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Keywords: quinone
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Articles
Pu Qian, David J.K. Swainsbury, Tristan I. Croll, Jack H. Salisbury, Elizabeth C. Martin, Philip J. Jackson, Andrew Hitchcock, Pablo Castro-Hartmann, Kasim Sader, C. Neil Hunter
Journal:
Biochemical Journal
Biochem J (2021) 478 (20): 3775–3790.
Published: 21 October 2021
...-subunit LH1 ring in which each αβ heterodimer binds two bacteriochlorophylls and, unusually for currently reported complexes, two carotenoids rather than one. Although the extra carotenoids confer an advantage in terms of photoprotection and light harvesting, they could impede passage of quinones through...
Includes: Supplementary data
Articles
Pu Qian, Tristan I. Croll, David J.K. Swainsbury, Pablo Castro-Hartmann, Nigel W. Moriarty, Kasim Sader, C. Neil Hunter
Journal:
Biochemical Journal
Biochem J (2021) 478 (17): 3253–3263.
Published: 07 September 2021
... the RC, with a preferential binding site for a quinone, designated Q P , on the inner face of the encircling LH1 complex. Quinols, initially generated at the RC Q B site, are proposed to transiently occupy the Q P site prior to traversing the LH1 barrier and diffusing to the cytochrome bc 1 complex. Thus...
Includes: Supplementary data
Articles
Catalytic reaction of cytokinin dehydrogenase: preference for quinones as electron acceptors
Available to PurchaseJitka FRÉBORTOVÁ, Marco W. FRAAIJE, Petr GALUSZKA, Marek ŠEBELA, Pavel PEČ, Jan HRBÁČ, Ondřej NOVÁK, Kristin D. BILYEU, James T. ENGLISH, Ivo FRÉBORT
Journal:
Biochemical Journal
Biochem J (2004) 380 (1): 121–130.
Published: 15 May 2004
..., turnover rates with N 6 -(2-isopentenyl)adenine of approx. 150 s −1 could be obtained. This suggests that the natural electron acceptor of the enzyme is quite probably a p -quinone or similar compound. By using the stopped-flow technique, it was found that the enzyme is rapidly reduced by N 6 -(2...