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- W3136264124 endingPage "112668" @default.
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- W3136264124 abstract "We review glucosinolate (GSL) diversity and analyze phylogeny in the crucifer tribe Cardamineae as well as selected species from Brassicaceae (tribe Brassiceae) and Resedaceae. Some GSLs occur widely, while there is a scattered distribution of many less common GSLs, tentatively sorted into three classes: ancient, intermediate and more recently evolved. The number of conclusively identified GSLs in the tribe (53 GSLs) constitute 60% of all GSLs known with certainty from any plant (89 GSLs) and apparently unique GSLs in the tribe constitute 10 of those GSLs conclusively identified (19%). Intraspecific, qualitative GSL polymorphism is known from at least four species in the tribe. The most ancient GSL biosynthesis in Brassicales probably involved biosynthesis from Phe, Val, Leu, Ile and possibly Trp, and hydroxylation at the β-position. From a broad comparison of families in Brassicales and tribes in Brassicaceae, we estimate that a common ancestor of the tribe Cardamineae and the family Brassicaceae exhibited GSL biosynthesis from Phe, Val, Ile, Leu, possibly Tyr, Trp and homoPhe (ancient GSLs), as well as homologs of Met and possibly homoIle (intermediate age GSLs). From the comparison of phylogeny and GSL diversity, we also suggest that hydroxylation and subsequent methylation of indole GSLs and usual modifications of Met-derived GSLs (formation of sulfinyls, sulfonyls and alkenyls) occur due to conserved biochemical mechanisms and was present in a common ancestor of the family. Apparent loss of homologs of Met as biosynthetic precursors was deduced in the entire genus Barbarea and was frequent in Cardamine (e.g. C. pratensis, C. diphylla, C. concatenata, possibly C. amara). The loss was often associated with appearance of significant levels of unique or rare GSLs as well as recapitulation of ancient types of GSLs. Biosynthetic traits interpreted as de novo evolution included hydroxylation at rare positions, acylation at the thioglucose and use of dihomoIle and possibly homoIle as biosynthetic precursors. Biochemical aspects of the deduced evolution are discussed and testable hypotheses proposed. Biosyntheses from Val, Leu, Ile, Phe, Trp, homoPhe and homologs of Met are increasingly well understood, while GSL biosynthesis from mono- and dihomoIle is poorly understood. Overall, interpretation of known diversity suggests that evolution of GSL biosynthesis often seems to recapitulate ancient biosynthesis. In contrast, unprecedented GSL biosynthetic innovation seems to be rare." @default.
- W3136264124 created "2021-03-29" @default.
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- W3136264124 date "2021-05-01" @default.
- W3136264124 modified "2023-09-29" @default.
- W3136264124 title "Comparison of glucosinolate diversity in the crucifer tribe Cardamineae and the remaining order Brassicales highlights repetitive evolutionary loss and gain of biosynthetic steps" @default.
- W3136264124 cites W1563360496 @default.
- W3136264124 cites W1854649813 @default.
- W3136264124 cites W1875727809 @default.
- W3136264124 cites W1895822307 @default.
- W3136264124 cites W1966841179 @default.
- W3136264124 cites W1968924368 @default.
- W3136264124 cites W1973007396 @default.
- W3136264124 cites W1975916027 @default.
- W3136264124 cites W1976375318 @default.
- W3136264124 cites W1977650606 @default.
- W3136264124 cites W1979929176 @default.
- W3136264124 cites W1980614332 @default.
- W3136264124 cites W1980976814 @default.
- W3136264124 cites W1984149259 @default.
- W3136264124 cites W1985362460 @default.
- W3136264124 cites W1990240355 @default.
- W3136264124 cites W1992605508 @default.
- W3136264124 cites W1994375963 @default.
- W3136264124 cites W1996005833 @default.
- W3136264124 cites W1997628735 @default.
- W3136264124 cites W2001807768 @default.
- W3136264124 cites W2015305370 @default.
- W3136264124 cites W2024012002 @default.
- W3136264124 cites W2027708707 @default.
- W3136264124 cites W2028163231 @default.
- W3136264124 cites W2030099286 @default.
- W3136264124 cites W2033829351 @default.
- W3136264124 cites W2038950613 @default.
- W3136264124 cites W2048183777 @default.
- W3136264124 cites W2053302900 @default.
- W3136264124 cites W2056991865 @default.
- W3136264124 cites W2057628981 @default.
- W3136264124 cites W2058554887 @default.
- W3136264124 cites W2065735257 @default.
- W3136264124 cites W2068329415 @default.
- W3136264124 cites W2069226672 @default.
- W3136264124 cites W2070903997 @default.
- W3136264124 cites W2071342447 @default.
- W3136264124 cites W2071903673 @default.
- W3136264124 cites W2073846298 @default.
- W3136264124 cites W2074059297 @default.
- W3136264124 cites W2076589187 @default.
- W3136264124 cites W2077458840 @default.
- W3136264124 cites W2078501360 @default.
- W3136264124 cites W2086430107 @default.
- W3136264124 cites W2086545969 @default.
- W3136264124 cites W2091222115 @default.
- W3136264124 cites W2092219373 @default.
- W3136264124 cites W2092457863 @default.
- W3136264124 cites W2092850770 @default.
- W3136264124 cites W2099299146 @default.
- W3136264124 cites W2102005894 @default.
- W3136264124 cites W2103196745 @default.
- W3136264124 cites W2106967192 @default.
- W3136264124 cites W2113571125 @default.
- W3136264124 cites W2117805596 @default.
- W3136264124 cites W2117859069 @default.
- W3136264124 cites W2119428511 @default.
- W3136264124 cites W2121233554 @default.
- W3136264124 cites W2133174791 @default.
- W3136264124 cites W2137532647 @default.
- W3136264124 cites W2140192834 @default.
- W3136264124 cites W2146058063 @default.
- W3136264124 cites W2157314891 @default.
- W3136264124 cites W2157843402 @default.
- W3136264124 cites W2161444534 @default.
- W3136264124 cites W2162657654 @default.
- W3136264124 cites W2167089428 @default.
- W3136264124 cites W2168920064 @default.
- W3136264124 cites W2201030323 @default.
- W3136264124 cites W2226686169 @default.
- W3136264124 cites W2266854835 @default.
- W3136264124 cites W2313524423 @default.
- W3136264124 cites W2322442544 @default.
- W3136264124 cites W2328092798 @default.
- W3136264124 cites W2332465169 @default.
- W3136264124 cites W2332477179 @default.
- W3136264124 cites W2363140615 @default.
- W3136264124 cites W2400074828 @default.
- W3136264124 cites W2415473721 @default.
- W3136264124 cites W2421979005 @default.
- W3136264124 cites W2442262621 @default.
- W3136264124 cites W2461836122 @default.
- W3136264124 cites W2486347113 @default.
- W3136264124 cites W2498192911 @default.