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Special Report                                                                   Special Report


 expression model. A whole-cell biocon-  ketoreductase from Lactobacillus kefi ri.  Enzyme-immobilised metal   effi ciency.  The  biotransformation  was  Biocatalytic formal regio-   of JMW’s contributions. This problem
 version system was designed and 20.89-  With improvements the conversion   organic frameworks (MOFs)  with recombinant  Pseudomonas tai-  and enantio-selective Marko-  has been solved by different process
 gm ALA was obtained from 42.42-gm  was taken to 94.3% and the concentra-  wanensis VLB120 and yield up to 61%   vnikov hydroamination of   methods, which are covered in this
 glutamate with a conversion of 63.51%.  tion of the feed could be raised from  MOFs  have  extremely  high  specifi c   is reported. (Green Chem., 2023; DOI:   aryl alkenes to chiral amines  review, with the development of enzy-
 (Catalysis Sci. Technol., 2023; DOI:  5 to 85-gm per litre. The fi nal product  surface area and adjustable porosity   10.1039/D3GC01105D).  matic  cascades.  Now the new bottle-
 10.1039/D2CY02172B).  had  an  ee of 99.9%+ and  90% yield  and these provide advantages to carry   Q. Jin et al have referred to the impor-  neck is the downstream processing and
 over two steps. Scale-up was done at 30  enzymes and to protect the activity of   Crystallisation-based down-  tance of enantiomeric  pure amines as  this is the key challenge for scale-up.
 Sustainable setups for the   litre scale. (Org. Proc. Res. Dev., 2023;  enzymes. These MOFs provide a large   stream processing of omega-  crucial intermediates for a wide range  (ChemCatChem., 2023; DOI: 10.1002/
 biocatalytic production and   DOI: 10.1021/acsoprd.2c00371).  space to carry enzymes and stabilise   transaminase- and amine   of  pharmaceuticals, natural products,  cctc.202300560).
 scale-up of panthenyl mono-  them. Further, selective mass transfer   dehydrogenase-catalysed   and bioactive compounds.  The title
 acyl esters (PMAE) under   Biocatalytic and chemo-enzy-  of substrates is provided to facilitate   reactions  process is atom-economical. The pro-  Continuous fl ow-mode syn-
 solvent-free conditions  matic synthesis of quinolines   catalytic processes.  This review   cess carries out sequential  alkene  thesis of (chiral) amines with
 (Qs) and 2-quinolones (QL) by  covers preparation strategies and pros-  asymmetric  hydration catalysed by a  transaminase (T)
 S. Nieto et al have reported a sustainable   monoamine oxidase (MAO-N)   pects and current challenges are dis-  F.  Belov  et al have referred to the   hydratase (HD),  followed by  in situ
 scaling-up process of new title bioactive   and horseradish peroxidase   cussed. (Chemistry – An Asian Jl., 17,   formation  of co-products  in the  title   oxidation of alcohol into ketone by two   H.M. Arango et al have referred to the
 provitamin-B monoacyl esters and that   (HRP) biocatalysts  issue  21/e202200751;  DOI:10.1021/  reactions, resulting in additional effort   enantio-complementary  alcohol dehydro-  essentiality of chiral amines as building
 5
 too under solvent-free conditions. This   asia.202200751).  during  downstream  processing.  Thus,   genases  (ADHs),  and  fi nally,  enantio-  blocks for a plethora of valuable com-
 is based on the formation of eutectic  H. Xiang  et al have reported that for   the removal of the residual amine donor   selective transformation of ketone into   pounds, including APIs. It seems that
 mixtures between neat substrates for  the title group of compounds the syn-  In situ product recovery of   enantiomerically  pure amine  by an   about half of the current APIs contain
 highly  effi cient  direct  esterifi cation  of  thetic methodologies still require toxic  β-ionone (BI) from fermenta-  omega-transaminase (TA). One example   chiral amines. Biocatalytic routes have
 free fatty acids, C-6 to C-18, with pan-  and expensive reagents as well as harsh  tion broth  given is that of 4-hydroxystrenes.
 thenol catalysed by lipase. 63% yield of  conditions. Two  enzymatic  strategies   Eventually,  preparative experiments
 butyrate ester is reported; it is 83% for  for the oxidation of 1,2,3,4-tetrahydro-  A.F. Arroya-Avirama et al have referred   were demonstrated by using the whole-
 myristate. A vacuum system was cou-  quinolines (THQs)  and  N-cyclopro-  to the production of BI through fermen-  cell biocatalyst E. coli (RFM-ERR-CB)
 pled to the reaction unit. The recovery  pyl-N-alkylanilines  into Qs  and QL,   tation and its recovery; genetically modi-  and E. coli (RFC-ERR-CB) with some
 and reuse of the immobilised enzyme is  respectively are described. (ACS Catal.,   fi ed  Saccharomyces cerevisiae is used.   substrates. (Green Chem., 2023; DOI:
 reported. (ACS Sustainable Chem. Eng.,  2023; DOI: 10.1021/acscatal.2c05902).  Since BI is toxic to the enzyme an in situ   10.1039/D3GC01030A).
 2023, 11, 5737-5747; DOI: 10.1021/acs-  liquid-liquid extraction was carried out.   gained considerable importance (e.g.,
 suschemeng.3c00266).  Supramolecular ionic liquid   6012 solvents were screened and looked   Scale-up of in vitro transami-  for sitagliptin, atorvastatin, etc.). Batch
 (SMIL) gels for enzyme   for partition coeffi cients using COSMO-  nase (T)-catalysed asymmetric   reactors face many problems such as
 Biocatalytic asymmetric   entrapment  RS.  The best solvents were selected   synthesis of chiral amines  catalyst separation, recovery and reuse,
 reduction of a sterically hin-  taking  into  considered  all  the  relevant   [This column has covered many papers  apart from thermodynamic restrictions.
 dered α-bromo ketone for the   H.T. Imam et al have reported a method  aspects. Further simulation was done on   based on T, which are relevant in indus-  Heterogenised biocatalysts are more
 synthesis of key intermediates   that does not require the formation of  Aspen Plus V10. Recovery was through   trial practice.]  versatile,  more stable and amenable
 of olodaterol  new covalent  bonds. SMIL gels are  two distillation columns in series. (ACS   to  continuous  fl ow  process.  Improve-
 formed containing enzymes that can  Sustainable Chem. Eng., 2023; DOI:   J.O. Madsen and  J.M.  Woodley  (who   ments in this direction  are discussed.
 Y. Feng  et al  have  reported  an  effi -  be shaped into gel beads, which act as  10.1021/acssuschemeng.3c01739).  has made many valuable contributions   (Reaction Chem. Eng., 2023; DOI:
 cient and selective biocatalytic process  recyclable immobilised  biocatalysts.   in enzymatic  processes) have referred   10.1039/D3RE00210A).
 for the reduction  of highly bulky and  The formation of gel is explained. Gel   Integrated electrosynthesis   to the unfavourable reaction equili-
 hydrophobic  α-bromo  ketone  using  entrapped lipase from Aneurinibacillus  and biosynthesis for the pro-  brium as the main bottleneck  in one   Engineering of hydroxyman-
 thermoaerophilus  was recycled  for  duction of adipic acid (AA)
 10 runs without loss of activity  and  from lignin (L) derived phe-      delate oxidase and cascade
 retained  for at  least  150 days. (ACS  nols                            reactions for high-yielding
 Sustainable Chem.  Eng.,  2023; DOI:  [This column has covered several   conversion of racemic man-
 10.1021/acssuschemeng.3c00517).  papers on valorising L to give value-  or unreacted substrates etc. cause pro-  delic acids to phenylglyoxylic
 added phenolic compounds.]  blems.  These  authors have  advocated       acids and (R)- and (S)-phenyl-
       selective removal of  the desired pro-                             glycines
 M.C. Morejon  et  al have  carried  out   duct  via  salt-  specifi c  crystallisation
 electrolytic hydrogenation to give cyclo-  step and thus the product amine crystal-  D-Y. Jung et al have adopted Directed
 hexanols followed by biotransforma-  lises as a product ammonium salt, which   Evolution  of  hydroxymandelate
 tion to give AA. 69% yield of cyclo-  can be fi ltered. (Reaction Chem. Eng.,   oxidase (HMO) and this was used for
 hexanol is reported at 69% coulombic   2023; DOI: 10.1039/D2RE00496H).   the (S)-enantioselective oxidation  of

 178  Chemical Weekly  May 14, 2024  Chemical Weekly  May 14, 2024                                     179


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