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   https://doi.org/10.1128/aem.00445-25  

   Gallagher, Brian M; Morrison, Hailee M; Bose, Arpita (August 2025, Applied and Environmental Microbiology)

   Reguera, Gemma (Ed.)

   ABSTRACT Rhodopseudomonas palustrisis renowned for its metabolic versatility, supported by a genome that contains pathways for numerous processes. In a recent study, Oda et al. (Appl Environ Microbiol 91:e02056-24, 2025,https://doi.org/10.1128/aem.02056-24) examineR. palustrisDSM127, a strain with a dramatically reduced gene inventory, to study how environmental pressures have influenced gene loss. Missing more than a quarter of its genome reduces its versatility. However, it may improve its efficiency under the conditions in which it still thrives, enhancing its aptitude as a chassis for biotechnology. 

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2. Construction of vicinal 4°/3°-carbons via reductive Cope rearrangement

   https://doi.org/10.1039/d1sc06307c  

   Sobie, Kristin M.; Albritton, Matthew; Yang, Yinuo; Alves, Mariana M.; Roitberg, Adrian; Grenning, Alexander J. (February 2022, Chemical Science)

   Herein reported is a strategy for constructing vicinal 4°/3° carbons via reductive Cope rearrangement. Substrates have been designed which exhibit Cope rearrangement kinetic barriers of ∼23 kcal mol −1 with isoenergetic favorability (Δ G ∼ 0). These fluxional/shape-shifting molecules can be driven forward by chemoselective reduction to useful polyfunctionalized building blocks. 

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3. Impact of Fixed Nitrogen Availability on Dehalococcoides mccartyi Reductive Dechlorination Activity

   https://doi.org/10.1021/acs.est.9b04463  

   Kaya, Devrim; Kjellerup, Birthe V.; Chourey, Karuna; Hettich, Robert L.; Taggart, Dora M.; Löffler, Frank E. (November 2019, Environmental Science & Technology)
4. Ni-catalyzed two-component reductive dicarbofunctionalization of alkenes via radical cyclization

   https://doi.org/10.1039/c8cc00358k  

   Kuang, Yulong; Wang, Xuefeng; Anthony, David; Diao, Tianning (January 2018, Chemical Communications)

   A reductive dicarbofunctionalization reaction of alkenes has been developed and applied to the preparation of substituted carbo- and heterocycles. The reaction conditions avoid the use of air-sensitive organometallic reagents, and are compatible with a broad range of bromo-electrophiles and a wide variety of substituents to give cyclic products in excellent yields. 

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5. Respiratory Vinyl Chloride Reductive Dechlorination to Ethene in TceA-Expressing Dehalococcoides mccartyi

   https://doi.org/10.1021/acs.est.0c07354  

   Yan, Jun; Wang, Jingjing; Villalobos Solis, Manuel I.; Jin, Huijuan; Chourey, Karuna; Li, Xiuying; Yang, Yi; Yin, Yongchao; Hettich, Robert L.; Löffler, Frank E. (April 2021, Environmental Science & Technology)

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