Rossbach S, Hennecke H
Mikrobiologisches Institut, Eidgenössische Technische Hochschule, ETH-Zentrum, Zürich, Switzerland.
Mol Microbiol. 1991 Jan;5(1):39-47. doi: 10.1111/j.1365-2958.1991.tb01824.x.
A Bradyrhizobium japonicum Tn5 mutant (strain 3160) induced numerous, tiny, white nodules which were dispersed over the whole root system of its natural host plant, soybean (Glycine max). These ineffective, nitrogen non-fixing pseudonodules were disturbed at a very early step of bacteroid and nodule development. Subsequent cloning and sequencing of the DNA region mutated in strain 3160 revealed that the Tn5 insertion mapped in a gene that had 60% homology to the Escherichia coli glyA gene coding for serine hydroxymethyltransferase (SHMT; E.C.2.1.2.1.). SHMT catalyses the biosynthesis of glycine from serine and the transfer of a one-carbon unit to tetrahydrofolate. The B. japonicum glyA region was able to fully complement the glycine auxotrophy of an E. coli glyA deletion strain. Although the Tn5 insertion in B. japonicum mutant 3160 disrupted the glyA coding sequence, this strain was only a bradytroph (i.e. a leaky auxotroph). Thus, B. japonicum may have an additional pathway for glycine biosynthesis. Nevertheless, the glyA mutation was responsible for the drastic symbiotic phenotype visible on plants. It may be possible, therefore, that a sufficient supply with glycine and/or a functioning C1-metabolism are indispensable for the establishment of a fully effective, nitrogen-fixing root nodule symbiosis.
慢生根瘤菌的一个Tn5突变体(菌株3160)在其天然宿主植物大豆(Glycine max)的整个根系上诱导形成了大量微小的白色根瘤。这些无效的、不固氮的假根瘤在类菌体和根瘤发育的早期阶段就受到了干扰。随后对菌株3160中发生突变的DNA区域进行克隆和测序,结果显示Tn5插入到了一个与大肠杆菌glyA基因具有60%同源性的基因中,该大肠杆菌glyA基因编码丝氨酸羟甲基转移酶(SHMT;E.C.2.1.2.1.)。SHMT催化由丝氨酸合成甘氨酸,并将一个一碳单位转移至四氢叶酸。慢生根瘤菌的glyA区域能够完全互补大肠杆菌glyA缺失菌株的甘氨酸营养缺陷型。尽管慢生根瘤菌突变体3160中的Tn5插入破坏了glyA编码序列,但该菌株只是一个生长缓慢的菌株(即渗漏营养缺陷型)。因此,慢生根瘤菌可能还有一条甘氨酸生物合成的额外途径。然而,glyA突变导致了在植物上可见的剧烈共生表型。因此,充足的甘氨酸供应和/或正常运作的一碳代谢对于建立完全有效的固氮根瘤共生关系可能是必不可少的。