Advances in biological conversion technologies: new opportunities for reaction engineering
Literature Information
Publication Date
2020-02-24
DOI
10.1039/C9RE00422J
Impact Factor
4.239
Authors
View Original
Abstract
Reaction engineering needs to embrace biological conversion technologies, on the road to identify more sustainable routes for chemical manufacture. There are new options in biological conversion including modifying the properties of an enzyme by protein engineering, a pathway by metabolic engineering or a microbial host cell. However, here also lies the challenge of a multitude of technologies and modes of operation, which the reaction engineer must navigate successfully in order to implement a new process. This perspective summarizes some of the recent developments in the field and the implications for reaction engineering, with a focus on sustainable chemical production.
Related Literature
Unraveling the binding interaction and kinetics of a prospective anti-HIV drug with a model transport protein: results and challenges
Bijan Kumar Paul, Debarati Ray, Nikhil Guchhait
2012-11-21
Paper
DOI: 10.1039/C2CP42539D
Microlens array induced light absorption enhancement in polymer solar cells
Yuqing Chen, Max A. Noack
2013-01-24
Paper
DOI: 10.1039/C3CP50297J
Interactions in different domains of truxenone supramolecular assembly on Au(111)
Fengyun Chen, Zhenpeng Hu, Yongfei Ji, Aidi Zhao, Bing Wang, Jinlong Yang, J. G. Hou
2012-01-23
Paper
DOI: 10.1039/C2CP23190E
A RASSCF study of free base, magnesium and zinc porphyrins: accuracy versus efficiency‡
Andrew Kerridge
2012-12-18
Paper
DOI: 10.1039/C2CP43982D
Polyallylamine-directed green synthesis of platinum nanocubes. Shape and electronic effect codependent enhanced electrocatalytic activity
Gengtao Fu, Ke Wu, Xian Jiang, Lin Tao, Yu Chen, Jun Lin, Yiming Zhou, Shaohua Wei, Yawen Tang, Tianhong Lu, Xinghua Xia
2013-01-10
Paper
DOI: 10.1039/C3CP44191A
The importance of the TiO2/quantum dots interface in the recombination processes of quantum dot sensitized solar cells
Zion Tachan, Idan Hod, Menny Shalom, Larissa Grinis, Arie Zaban
2013-01-23
Paper
DOI: 10.1039/C3CP44719G
Can hydrate form in carbon dioxide from dissolved water?
Bjørn Kvamme, Tatiana Kuznetsova, Pilvi-Helina Kivelæ, Jordan Bauman
2012-11-28
Paper
DOI: 10.1039/C2CP43061D
Ruthenium sulphide thin layers as catalysts for the electrooxidation of water
Peter Bogdanoff, Carolin Zachäus, Stephan Brunken, Andreas Kratzig, Klaus Ellmer, Sebastian Fiechter
2012-11-29
Paper
DOI: 10.1039/C2CP42348K
Enhanced electronic contacts in SnO2–dye–P3HT based solid state dye sensitized solar cells
Golnaz Sadoughi, Varun Sivaram, Robbert Gunning, Pablo Docampo, Ingmar Bruder, Neil Pschirer, Azam Irajizad, Henry J. Snaith
2013-01-03
Paper
DOI: 10.1039/C2CP43434B
You might also like
Compound Q&A
What is 3-Fluoro-2-methylbenzylamine (CAS: 771573-36-5)?
3-Fluoro-2-methylbenzylamine is an organic compound with the CAS number 771573-3...
771573-36-53-Fluoro-2-methylben...
Compound Q&A
Is Tert-butyl 2-(oxetan-3-ylidene)acetate (CAS: 1207175-03-8) safe?
Tert-butyl 2-(oxetan-3-ylidene)acetate is considered safe for its intended uses ...
1207175-03-8Tert-butyl 2-(oxetan...
Compound Q&A
What precautions should be taken when handling 4-Acetyl-2-fluorobenzonitrile (CAS: 214760-18-6)?
Proper personal protective equipment (PPE) such as gloves, goggles, and a lab co...
214760-18-64-Acetyl-2-fluoroben...
Compound Q&A
How is 2-Ethyl-4-methyl-1,3-thiazole (CAS: 15679-12-6) typically synthesized?
2-Ethyl-4-methyl-1,3-thiazole is commonly synthesized via the reaction of thiour...
15679-12-62-Ethyl-4-methyl-1,3...
Compound Q&A
How should 5',5''-([2,2'-Bithiophene]-5,5'-diyl)bis(([1,1':3',1''-terphenyl]-4,4''-dicarboxylic acid)) (CAS: 1227780-71-3) be stored?
This compound should be stored in a cool, dry place away from direct sunlight an...
1227780-71-35',5''''-([2,2'-Bith...
Compound Q&A
What regulatory guidelines apply to L-Lysine Acetate Salt (CAS: 52315-92-1)?
L-Lysine Acetate Salt (CAS: 52315-92-1) is subject to various regulatory guideli...
52315-92-1L-LYSINE ACETATE SAL...
Compound Q&A
Is 6-Fluoro-3-hydroxy-2-pyrazinecarboxamide (CAS: 259793-96-9) safe?
6-Fluoro-3-hydroxy-2-pyrazinecarboxamide (CAS: 259793-96-9) is generally conside...
259793-96-96-Fluoro-3-hydroxy-2...
Compound Q&A
What are the physical and chemical properties of 1,1'-Sulfonylbis(1H-imidazole) (CAS: 7189-69-7)?
1,1'-Sulfonylbis(1H-imidazole) is a crystalline solid with a molecular weight of...
7189-69-71,1'-Sulfonylbis(1H-...
Compound Q&A
What industries use 4-methyl-7-nitro-1H-indole-3-carbonitrile (CAS: 289483-82-5)?
4-Methyl-7-nitro-1H-indole-3-carbonitrile (CAS: 289483-82-5) is primarily used i...
289483-82-54-methyl-7-nitro-1H-...
Compound Q&A
How should waste containing 5-Bromo-3-indolyl-beta-galactoside (CAS: 97753-82-7) be handled?
Waste containing 5-Bromo-3-indolyl-beta-galactoside (CAS: 97753-82-7) should be ...
97753-82-75-Bromo-3-indolyl-be...
Source Journal
Reaction Chemistry & Engineering
CiteScore:
0
Self-citation Rate:
8.8%
Articles per Year:
284
Reaction Chemistry & Engineering is an interdisciplinary journal reporting cutting-edge research focused on enhancing the understanding and efficiency of reactions. Reaction engineering leverages the interface where fundamental molecular chemistry meets chemical engineering and technology. Challenges in chemistry can be overcome by the application of new technologies, while engineers may find improved solutions for process development from the latest developments in reaction chemistry. Reaction Chemistry & Engineering is a unique forum for researchers whose interests span the broad areas of chemical engineering and chemical sciences to come together in solving problems of importance to wider society. All papers should be written to be approachable by readers across the engineering and chemical sciences. Papers that consider multiple scales, from the laboratory up to and including plant scale, are particularly encouraged.
Recommended Compounds
![(1S,4aR,5R,7S,7aS)-1-(beta-D-Glucopyranosyloxy)-5-hydroxy-7-methyl-1,4a,5,6,7,7a-hexahydrocyclopenta[c]pyran-7-yl alpha-D-galactopyranoside structure](https://static.chemtradehub.com/structs/817/81720-07-2-4ffd.webp "(1S,4aR,5R,7S,7aS)-1-(beta-D-Glucopyranosyloxy)-5-hydroxy-7-methyl-1,4a,5,6,7,7a-hexahydrocyclopenta[c]pyran-7-yl alpha-D-galactopyranoside structure")
(1S,4aR,5R,7S,7aS)-1-(beta-D-Glucopyranosyloxy)-5-hydroxy-7-methyl-1,4a,5,6,7,7a-hexahydrocyclopenta[c]pyran-7-yl alpha-D-galactopyranoside
CAS Number:
81720-07-2
Molecular Formula:
C21H34O14
![5-(2-Phenylpyrazolo[1,5-a]pyridin-3-yl)-2H-pyrazolo[3,4-c]pyridazin-3-amine structure](https://static.chemtradehub.com/structs/865/865362-74-9-0091.webp "5-(2-Phenylpyrazolo[1,5-a]pyridin-3-yl)-2H-pyrazolo[3,4-c]pyridazin-3-amine structure")
5-(2-Phenylpyrazolo[1,5-a]pyridin-3-yl)-2H-pyrazolo[3,4-c]pyridazin-3-amine
CAS Number:
865362-74-9
Molecular Formula:
C18H13N7
Recommended Suppliers
Disclaimer
This page provides academic journal information for reference and research purposes only. We are not affiliated with any journal publishers and do not handle publication submissions. For publication-related inquiries, please contact the respective journal publishers directly.
If you notice any inaccuracies in the information displayed, please contact us at support@chemtradehub.com. We will promptly review and address your concerns.