Shinabarger D, May T B, Boyd A, Ghosh M, Chakrabarty A M
Department of Microbiology and Immunology, University of Illinois College of Medicine, Chicago 60612.
Mol Microbiol. 1993 Sep;9(5):1027-35. doi: 10.1111/j.1365-2958.1993.tb01232.x.
Colonization of the cystic fibrosis lung by Pseudomonas aeruginosa is greatly facilitated by the production of an exopolysaccharide called alginate. In this study we determined the nucleotide sequence of an alginate modification gene, algF, which controls the addition of acetyl groups to alginate. Expression of algF using a T7 promoter-expression system showed that algF codes for a 24.5 kDa polypeptide (predicted size 22,832 Da) that is processed to 19.5 kDa. The N-terminus of the processed polypeptide matched the predicted amino acid sequence of AlgF starting at Asp-29. An algF mutant failed to produce alginate owing to a polar effect on the downstream algA gene. Although the algA gene, provided in trans, restored synthesis of alginate, the alginate was non-acetylated. We show that a plasmid containing both the algF and algA gene complements the alginate acetylation defect of the algF mutant strain.
铜绿假单胞菌产生一种名为藻酸盐的胞外多糖,这极大地促进了其在囊性纤维化肺中的定植。在本研究中,我们确定了一个藻酸盐修饰基因algF的核苷酸序列,该基因控制藻酸盐乙酰基的添加。使用T7启动子表达系统表达algF表明,algF编码一种24.5 kDa的多肽(预测大小为22,832 Da),该多肽经加工后变为19.5 kDa。加工后多肽的N端与从Asp-29开始的AlgF预测氨基酸序列匹配。由于对下游algA基因的极性效应,algF突变体无法产生藻酸盐。尽管反式提供的algA基因恢复了藻酸盐的合成,但藻酸盐未被乙酰化。我们表明,含有algF和algA基因的质粒可弥补algF突变菌株的藻酸盐乙酰化缺陷。