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...
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Veröffentlicht in: | Process biochemistry (1991) 2006-06, Vol.41 (6), p.1359-1363 |
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container_title | Process biochemistry (1991) |
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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 |
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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 & 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> |
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issn | 1359-5113 1873-3298 |
language | eng |
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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 |
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