Enzymatic Synthesis of Aliphatic Nitriles at a Substrate Loading of up to 1.4 kg/L: A Biocatalytic Record Achieved with a Heme Protein

A biocatalytic approach toward linear aliphatic nitriles being widely used as industrial bulk chemicals has been developed that runs at high substrate loadings of up to 1.4 kg/L as demonstrated for the synthesis of n-octanenitrile. This substrate loading is one of the highest ever reported in biocat...

Full description

Saved in:
Bibliographic Details
Published inJournal of organic chemistry Vol. 84; no. 8; pp. 4867 - 4872
Main Authors Hinzmann, Alessa, Glinski, Sylvia, Worm, Marion, Gröger, Harald
Format Journal Article
LanguageEnglish
Published United States American Chemical Society 19.04.2019
Online AccessGet full text

Cover

Loading…
Abstract A biocatalytic approach toward linear aliphatic nitriles being widely used as industrial bulk chemicals has been developed that runs at high substrate loadings of up to 1.4 kg/L as demonstrated for the synthesis of n-octanenitrile. This substrate loading is one of the highest ever reported in biocatalysis and to best of our knowledge the highest obtained for a water-immiscible product in aqueous medium. It is noteworthy that the biotransformation at such a high substrate loading was achieved by means of a metalloprotein bearing an iron-containing heme subunit in the active site. In detail, an aldoxime dehydratase from Bacillus sp. OxB-1 was used as a biocatalyst for a dehydration of aldoximes as readily available starting materials due to their easy preparation from aliphatic aldehydes through spontaneous condensation with hydroxylamine as bulk chemical. Excellent conversions toward the nitriles in the two-phase system were achieved and the products are easily separated from the reaction mixture without the need for further purification. Aliphatic nitriles are used in industry as solvents and intermediates for the production of surfactants and life sciences products.
AbstractList A biocatalytic approach toward linear aliphatic nitriles being widely used as industrial bulk chemicals has been developed that runs at high substrate loadings of up to 1.4 kg/L as demonstrated for the synthesis of n-octanenitrile. This substrate loading is one of the highest ever reported in biocatalysis and to best of our knowledge the highest obtained for a water-immiscible product in aqueous medium. It is noteworthy that the biotransformation at such a high substrate loading was achieved by means of a metalloprotein bearing an iron-containing heme subunit in the active site. In detail, an aldoxime dehydratase from Bacillus sp. OxB-1 was used as a biocatalyst for a dehydration of aldoximes as readily available starting materials due to their easy preparation from aliphatic aldehydes through spontaneous condensation with hydroxylamine as bulk chemical. Excellent conversions toward the nitriles in the two-phase system were achieved and the products are easily separated from the reaction mixture without the need for further purification. Aliphatic nitriles are used in industry as solvents and intermediates for the production of surfactants and life sciences products.
Author Gröger, Harald
Glinski, Sylvia
Worm, Marion
Hinzmann, Alessa
AuthorAffiliation Chair of Industrial Organic Chemistry and Biotechnology, Faculty of Chemistry
AuthorAffiliation_xml – name: Chair of Industrial Organic Chemistry and Biotechnology, Faculty of Chemistry
Author_xml – sequence: 1
  givenname: Alessa
  surname: Hinzmann
  fullname: Hinzmann, Alessa
– sequence: 2
  givenname: Sylvia
  surname: Glinski
  fullname: Glinski, Sylvia
– sequence: 3
  givenname: Marion
  surname: Worm
  fullname: Worm, Marion
– sequence: 4
  givenname: Harald
  orcidid: 0000-0001-8582-2107
  surname: Gröger
  fullname: Gröger, Harald
  email: harald.groeger@uni-bielefeld.de
BackLink https://www.ncbi.nlm.nih.gov/pubmed/30844280$$D View this record in MEDLINE/PubMed
BookMark eNp1kEFP2zAUgK0JNEq3827Ix0lTWj87DvZuHYKBVLFphXPkOi_UkMTFdjaVH7DfTUoLN3x5kvW9T3rfMTnofIeEfAE2AcZhamyc3Hs70UvGQOUfyAgkZ1mhWX5ARoxxngleiCNyHOM9G56U8iM5EkzlOVdsRP6fd0-b1iRn6WLTpRVGF6mv6axx69XL97VLwTUYqUnU0EW_jCmYhHTuTeW6uy3cr2nyFCY5fbibzr_TGf3hvDXJNJut4Q9aHyo6syuHf7Gi_1xaDapLbJH-Dj6h6z6Rw9o0ET_v55jcXpzfnF1m818_r85m88wIIVImVaGropYAwihxWoEUS1Exq2vUnNVMclWI06LGAqoaBNNgAHIFWukcrVViTL7uvOvgH3uMqWxdtNg0pkPfx5KD0lLoQuoBne5QG3yMAetyHVxrwqYEVm7jl0P8cohf7uMPGyd7eb9ssXrjX2sPwLcdsNvsQzfc-q7uGURCj7s
CitedBy_id crossref_primary_10_1021_acs_joc_9b02773
crossref_primary_10_1002_anie_202015887
crossref_primary_10_1002_ejlt_201900163
crossref_primary_10_1002_ange_202017234
crossref_primary_10_3390_molecules26154466
crossref_primary_10_1002_ange_202013171
crossref_primary_10_1016_j_nbt_2020_07_002
crossref_primary_10_1002_anie_202013171
crossref_primary_10_1016_j_cogsc_2019_08_006
crossref_primary_10_1002_cctc_202100835
crossref_primary_10_1002_chem_202001647
crossref_primary_10_1016_j_cogsc_2021_100514
crossref_primary_10_3390_suschem1030018
crossref_primary_10_1002_cssc_202102683
crossref_primary_10_1007_s12268_019_0093_3
crossref_primary_10_1039_D1GC00561H
crossref_primary_10_1016_j_jbiotec_2023_02_007
crossref_primary_10_1038_s41598_021_92749_0
crossref_primary_10_1039_C9NP90031D
crossref_primary_10_1002_ange_202015887
crossref_primary_10_1016_j_checat_2023_100615
crossref_primary_10_1021_acssuschemeng_0c04981
crossref_primary_10_1039_D3NP00028A
crossref_primary_10_1002_ejlt_202200177
crossref_primary_10_1002_anie_202006648
crossref_primary_10_1038_s43586_021_00044_z
crossref_primary_10_3389_fctls_2022_883161
crossref_primary_10_1016_j_jbiotec_2024_02_005
crossref_primary_10_1002_anie_202017234
crossref_primary_10_1016_j_jbiotec_2024_02_007
crossref_primary_10_1016_j_gresc_2021_04_001
crossref_primary_10_1021_acs_orglett_9b02682
crossref_primary_10_1002_ejoc_201901168
crossref_primary_10_1039_D1CY01694F
crossref_primary_10_1002_ejoc_201901365
crossref_primary_10_3390_molecules24193573
crossref_primary_10_1016_j_checat_2023_100572
crossref_primary_10_1002_ange_202006648
crossref_primary_10_1016_j_checat_2022_09_037
crossref_primary_10_1002_cssc_202200402
crossref_primary_10_3390_catal10040362
crossref_primary_10_1039_D2RA03256B
crossref_primary_10_1039_D0GC01445A
crossref_primary_10_3390_catal10091073
Cites_doi 10.1002/3527608184
10.1111/j.1574-6968.1998.tb12818.x
10.1016/S1389-1723(04)70200-5
10.1002/cbic.201700571
10.1002/cbic.200600261
10.1074/jbc.M410474200
10.1021/bi035092u
10.1016/B978-0-08-095167-6.00708-4
10.1271/bbb.65.2666
10.1073/pnas.1200338110
10.1021/bi991598u
10.1271/bbb.69.2254
10.1007/s00253-005-0044-4
10.1002/cctc.201402612
10.1002/anie.201702952
10.1016/S1381-1177(98)00080-0
10.1128/AEM.66.6.2290-2296.2000
10.1002/9783527639861
10.1016/S0168-1656(01)00419-9
ContentType Journal Article
DBID NPM
AAYXX
CITATION
7X8
DOI 10.1021/acs.joc.9b00184
DatabaseName PubMed
CrossRef
MEDLINE - Academic
DatabaseTitle PubMed
CrossRef
MEDLINE - Academic
DatabaseTitleList
PubMed
Database_xml – sequence: 1
  dbid: NPM
  name: PubMed
  url: https://proxy.k.utb.cz/login?url=http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed
  sourceTypes: Index Database
DeliveryMethod fulltext_linktorsrc
Discipline Chemistry
EISSN 1520-6904
EndPage 4872
ExternalDocumentID 10_1021_acs_joc_9b00184
30844280
c678527528
Genre Research Support, Non-U.S. Gov't
Journal Article
GroupedDBID -
.K2
29L
53G
55A
5RE
5VS
7~N
85S
AABXI
ABFLS
ABMVS
ABPPZ
ABPTK
ABUCX
ABUFD
ACGFS
ACJ
ACNCT
ACS
AEESW
AENEX
AFEFF
ALMA_UNASSIGNED_HOLDINGS
AQSVZ
BAANH
CJ0
CS3
D0L
DU5
DZ
EBS
ED
ED~
EJD
F20
F5P
GNL
IH9
IHE
JG
JG~
K2
LG6
P2P
PZZ
ROL
RXW
TAE
TN5
UI2
UKR
UPT
VF5
VG9
VQA
W1F
WH7
X
XFK
YZZ
---
-DZ
-~X
4.4
AAHBH
ABJNI
ABQRX
ACBEA
ACGFO
ADHLV
AGXLV
AHGAQ
CUPRZ
GGK
IH2
NPM
TAF
XSW
YQT
ZCA
AAYXX
CITATION
7X8
ID FETCH-LOGICAL-a333t-5869d6f5113a837d153b3d0c9fe920f05286376fe61df13091a114819894ecc83
IEDL.DBID ACS
ISSN 0022-3263
IngestDate Fri Aug 16 21:49:47 EDT 2024
Fri Aug 23 01:04:56 EDT 2024
Sat Sep 28 08:28:38 EDT 2024
Thu Aug 27 13:43:30 EDT 2020
IsPeerReviewed true
IsScholarly true
Issue 8
Language English
LinkModel DirectLink
MergedId FETCHMERGED-LOGICAL-a333t-5869d6f5113a837d153b3d0c9fe920f05286376fe61df13091a114819894ecc83
Notes ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
ORCID 0000-0001-8582-2107
PMID 30844280
PQID 2189539659
PQPubID 23479
PageCount 6
ParticipantIDs proquest_miscellaneous_2189539659
crossref_primary_10_1021_acs_joc_9b00184
pubmed_primary_30844280
acs_journals_10_1021_acs_joc_9b00184
ProviderPackageCode JG~
55A
AABXI
GNL
VF5
7~N
ACJ
VG9
W1F
ACS
AEESW
AFEFF
.K2
ABMVS
ABUCX
IH9
BAANH
AQSVZ
ED~
UI2
PublicationCentury 2000
PublicationDate 20190419
2019-04-19
PublicationDateYYYYMMDD 2019-04-19
PublicationDate_xml – month: 04
  year: 2019
  text: 20190419
  day: 19
PublicationDecade 2010
PublicationPlace United States
PublicationPlace_xml – name: United States
PublicationTitle Journal of organic chemistry
PublicationTitleAlternate J. Org. Chem
PublicationYear 2019
Publisher American Chemical Society
Publisher_xml – name: American Chemical Society
References ref9/cit9
ref17/cit17
ref6/cit6
ref10/cit10
ref18/cit18
ref19/cit19
Liese A. (ref1/cit1) 2006
ref21/cit21
ref11/cit11
ref12/cit12
ref15/cit15
ref16/cit16
ref22/cit22
ref13/cit13
ref14/cit14
ref8/cit8
ref5/cit5
Arpe H.-J. (ref2/cit2) 2010
Pollak P. (ref3/cit3) 2000
ref4/cit4
Drauz K. (ref23/cit23) 2012; 1
ref20/cit20
ref7/cit7
References_xml – volume-title: Industrial Biotransformations
  year: 2006
  ident: ref1/cit1
  doi: 10.1002/3527608184
  contributor:
    fullname: Liese A.
– ident: ref7/cit7
  doi: 10.1111/j.1574-6968.1998.tb12818.x
– ident: ref13/cit13
  doi: 10.1016/S1389-1723(04)70200-5
– ident: ref22/cit22
  doi: 10.1002/cbic.201700571
– ident: ref16/cit16
  doi: 10.1002/cbic.200600261
– ident: ref11/cit11
  doi: 10.1074/jbc.M410474200
– ident: ref14/cit14
  doi: 10.1021/bi035092u
– volume-title: Industrial Organic Chemistry
  year: 2010
  ident: ref2/cit2
  contributor:
    fullname: Arpe H.-J.
– ident: ref5/cit5
  doi: 10.1016/B978-0-08-095167-6.00708-4
– ident: ref18/cit18
  doi: 10.1271/bbb.65.2666
– ident: ref9/cit9
  doi: 10.1073/pnas.1200338110
– ident: ref10/cit10
  doi: 10.1021/bi991598u
– ident: ref12/cit12
  doi: 10.1271/bbb.69.2254
– ident: ref15/cit15
  doi: 10.1007/s00253-005-0044-4
– ident: ref19/cit19
– ident: ref20/cit20
  doi: 10.1002/cctc.201402612
– ident: ref21/cit21
  doi: 10.1002/anie.201702952
– volume-title: Ullmann’s Encyclopedia of Industrial Chemistry
  year: 2000
  ident: ref3/cit3
  contributor:
    fullname: Pollak P.
– ident: ref8/cit8
  doi: 10.1021/bi991598u
– ident: ref17/cit17
  doi: 10.1016/S1381-1177(98)00080-0
– ident: ref6/cit6
  doi: 10.1128/AEM.66.6.2290-2296.2000
– volume: 1
  volume-title: Enzyme Catalysis in Organic Synthesis
  year: 2012
  ident: ref23/cit23
  doi: 10.1002/9783527639861
  contributor:
    fullname: Drauz K.
– ident: ref4/cit4
  doi: 10.1016/S0168-1656(01)00419-9
SSID ssj0000555
Score 2.5069568
Snippet A biocatalytic approach toward linear aliphatic nitriles being widely used as industrial bulk chemicals has been developed that runs at high substrate loadings...
SourceID proquest
crossref
pubmed
acs
SourceType Aggregation Database
Index Database
Publisher
StartPage 4867
Title Enzymatic Synthesis of Aliphatic Nitriles at a Substrate Loading of up to 1.4 kg/L: A Biocatalytic Record Achieved with a Heme Protein
URI http://dx.doi.org/10.1021/acs.joc.9b00184
https://www.ncbi.nlm.nih.gov/pubmed/30844280
https://search.proquest.com/docview/2189539659
Volume 84
hasFullText 1
inHoldings 1
isFullTextHit
isPrint
link http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwjV1NT9wwELX4OMAFSmlhaYumEodeEpw4TuLe0hVohSiqRJG4RY7tQKBNViSLtPwAfnfHzu6iFqFytayRNZ7MvPFM3hBykMTcjhsoPZ2UhRcFlHkFo8YTytKhF1Qbaf8d_n4Wjy6ik0t--UQW_W8FPwwOpWr9m0b5lrwP05FlshomVNgpDdnw_Mnpcs4XxOBhzBYsPs8E2DCk2r_D0AvY0sWY482-O6t11IS2teTWn3SFrx6eEzf-__hvyMYMaULWm8YWWTL1W7I2nA942yaPR_XD1DG2wvm0RiDYVi00JWS_qvG1Wz6rujv0Gi3IDiRYH-O4bOG0cZ33dvNkDF0DgR_B7dXh6VfI4FvVuDehqZXQZ7eQqevK3BsN9tkXRY3MbwM_LEVEVb8jF8dHP4cjbzaWwZOMsc7jaSx0XCJSYxLTW40-s2CaKlEagbdOeZjG6LZKEwe6xBApAmmTLtucFaHBpOw9Wamb2uwSQLyhExnqVKoyMjEVUiSBEDLhJkVXYgbkAPWXzz6rNncV8zDI-0WVz5Q6IF_ml5mPe5KOl7d-nl92juq21RFZm2bS5oh1BGeWX3FAdnorWAhjNI0wT6N7rzvPB7KOuMoVnQLxkax0dxPzCbFLV-w7q_0DauvmYQ
link.rule.ids 315,783,787,2774,27090,27938,27939,57072,57122
linkProvider American Chemical Society
linkToHtml http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwlV1LT9wwEB5RONBLW-hr-5xKHHrJ4qzjJOaWrkBLWVatAIlb5MROSWmTFclWWn5AfzdjZ3dRi5Daq2WNHHsy841n_A3AThQK226g8HRUZF7gM-5lnBlP5pYOPWPaKPt2-HgSjs6Cz-fifA3Y8i0MLaIhSY1L4t-yC_i7dux7nfcthx9FJQ9gQ0Qssj0LkuHJre0VQqz4wQchX5H53BFgvVHe_OmN7oGYztUcPIavq0W6CpPL_qzN-vn1X_yN__MVT-DRAndi0inKFqyZahs2h8t2b0_h9351PXf8rXgyrwgWNmWDdYHJj3J64YYnZXtFNqRB1aJCa3Ecsy2Oa1eHbyfPptjW6PcDvPy2O97DBD-VtbshmlsJXayLSX5Rml9Go70EJlEj89PgF0sYUVbP4Oxg_3Q48hZNGjzFOW89EYdShwXhNq4o2NVkQTOuWS4LI0kHmBjEIRmxwoS-LshhSl_ZEMyWagWkPjF_DutVXZmXgIQ-dKQGOlZ5EZiQSSUjX0oVCROTYTE92KH9Sxc_WZO6_PnAT7vBPF1sag8-Ls80nXaUHfdP_bA885S22-ZKVGXqWZMS8pGCW7bFHrzolGEljLM4oKiNvfq39byHzdHp8TgdH06OXsNDQlwuHeXLN7DeXs3MW0I1bfbOKfIN0vzuyg
linkToPdf http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwlV1Lb9QwELagSMClPEuX8jBSD1yyjeM4iXsLS1cLLKtKZaXeIie2aWibrJos0vYH8LuZcbKLAFWCq2WN_BjPfOOxvyFkP44Elhuwno5t7oXM517OfePJAunQc18bhX-HP8-iyTz8eCpO-09h-BcGBtGApMYl8fFUL7TtGQbYAbZ_q4sh8vhBZHKb3BExC7BuQTo6-WV_hRAbjvAg4htCn78EoEcqmt890g0w07mb8QMy3wzUvTI5Hy7bfFhc_8Hh-L8zeUi2e_xJ005hHpFbpnpM7o3WZd-ekB9H1fXK8bjSk1UF8LApG1pbml6UizPXPCvbK7AlDVUtVRQtj2O4pdPavcfHzssFbWvKhiE9_3owPaQpfVfW7qZohRK6mJemxVlpvhtN8TIYRE3MpaHHSBxRVk_JfHz0ZTTx-mINnuKct55IIqkjC_iNKwh6NVjSnGu_kNZI0AVfBEkExsyaiGkLjlMyhaEYPtkKQY0SvkO2qroyu4QCCtGxCnSiChuayJdKxkxKFQuTgIExA7IP65f1h63JXB49YFnXWGT9og7I2_W-ZouOuuPmrm_W-57BcmPORFWmXjYZICApOLIuDsizTiE2wrifhBC9-c__bTyvyd3j9-Ns-mH2aY_cB-DlslJMviBb7dXSvARw0-avnC7_BJuv8UQ
openUrl ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fsummon.serialssolutions.com&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.atitle=Enzymatic+Synthesis+of+Aliphatic+Nitriles+at+a+Substrate+Loading+of+up+to+1.4+kg%2FL%3A+A+Biocatalytic+Record+Achieved+with+a+Heme+Protein&rft.jtitle=Journal+of+organic+chemistry&rft.au=Hinzmann%2C+Alessa&rft.au=Glinski%2C+Sylvia&rft.au=Worm%2C+Marion&rft.au=Gro%CC%88ger%2C+Harald&rft.date=2019-04-19&rft.pub=American+Chemical+Society&rft.issn=0022-3263&rft.eissn=1520-6904&rft.volume=84&rft.issue=8&rft.spage=4867&rft.epage=4872&rft_id=info:doi/10.1021%2Facs.joc.9b00184&rft.externalDocID=c678527528
thumbnail_l http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=0022-3263&client=summon
thumbnail_m http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=0022-3263&client=summon
thumbnail_s http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=0022-3263&client=summon