Stacey G
Department of Microbiology, University of Tennessee, Knoxville 37996-0845.
FEMS Microbiol Lett. 1995 Mar 15;127(1-2):1-9. doi: 10.1111/j.1574-6968.1995.tb07441.x.
Studies of the genetics of nodulation by Bradyrhizobium japonicum have revealed many similar features with Rhizobium and Azorhizobium species, but also apparent differences. The regulation of nod gene expression in B. japonicum is complex, involving the interplay of the positive regulator, NodD1, as well as a repressor, No1A. A unique feature of B. japonicum is the involvement of a two-component regulatory system, NodV and NodW, in the control of nod gene expression. It is not clear why B. japonicum requires this level of complexity to control nod gene transcription. The nod gene products encode the biosynthesis of substituted lipo-chitin Nod signals that induce many of the early nodulation events. B. japonicum and B. elkanii produce a large variety of such Nod signals. The basic structure of the Nod signal, an acylated oligomer of N-acetylglucosamine, is synthesized through the action of NodA, NodB, and NodC. Various substitutions of this basic structure confer host specificity to the molecule. For example, in B. japonicum, the nodZ gene product is essential for fucosylation of the terminal, reducing N-acetylglucosamine residue. These observations argue for the interaction of a substituted Nod signal with a specific plant receptor molecule. However, structure/function studies using chemically synthesized Nod signal molecules suggest a more complex interaction between chain length and specific substitution. These findings leave open the possibility that a general chitin receptor may function in a unique way to elicit nodule formation. The novel features discovered through the study of B. japonicum contribute to our general understanding of nodulation and to the larger question of plant cell signal transduction.
对日本慢生根瘤菌结瘤遗传学的研究揭示了其与根瘤菌属和固氮根瘤菌属物种的许多相似特征,但也存在明显差异。日本慢生根瘤菌中结瘤基因表达的调控很复杂,涉及正调控因子NodD1以及阻遏因子No1A的相互作用。日本慢生根瘤菌的一个独特特征是双组分调控系统NodV和NodW参与了结瘤基因表达的控制。目前尚不清楚为什么日本慢生根瘤菌需要这种复杂程度来控制结瘤基因转录。结瘤基因产物编码诱导许多早期结瘤事件的取代脂壳寡糖结瘤信号的生物合成。日本慢生根瘤菌和埃氏慢生根瘤菌产生多种此类结瘤信号。结瘤信号的基本结构,即N-乙酰葡糖胺的酰化寡聚物,是通过NodA、NodB和NodC的作用合成的。这种基本结构的各种取代赋予了该分子宿主特异性。例如,在日本慢生根瘤菌中,nodZ基因产物对于末端还原性N-乙酰葡糖胺残基的岩藻糖基化至关重要。这些观察结果支持了取代的结瘤信号与特定植物受体分子相互作用的观点。然而,使用化学合成的结瘤信号分子进行的结构/功能研究表明,链长和特定取代之间存在更复杂的相互作用。这些发现留下了一种可能性,即一种通用的几丁质受体可能以独特的方式发挥作用以引发根瘤形成。通过对日本慢生根瘤菌的研究发现的新特征有助于我们对结瘤的总体理解以及植物细胞信号转导这一更大的问题。