Jiangsu Key Laboratory for Microbes and Microbial Functional Genomics, Jiangsu Engineering and Technology Research Center for Industrialization of Microbial Resources, College of Life Science, Nanjing Normal University, 1 Wenyuan Rd, Xianlin University Park, Nanjing 210046, PR China.
Jiangsu Key Laboratory for Microbes and Microbial Functional Genomics, Jiangsu Engineering and Technology Research Center for Industrialization of Microbial Resources, College of Life Science, Nanjing Normal University, 1 Wenyuan Rd, Xianlin University Park, Nanjing 210046, PR China.
Int J Biol Macromol. 2020 Jun 1;152:516-524. doi: 10.1016/j.ijbiomac.2020.02.299. Epub 2020 Feb 26.
We previously reported endo-β-1,3-glucanase ENG in combination with β-glucosidase BGL2 at low concentration induced stipe cell wall extension. This study further explored ENG could be replaced by endo-β-1,3(4)-glucanase ENG16A in combination with BGL2 to induce stipe cell wall extension; similarly, BGL2 could be replaced by β-glucosidase BGL1 to cooperate with ENG to induce stipe cell wall extension. However, ENG could not be replaced by exo-β-1,3-glucanase EXG in combination with BGL2 to induce stipe cell wall extension, although EXG alone released higher level of soluble sugars from the stipe cell walls during the reconstituted wall extension than that released from the stipe cell walls by a combination of ENG16A or ENG and BGL2 or BGL1, which was different from chitinase-mediated stipe cell wall extension. These results indicate endo-β-1,3-glucanases loosen the stipe cell wall, whereas exo-β-1,3-glucanases and β-glucosidases play a synergistic role to maintain a low and efficient concentration of endo-β-1,3-glucanases for stipe cell wall extension. Furthermore, ENG was expressed at a very high level in the matured pilei, in contrast, ENG16A was expressed at a very high level in the elongating apical stipe. Therefore, ENG16A might be involved in stipe elongation growth, while ENG might participate in autolysis of pilei.
我们之前报道过,低浓度的内切-β-1,3-葡聚糖酶 ENG 与β-葡萄糖苷酶 BGL2 联合作用会诱导菌柄细胞壁延伸。本研究进一步探索了 ENG 能否被内切-β-1,3(4)-葡聚糖酶 ENG16A 替代,与 BGL2 联合诱导菌柄细胞壁延伸;同样,BGL2 也可以被β-葡萄糖苷酶 BGL1 替代,与 ENG 协同作用诱导菌柄细胞壁延伸。然而,尽管 EXG 单独作用于重组细胞壁延伸时,从菌柄细胞壁中释放的可溶性糖水平高于 ENG16A 或 ENG 与 BGL2 或 BGL1 联合作用时,但 EXG 不能替代内切-β-1,3-葡聚糖酶 ENG 与 BGL2 联合作用诱导菌柄细胞壁延伸。这与几丁质酶介导的菌柄细胞壁延伸不同。这些结果表明,内切-β-1,3-葡聚糖酶疏松菌柄细胞壁,而外切-β-1,3-葡聚糖酶和β-葡萄糖苷酶协同作用,维持低而高效的内切-β-1,3-葡聚糖酶浓度,以促进菌柄细胞壁延伸。此外,ENG 在成熟的菌盖上表达水平非常高,而 ENG16A 在伸长的菌柄顶端表达水平非常高。因此,ENG16A 可能参与菌柄伸长生长,而 ENG 可能参与菌盖的自溶。