformation of acrylonitrile to acrylamide. The culture conditions of R. rhodochrous PA-34 for the production of NHase and reaction conditions for this NHase mediated conversion of acrylonitrile to acrylamide were optimised. The maximum production of NHase (2.5 U mL −1 culture) was carried out by culturing R. rhodochrous PA-34 in the medium containing (L −1) 10.0 g glycerol, 5.0 g peptone, 3.0 g yeast extract, 20 mg CoCl 2, pH 7.0, 2 mL propionitrile at 30 °C for 36 h in an incubator shaker (160 rpm). The maximum conversion of acrylonitrile to acrylamide was observed in 100 mM potassium phosphate buffer (pH 7.0), at 10 °C, acrylonitrile (8%, w/v, i.e. 1500 mM) using resting cells of this organism corresponding to 1.6 mg dry cell weight (dcw) mL −1 reaction mixture (specific activity 55 U mg −1 dcw) in 1 h. The resting cells of R. rhodochrous PA-34 retained 76% NHase activity even in the presence of 20% (w/v) acrylonitrile. The conversion of acrylonitrile to acrylamide was carried out at 1 L scale and 600 g (8442 mM) of acrylamide was produced in 12 h at 10 °C.</description><identifier>ISSN: 1359-5113</identifier><identifier>EISSN: 1873-3298</identifier><identifier>DOI: 10.1016/j.procbio.2006.01.022</identifier><language>eng</language><publisher>Elsevier Ltd</publisher><subject>Acrylamide ; Acrylonitrile ; Nitrile hydratase (NHase) ; Rhodococcus rhodochrous PA-34</subject><ispartof>Process biochemistry (1991), 2006-06, Vol.41 (6), p.1359-1363</ispartof><rights>2006 Elsevier Ltd</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c371t-62919e7cf65bc382be7bf7452bb6e69a748e4c14adb3445832f2905a3609ebcd3</citedby><cites>FETCH-LOGICAL-c371t-62919e7cf65bc382be7bf7452bb6e69a748e4c14adb3445832f2905a3609ebcd3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.procbio.2006.01.022$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>315,781,785,3551,27928,27929,45999</link.rule.ids></links><search><creatorcontrib>Raj, Jog</creatorcontrib><creatorcontrib>Prasad, Shreenath</creatorcontrib><creatorcontrib>Bhalla, Tek Chand</creatorcontrib><title>Rhodococcus rhodochrous PA-34: A potential biocatalyst for acrylamide synthesis</title><title>Process biochemistry (1991)</title><description>Rhodococcus rhodochrous PA-34 exhibited 55 U mg −1 dcw nitrile hydratase (NHase) activity for the transformation of acrylonitrile to acrylamide. The culture conditions of R. rhodochrous PA-34 for the production of NHase and reaction conditions for this NHase mediated conversion of acrylonitrile to acrylamide were optimised. The maximum production of NHase (2.5 U mL −1 culture) was carried out by culturing R. rhodochrous PA-34 in the medium containing (L −1) 10.0 g glycerol, 5.0 g peptone, 3.0 g yeast extract, 20 mg CoCl 2, pH 7.0, 2 mL propionitrile at 30 °C for 36 h in an incubator shaker (160 rpm). The maximum conversion of acrylonitrile to acrylamide was observed in 100 mM potassium phosphate buffer (pH 7.0), at 10 °C, acrylonitrile (8%, w/v, i.e. 1500 mM) using resting cells of this organism corresponding to 1.6 mg dry cell weight (dcw) mL −1 reaction mixture (specific activity 55 U mg −1 dcw) in 1 h. The resting cells of R. rhodochrous PA-34 retained 76% NHase activity even in the presence of 20% (w/v) acrylonitrile. The conversion of acrylonitrile to acrylamide was carried out at 1 L scale and 600 g (8442 mM) of acrylamide was produced in 12 h at 10 °C.</description><subject>Acrylamide</subject><subject>Acrylonitrile</subject><subject>Nitrile hydratase (NHase)</subject><subject>Rhodococcus rhodochrous PA-34</subject><issn>1359-5113</issn><issn>1873-3298</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2006</creationdate><recordtype>article</recordtype><recordid>eNqFkEtLAzEUhYMoWKs_QZiVuxnzmpcbKcUXFCqi65DcuUNTppOapEL_vant3tU9i3POvfcj5JbRglFW3a-LrXdgrCs4pVVBWUE5PyMT1tQiF7xtzpMWZZuXjIlLchXCmlLBGKMTsvxYuc6BA9iFzP_plXdJv89yIR-yWbZ1Ecdo9ZClDaCjHvYhZr3zmQa_H_TGdpiF_RhXGGy4Jhe9HgLenOaUfD0_fc5f88Xy5W0-W-QgahbziresxRr6qjQgGm6wNn0tS25MhVWra9mgBCZ1Z4SUZSN4z1taalHRFg10Ykrujr3p9e8dhqg2NgAOgx4xna94KwVlnCZjeTSCdyF47NXW2432e8WoOuBTa3XCpw74FGUq4Uu5x2MO0xc_Fr0KYHEE7KxHiKpz9p-GX8phfAU</recordid><startdate>20060601</startdate><enddate>20060601</enddate><creator>Raj, Jog</creator><creator>Prasad, Shreenath</creator><creator>Bhalla, Tek Chand</creator><general>Elsevier Ltd</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7U5</scope><scope>8FD</scope><scope>F28</scope><scope>FR3</scope><scope>L7M</scope></search><sort><creationdate>20060601</creationdate><title>Rhodococcus rhodochrous PA-34: A potential biocatalyst for acrylamide synthesis</title><author>Raj, Jog ; Prasad, Shreenath ; Bhalla, Tek Chand</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c371t-62919e7cf65bc382be7bf7452bb6e69a748e4c14adb3445832f2905a3609ebcd3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2006</creationdate><topic>Acrylamide</topic><topic>Acrylonitrile</topic><topic>Nitrile hydratase (NHase)</topic><topic>Rhodococcus rhodochrous PA-34</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Raj, Jog</creatorcontrib><creatorcontrib>Prasad, Shreenath</creatorcontrib><creatorcontrib>Bhalla, Tek Chand</creatorcontrib><collection>CrossRef</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>Technology Research Database</collection><collection>ANTE: Abstracts in New Technology &amp; Engineering</collection><collection>Engineering Research Database</collection><collection>Advanced Technologies Database with Aerospace</collection><jtitle>Process biochemistry (1991)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Raj, Jog</au><au>Prasad, Shreenath</au><au>Bhalla, Tek Chand</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Rhodococcus rhodochrous PA-34: A potential biocatalyst for acrylamide synthesis</atitle><jtitle>Process biochemistry (1991)</jtitle><date>2006-06-01</date><risdate>2006</risdate><volume>41</volume><issue>6</issue><spage>1359</spage><epage>1363</epage><pages>1359-1363</pages><issn>1359-5113</issn><eissn>1873-3298</eissn><abstract>Rhodococcus rhodochrous PA-34 exhibited 55 U mg −1 dcw nitrile hydratase (NHase) activity for the transformation of acrylonitrile to acrylamide. The culture conditions of R. rhodochrous PA-34 for the production of NHase and reaction conditions for this NHase mediated conversion of acrylonitrile to acrylamide were optimised. The maximum production of NHase (2.5 U mL −1 culture) was carried out by culturing R. rhodochrous PA-34 in the medium containing (L −1) 10.0 g glycerol, 5.0 g peptone, 3.0 g yeast extract, 20 mg CoCl 2, pH 7.0, 2 mL propionitrile at 30 °C for 36 h in an incubator shaker (160 rpm). The maximum conversion of acrylonitrile to acrylamide was observed in 100 mM potassium phosphate buffer (pH 7.0), at 10 °C, acrylonitrile (8%, w/v, i.e. 1500 mM) using resting cells of this organism corresponding to 1.6 mg dry cell weight (dcw) mL −1 reaction mixture (specific activity 55 U mg −1 dcw) in 1 h. The resting cells of R. rhodochrous PA-34 retained 76% NHase activity even in the presence of 20% (w/v) acrylonitrile. The conversion of acrylonitrile to acrylamide was carried out at 1 L scale and 600 g (8442 mM) of acrylamide was produced in 12 h at 10 °C.</abstract><pub>Elsevier Ltd</pub><doi>10.1016/j.procbio.2006.01.022</doi><tpages>5</tpages></addata></record>
fulltext fulltext
identifier ISSN: 1359-5113
ispartof Process biochemistry (1991), 2006-06, Vol.41 (6), p.1359-1363
issn 1359-5113
1873-3298
language eng
recordid cdi_proquest_miscellaneous_29430120
source Access via ScienceDirect (Elsevier)
subjects Acrylamide
Acrylonitrile
Nitrile hydratase (NHase)
Rhodococcus rhodochrous PA-34
title Rhodococcus rhodochrous PA-34: A potential biocatalyst for acrylamide synthesis
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-16T16%3A53%3A45IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Rhodococcus%20rhodochrous%20PA-34:%20A%20potential%20biocatalyst%20for%20acrylamide%20synthesis&rft.jtitle=Process%20biochemistry%20(1991)&rft.au=Raj,%20Jog&rft.date=2006-06-01&rft.volume=41&rft.issue=6&rft.spage=1359&rft.epage=1363&rft.pages=1359-1363&rft.issn=1359-5113&rft.eissn=1873-3298&rft_id=info:doi/10.1016/j.procbio.2006.01.022&rft_dat=%3Cproquest_cross%3E29430120%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=29430120&rft_id=info:pmid/&rft_els_id=S1359511306000419&rfr_iscdi=true