Recent Development of Aerobic Oxidative Transformations by Flavin Catalysis

2022 ◽  
Vol 80 (1) ◽  
pp. 27-35
Author(s):  
Hiroki Iida
2014 ◽  
Vol 80 (10) ◽  
pp. 3044-3052 ◽  
Author(s):  
Alexey Vorobev ◽  
Sheeja Jagadevan ◽  
Sunit Jain ◽  
Karthik Anantharaman ◽  
Gregory J. Dick ◽  
...  

ABSTRACTA minority of methanotrophs are able to utilize multicarbon compounds as growth substrates in addition to methane. The pathways utilized by these microorganisms for assimilation of multicarbon compounds, however, have not been explicitly examined. Here, we report the draft genome of the facultative methanotrophMethylocystissp. strain SB2 and perform a detailed transcriptomic analysis of cultures grown with either methane or ethanol. Evidence for use of the canonical methane oxidation pathway and the serine cycle for carbon assimilation from methane was obtained, as well as for operation of the complete tricarboxylic acid (TCA) cycle and the ethylmalonyl-coenzyme A (EMC) pathway. Experiments withMethylocystissp. strain SB2 grown on methane revealed that genes responsible for the first step of methane oxidation, the conversion of methane to methanol, were expressed at a significantly higher level than those for downstream oxidative transformations, suggesting that this step may be rate limiting for growth of this strain with methane. Further, transcriptomic analyses ofMethylocystissp. strain SB2 grown with ethanol compared to methane revealed that on ethanol (i) expression of the pathway of methane oxidation and the serine cycle was significantly reduced, (ii) expression of the TCA cycle dramatically increased, and (iii) expression of the EMC pathway was similar. Based on these data, it appears thatMethylocystissp. strain SB2 converts ethanol to acetyl-coenzyme A, which is then funneled into the TCA cycle for energy generation or incorporated into biomass via the EMC pathway. This suggests that some methanotrophs have greater metabolic flexibility than previously thought and that operation of multiple pathways in these microorganisms is highly controlled and integrated.


1994 ◽  
Vol 35 (33) ◽  
pp. 6001-6004 ◽  
Author(s):  
Charles S. Swindell ◽  
Madhavi C. Chander

1999 ◽  
Vol 18 (4-5) ◽  
pp. 991-992
Author(s):  
Annika Kers ◽  
Inger Kers ◽  
Jacek Cieslak ◽  
Adam Kraszewski ◽  
Jacek Stawinski

ChemInform ◽  
2010 ◽  
Vol 30 (40) ◽  
pp. no-no
Author(s):  
V. P. Kazakov ◽  
A. I. Voloshin ◽  
D. V. Kazakov

2005 ◽  
Vol 77 (9) ◽  
pp. 1539-1557 ◽  
Author(s):  
Toshikazu Hirao

Oxovanadium(V) compounds serve as Lewis acids with oxidation capability and induce one-electron oxidative transformations of organosilicons, organotins, organoaluminums, organoborons, organozincs, and/or their ate complexes. Low-valent vanadium-catalyzed stereoselective reductive transformations, including dehalogenation, pinacol coupling, and the related radical reaction, have been developed by constructing a multicomponent redox system in combination with a coreductant and an additive.


Synlett ◽  
2020 ◽  
Author(s):  
Hai-Chao Xu ◽  
Fan Xu ◽  
Xiao-Li Lai

AbstractAn oxidant- and metal-free photoelectrocatalytic C–H alkylation reaction of heteroarenes with alkyl oxalates has been developed. Several classes of heteroaromatics, such as quinolines, isoquinolines, pyridines, and phenanthridines, can be alkylated with tertiary or secondary alkyl oxalates. The photoelectrochemical synthesis employs 2,4,5,6-tetra-9H-carbazol-9-ylisophthalonitrile as a molecular catalyst and allows the oxidative transformations to proceed through evolution of hydrogen without a sacrificial chemical oxidant.


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