Kubien David S, Whitney Spencer M, Moore Paige V, Jesson Linley K
Department of Biology, The University of New Brunswick, Box 4400, Fredericton, New Brunswick, E3B 5A3, Canada.
J Exp Bot. 2008;59(7):1767-77. doi: 10.1093/jxb/erm283. Epub 2008 Jan 27.
C(4) plants have been reported to have Rubiscos with higher maximum carboxylation rates (kcat(CO(2))) and Michaelis-Menten constants (K(m)) for CO(2) (K(c)) than the enzyme from C(3) species, but variation in other kinetic parameters between the two photosynthetic pathways has not been extensively examined. The CO(2)/O(2) specificity (S(C/O)), kcat(CO(2)), K(c), and the K(m) for O(2) (K(o)) and RuBP (K(m-RuBP)), were measured at 25 degrees C, in Rubisco purified from 16 species of Flaveria (Asteraceae). Our analysis included two C(3) species of Flaveria, four C(4) species, and ten C(3)-C(4) or C(4)-like species, in addition to other C(4) (Zea mays and Amaranthus edulis) and C(3) (Spinacea oleracea and Chenopodium album) plants. The S(C/O) of the C(4) Flaveria species was about 77 mol mol(-1), which was approximately 5% lower than the corresponding value in the C(3) species. For Rubisco from the C(4) Flaverias kcat(CO(2)) and K(c) were 23% and 45% higher, respectively, than for Rubisco from the C(3) plants. Interestingly, it was found that the K(o) for Rubisco from the C(4) species F. bidentis and F. trinervia were similar to the C(3) Flaveria Rubiscos (approximately 650 microM) while the K(o) for Rubisco in the C(4) species F. kochiana, F. australasica, Z. mays, and A. edulis was reduced more than 2-fold. There were no pathway-related differences in K(m-RuBP). In the C(3)-C(4) species kcat(CO(2)) and K(c) were generally similar to the C(3) Rubiscos, but the K(o) values were more variable. The typical negative relationships were observed between S(C/O) and both kcat(CO(2)) and K(c), and a strongly positive relationship was observed between kcat(CO(2)) and Kc. However, the statistical significance of these relationships was influenced by the phylogenetic relatedness of the species.
据报道,C(4)植物的核酮糖-1,5-二磷酸羧化酶/加氧酶(Rubisco)对CO(2)的最大羧化速率(kcat(CO(2)))和米氏常数(K(m))(即K(c))高于C(3)植物的该酶,但尚未广泛研究这两种光合途径之间其他动力学参数的差异。在25摄氏度下,测定了从16种黄顶菊属(菊科)植物中纯化得到的Rubisco的CO(2)/O(2)特异性(S(C/O))、kcat(CO(2))、K(c)以及对O(2)的K(m)(K(o))和对核酮糖-1,5-二磷酸(RuBP)的K(m)(K(m-RuBP))。我们的分析包括2种C(3)黄顶菊属植物、4种C(4)植物以及10种C(3)-C(4)或C(4)类植物,此外还有其他C(4)植物(玉米和可食苋)和C(3)植物(菠菜和藜)。C(4)黄顶菊属植物的S(C/O)约为77 μmol·mol⁻¹,比C(3)植物的相应值低约5%。对于C(4)黄顶菊属植物的Rubisco,kcat(CO(2))和K(c)分别比C(3)植物的Rubisco高23%和45%。有趣的是,发现C(4)植物二齿黄顶菊和三脉黄顶菊的Rubisco的K(o)与C(3)黄顶菊属植物的Rubisco相似(约650 μM),而C(4)植物科氏黄顶菊、澳洲黄顶菊、玉米和可食苋的Rubisco的K(o)降低了2倍以上。K(m-RuBP)没有与光合途径相关的差异。在C(3)-C(4)植物中,kcat(CO(2))和K(c)通常与C(3)植物的Rubisco相似,但K(o)值变化更大。在S(C/O)与kcat(CO(2))和K(c)之间观察到典型的负相关关系,在kcat(CO(2))与Kc之间观察到强正相关关系。然而,这些关系的统计学显著性受物种系统发育相关性的影响。