Borjian Farshad, Johnsen Ulrike, Schönheit Peter, Berg Ivan A
Institut für Molekulare Mikrobiologie und Biotechnologie, Westfälische Wilhelms-Universität MünsterMünster, Germany.
Mikrobiologie, Fakultät für Biologie, Albert-Ludwigs-Universität FreiburgFreiburg, Germany.
Front Microbiol. 2017 Sep 6;8:1683. doi: 10.3389/fmicb.2017.01683. eCollection 2017.
Growth on acetate or other acetyl-CoA-generating substrates as a sole source of carbon requires an anaplerotic pathway for the conversion of acetyl-CoA into cellular building blocks. Haloarchaea (class ) possess two different anaplerotic pathways, the classical glyoxylate cycle and the novel methylaspartate cycle. The methylaspartate cycle was discovered in spp. and operates in ∼40% of sequenced haloarchaea. In this cycle, condensation of one molecule of acetyl-CoA with oxaloacetate gives rise to citrate, which is further converted to 2-oxoglutarate and then to glutamate. The following glutamate rearrangement and deamination lead to mesaconate (methylfumarate) that needs to be activated to mesaconyl-C1-CoA and hydrated to β-methylmalyl-CoA. The cleavage of β-methylmalyl-CoA results in the formation of propionyl-CoA and glyoxylate. The carboxylation of propionyl-CoA and the condensation of glyoxylate with another acetyl-CoA molecule give rise to two C-dicarboxylic acids, thus regenerating the initial acetyl-CoA acceptor and forming malate, its final product. Here we studied two enzymes of the methylaspartate cycle from , succinyl-CoA:mesaconate CoA-transferase (mesaconate CoA-transferase, Hah_1336) and mesaconyl-CoA hydratase (Hah_1340). Their genes were heterologously expressed in , and the corresponding enzymes were purified and characterized. Mesaconate CoA-transferase was specific for its physiological substrates, mesaconate and succinyl-CoA, and produced only mesaconyl-C1-CoA and no mesaconyl-C4-CoA. Mesaconyl-CoA hydratase had a 3.5-fold bias for the physiological substrate, mesaconyl-C1-CoA, compared to mesaconyl-C4-CoA, and virtually no activity with other tested enoyl-CoA/3-hydroxyacyl-CoA compounds. Our results further prove the functioning of the methylaspartate cycle in haloarchaea and suggest that mesaconate CoA-transferase and mesaconyl-CoA hydratase can be regarded as characteristic enzymes of this cycle.
以乙酸盐或其他生成乙酰辅酶A的底物作为唯一碳源进行生长,需要一条回补途径将乙酰辅酶A转化为细胞组成成分。嗜盐古菌(纲)拥有两条不同的回补途径,即经典的乙醛酸循环和新的甲基天冬氨酸循环。甲基天冬氨酸循环于种中被发现,约40%已测序的嗜盐古菌中存在该循环。在这个循环中,一分子乙酰辅酶A与草酰乙酸缩合生成柠檬酸,柠檬酸进一步转化为2-氧代戊二酸,然后转化为谷氨酸。随后的谷氨酸重排和脱氨生成中康酸(甲基富马酸),中康酸需要被激活为中康酰-C1-辅酶A并水合为β-甲基苹果酰辅酶A。β-甲基苹果酰辅酶A的裂解导致丙酰辅酶A和乙醛酸的形成。丙酰辅酶A的羧化以及乙醛酸与另一个乙酰辅酶A分子的缩合生成两个C-二羧酸,从而再生初始的乙酰辅酶A受体并形成其最终产物苹果酸。在此,我们研究了来自的甲基天冬氨酸循环的两种酶,琥珀酰辅酶A:中康酸辅酶A转移酶(中康酸辅酶A转移酶,Hah_1336)和中康酰辅酶A水合酶(Hah_1340)。它们的基因在中进行异源表达,相应的酶被纯化并进行了表征。中康酸辅酶A转移酶对其生理底物中康酸和琥珀酰辅酶A具有特异性,仅产生中康酰-C1-辅酶A,不产生中康酰-C4-辅酶A。与中康酰-C4-辅酶A相比,中康酰辅酶A水合酶对生理底物中康酰-C1-辅酶A的偏好性为3.5倍,并且对其他测试的烯酰辅酶A/3-羟基酰基辅酶A化合物几乎没有活性。我们的结果进一步证明了甲基天冬氨酸循环在嗜盐古菌中的功能,并表明中康酸辅酶A转移酶和中康酰辅酶A水合酶可被视为该循环的特征酶。