Advanced Search
Display options
Filter resources
Text Availability
Article type
Publication date
Species
Language
Sex
Age
Showing 1 to 2 of 2 entries
Sorted by: Best Match Show Resources per page
Engineering Escherichia coli for anaerobic alkane activation: Biosynthesis of (1-methylalkyl)succinates.

Biotechnology and bioengineering

Wang Y, Nguyen N, Lee SH, Wang Q, May JA, Gonzalez R, Cirino PC.
PMID: 34633065
Biotechnol Bioeng. 2022 Jan;119(1):315-320. doi: 10.1002/bit.27956. Epub 2021 Oct 16.

In anoxic environments, microbial activation of alkanes for subsequent metabolism occurs most commonly through the addition of fumarate to a subterminal carbon, producing an alkylsuccinate. Alkylsuccinate synthases are complex, multi-subunit enzymes that utilize a catalytic glycyl radical and require...

Cite
Wang Y, Nguyen N, Lee SH, et al. Engineering Escherichia coli for anaerobic alkane activation: Biosynthesis of (1-methylalkyl)succinates. Biotechnol Bioeng. 2021;119(1):315-320doi: 10.1002/bit.27956.
Wang, Y., Nguyen, N., Lee, S. H., Wang, Q., May, J. A., Gonzalez, R., & Cirino, P. C. (2022). Engineering Escherichia coli for anaerobic alkane activation: Biosynthesis of (1-methylalkyl)succinates. Biotechnology and bioengineering, 119(1), 315-320. https://doi.org/10.1002/bit.27956
Wang, Yixi, et al. "Engineering Escherichia coli for anaerobic alkane activation: Biosynthesis of (1-methylalkyl)succinates." Biotechnology and bioengineering vol. 119,1 (2022): 315-320. doi: https://doi.org/10.1002/bit.27956
Wang Y, Nguyen N, Lee SH, Wang Q, May JA, Gonzalez R, Cirino PC. Engineering Escherichia coli for anaerobic alkane activation: Biosynthesis of (1-methylalkyl)succinates. Biotechnol Bioeng. 2022 Jan;119(1):315-320. doi: 10.1002/bit.27956. Epub 2021 Oct 16. PMID: 34633065.
Copy Download .nbib Format: NLM
Rate Dependence on Inductive and Resonance Effects for the Organocatalyzed Enantioselective Conjugate Addition of Alkenyl and Alkynyl Boronic Acids to β-Indolyl Enones and β-Pyrrolyl Enones.

Molecules (Basel, Switzerland)

Boylan A, Nguyen TS, Lundy BJ, Li JY, Vallakati R, Sundstrom S, May JA.
PMID: 33799473
Molecules. 2021 Mar 14;26(6). doi: 10.3390/molecules26061615.

Two key factors bear on reaction rates for the conjugate addition of alkenyl boronic acids to heteroaryl-appended enones: the proximity of inductively electron-withdrawing heteroatoms to the site of bond formation and the resonance contribution of available heteroatom lone pairs...

Cite
Boylan A, Nguyen TS, Lundy BJ, et al. Rate Dependence on Inductive and Resonance Effects for the Organocatalyzed Enantioselective Conjugate Addition of Alkenyl and Alkynyl Boronic Acids to β-Indolyl Enones and β-Pyrrolyl Enones. Molecules. 2021;26(6)doi: 10.3390/molecules26061615.
Boylan, A., Nguyen, T. S., Lundy, B. J., Li, J. Y., Vallakati, R., Sundstrom, S., & May, J. A. (2021). Rate Dependence on Inductive and Resonance Effects for the Organocatalyzed Enantioselective Conjugate Addition of Alkenyl and Alkynyl Boronic Acids to β-Indolyl Enones and β-Pyrrolyl Enones. Molecules (Basel, Switzerland), 26(6), . https://doi.org/10.3390/molecules26061615
Boylan, Amy, et al. "Rate Dependence on Inductive and Resonance Effects for the Organocatalyzed Enantioselective Conjugate Addition of Alkenyl and Alkynyl Boronic Acids to β-Indolyl Enones and β-Pyrrolyl Enones." Molecules (Basel, Switzerland) vol. 26,6 (2021). doi: https://doi.org/10.3390/molecules26061615
Boylan A, Nguyen TS, Lundy BJ, Li JY, Vallakati R, Sundstrom S, May JA. Rate Dependence on Inductive and Resonance Effects for the Organocatalyzed Enantioselective Conjugate Addition of Alkenyl and Alkynyl Boronic Acids to β-Indolyl Enones and β-Pyrrolyl Enones. Molecules. 2021 Mar 14;26(6). doi: 10.3390/molecules26061615. PMID: 33799473; PMCID: PMC8000498.
Copy Download .nbib Format: NLM
Showing 1 to 2 of 2 entries