Penttilä M E, André L, Saloheimo M, Lehtovaara P, Knowles J K
VTT, Biotechnical Laboratory, Espoo, Finland.
Yeast. 1987 Sep;3(3):175-85. doi: 10.1002/yea.320030305.
The cDNA copies of the two endo-beta-1,4-glucanase genes, egl1 and egl3, from the filamentous fungus Trichoderma reesei were expressed in yeast Saccharomyces cerevisiae under the control of the yeast phosphoglycerate kinase gene promoter. Active EGI and EGIII enzyme was produced and secreted by yeast into the growth medium. The recombinant EGI enzyme was larger and more heterogeneous in size than the native enzyme secreted by Trichoderma, due to differences in the extent of N-glycosylation between these two organisms. The morphology of the yeast cells producing EGI or EGIII was clearly different from control strain.
来自丝状真菌里氏木霉的两个内切β-1,4-葡聚糖酶基因egl1和egl3的cDNA拷贝在酵母磷酸甘油酸激酶基因启动子的控制下在酿酒酵母中表达。酵母产生并分泌活性EGI和EGIII酶到生长培养基中。由于这两种生物体在N-糖基化程度上存在差异,重组EGI酶在大小上比里氏木霉分泌的天然酶更大且更具异质性。产生EGI或EGIII的酵母细胞形态与对照菌株明显不同。