scholarly journals Production of Glucose 6-Phosphate From a Cellulosic Feedstock in a One Pot Multi-Enzyme Synthesis

Author(s):  
Anne Usvalampi ◽  
He Li ◽  
Alexander D. Frey

Glucose 6-phosphate is the phosphorylated form of glucose and is used as a reagent in enzymatic assays. Current production occurs via a multi-step chemical synthesis. In this study we established a fully enzymatic route for the synthesis of glucose 6-phosphate from cellulose. As the enzymatic phosphorylation requires ATP as phosphoryl donor, the use of a cofactor regeneration system is required. We evaluated Escherichia coli glucokinase and Saccharomyces cerevisiae hexokinase (HK) for the phosphorylation reaction and Pseudomonas aeruginosa polyphosphate kinase 2 (PPK2) for ATP regeneration. All three enzymes were characterized in terms of temperature and pH optimum and the effects of substrates and products concentrations on enzymatic activities. After optimization of the conditions, we achieved a 85% conversion of glucose into glucose 6-phosphate using the HK/PPK2 activities within a 24 h reaction resulting in 12.56 g/l of glucose 6-phosphate. Finally, we demonstrated the glucose 6-phosphate formation from microcrystalline cellulose in a one-pot reaction comprising Aspergillus niger cellulase for glucose release and HK/PPK2 activities. We achieved a 77% conversion of released glucose into glucose 6-phosphate, however at the expense of a lower glucose 6-phosphate yield of 1.17 g/l. Overall, our study shows an alternative approach for synthesis of glucose 6-phosphate that can be used to valorize biomass derived cellulose.

SynOpen ◽  
2021 ◽  
Author(s):  
Valerio Zullo ◽  
Antonella Petri ◽  
Anna Iuliano

The synthesis of 6-aminoisomannide is easily achieved starting from the renewable, inexpensive and commercially available isosorbide, in 66% overall yield. A biocatalysed highly regioselective acetylation of the 3-endo hydroxyl group of isosorbide was followed by the stereospecific interconversion of the 6-exo hydroxyl group into azido group, through reaction with trifluoromethanesulfonic anhydride followed by nucleophilic displacement of the triflate group by sodium azide. Finally, reduction of the azido group and deacetylation of the 3-hydroxy group were performed one pot by using LiAlH4.


1975 ◽  
Vol 21 (12) ◽  
pp. 2028-2033
Author(s):  
Prince K. Zachariah ◽  
John Liston

A psychrotrophic pseudomonad isolated from iced fish oxidized alanine at temperatures close to 0 °C and grew over the range 0 °C–35 °C. The rate of oxidation of alanine, measured manometrically, by cells grown at 2 °C was lower than that of cells grown at 22 °C. However, the consumption of oxygen after heat treatment at 35 °C for 35 min was reduced considerably by 2 °C grown cells. Alanine oxidase activity was tested in an extract from cells grown at 2 °C and 22 °C with alanine as the sole carbon, nitrogen, and energy source. Cells grown at 2 °C produced an alanine oxidase with a temperature optimum of 35 °C and pH optimum of 8, which lost about 80% activity by heat treatment at 40 °C for 30 min. There was no change in activity after dialysis at pH 7, 8, or 9. Extracts from cells grown at 22 °C contained an alanine oxidase system with an optimum temperature of 45 °C, a pH optimum above 8, and only about 30% reduction of activity after heat treatment. This enzyme activity was concentrated in the 0.5 M elution fraction from a Sephadex column, and dialysis reduced the activity at pH 7 and 8. Mesophilic enzyme synthesis apparently started around a growth temperature of 10 °C.The crude alanine oxidase systems of Pseudomonas aeruginosa derived from cells grown at 13 °C and 37 °C had a common optimum temperature of 45 °C. These data suggest that one mechanism of psychrophilic growth by psychrotrophic bacteria may be the induction of enzymes with low optimum temperatures in response to low temperature conditions.


2010 ◽  
Vol 48 (23) ◽  
pp. 5289-5297 ◽  
Author(s):  
Magnus Eriksson ◽  
Antoine Boyer ◽  
Loris Sinigoi ◽  
Mats Johansson ◽  
Eva Malmström ◽  
...  
Keyword(s):  
One Pot ◽  

2001 ◽  
Vol 66 (8) ◽  
pp. 1257-1268 ◽  
Author(s):  
Andrei V. Malkov ◽  
Pavel Kočovský

∆9-Tetrahydrocannabinol 1 and its isomers were synthesized via domino-type methodology. The first approach, leading to (±)-1, relies on the Mo(IV)-catalyzed, one-pot cascade reaction of citral (4) with olivetol (15), affording (±)-∆9-tetrahydrocannabinol as a 69 : 31 mixture of the trans- (natural) and cis-isomers in 20% yield. The alternative approach, leading to natural (-)-1, commenced with epoxidation of (+)-limonene (R)-(+)-16; opening of the resulting cis-epoxide 17 with PhSeNa, followed by elimination, afforded tertiary alcohol 21, whose acetate 22 was treated with olivetol 15 in the presence of Mo(II) catalyst IV to afford (-)-1 in 52% yield.


2016 ◽  
Vol 6 (21) ◽  
pp. 7729-7737 ◽  
Author(s):  
Elena Rosini ◽  
Paola D'Arrigo ◽  
Loredano Pollegioni

Recombinant LigM from Sphingobium SYK-6 and plant methionine synthase MetE enzyme efficiently convert vanillic acid into PCA with cofactor recycling.


2020 ◽  
Vol 11 (42) ◽  
pp. 11455-11460 ◽  
Author(s):  
Archie Wall ◽  
Alfie G. Wills ◽  
Nafsika Forte ◽  
Calise Bahou ◽  
Lisa Bonin ◽  
...  
Keyword(s):  
One Pot ◽  

An alternative approach to maleimide conjugate stabilisation is presented, by the consecutive addition of a thiol and an amine to dibromomaleimides. The amine serves to simultaneously deactivate the maleimide and enable dual functionalisation.


ChemInform ◽  
2012 ◽  
Vol 43 (7) ◽  
pp. no-no
Author(s):  
Yi Chen ◽  
Vireak Thon ◽  
Yanhong Li ◽  
Hai Yu ◽  
Li Ding ◽  
...  
Keyword(s):  

2011 ◽  
Vol 47 (38) ◽  
pp. 10815 ◽  
Author(s):  
Yi Chen ◽  
Vireak Thon ◽  
Yanhong Li ◽  
Hai Yu ◽  
Li Ding ◽  
...  
Keyword(s):  

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