Arrieta Juan G, Sotolongo Mailin, Menéndez Carmen, Alfonso Dubiel, Trujillo Luis E, Soto Melvis, Ramírez Ricardo, Hernández Lázaro
Plant-Microbe Interactions Lab, Plant Division, Center for Genetic Engineering and Biotechnology, P.O. Box 6162, Havana 10600, Cuba.
J Bacteriol. 2004 Aug;186(15):5031-9. doi: 10.1128/JB.186.15.5031-5039.2004.
The endophytic diazotroph Gluconacetobacter diazotrophicus secretes a constitutively expressed levansucrase (LsdA, EC 2.4.1.10) to utilize plant sucrose. LsdA, unlike other extracellular levansucrases from gram-negative bacteria, is transported to the periplasm by a signal-peptide-dependent pathway. We identified an unusually organized gene cluster encoding at least the components LsdG, -O, -E, -F, -H, -I, -J, -L, -M, -N, and -D of a type II secretory system required for LsdA translocation across the outer membrane. Another open reading frame, designated lsdX, is located between the operon promoter and lsdG, but it was not identified in BLASTX searches of the DDBJ/EMBL/GenBank databases. The lsdX, -G, and -O genes were isolated from a cosmid library of strain SRT4 by complementation of an ethyl methanesulfonate mutant unable to transport LsdA across the outer membrane. The downstream genes lsdE, -F, -H, -I, -J, -L, -M, -N, and -D were isolated through chromosomal walking. The high G+C content (64 to 74%) and the codon usage of the genes identified are consistent with the G+C content and codon usage of the standard G. diazotrophicus structural gene. Sequence analysis of the gene cluster indicated that a polycistronic transcript is synthesized. Targeted disruption of lsdG, lsdO, or lsdF blocked LsdA secretion, and the bacterium failed to grow on sucrose. Replacement of Cys(162) by Gly at the C terminus of the pseudopilin LsdG abolished the protein functionality, suggesting that there is a relationship with type IV pilins. Restriction fragment length polymorphism analysis revealed conservation of the type II secretion operon downstream of the levansucrase-levanase (lsdA-lsdB) locus in 14 G. diazotrophicus strains representing 11 genotypes recovered from four different host plants in diverse geographical regions. To our knowledge, this is the first report of a type II pathway for protein secretion in the Acetobacteraceae.
内生固氮菌重氮营养醋杆菌分泌一种组成型表达的果聚糖蔗糖酶(LsdA,EC 2.4.1.10)以利用植物蔗糖。与革兰氏阴性菌的其他胞外果聚糖蔗糖酶不同,LsdA通过依赖信号肽的途径转运至周质。我们鉴定出一个组织异常的基因簇,其编码LsdA跨外膜转运所需的II型分泌系统的至少LsdG、-O、-E、-F、-H、-I、-J、-L、-M、-N和-D组分。另一个开放阅读框,命名为lsdX,位于操纵子启动子和lsdG之间,但在DDBJ/EMBL/GenBank数据库的BLASTX搜索中未被鉴定出来。通过对一株无法将LsdA转运过外膜的甲磺酸乙酯突变体进行互补,从菌株SRT4的黏粒文库中分离出lsdX、-G和-O基因。通过染色体步移分离出下游基因lsdE、-F、-H、-I、-J、-L、-M、-N和-D。所鉴定基因的高G+C含量(64%至74%)和密码子使用情况与标准重氮营养醋杆菌结构基因的G+C含量和密码子使用情况一致。基因簇的序列分析表明合成了多顺反子转录本。对lsdG、lsdO或lsdF进行靶向破坏会阻断LsdA的分泌,并且该细菌无法在蔗糖上生长。在假菌毛蛋白LsdG的C末端将Cys(162)替换为Gly会消除蛋白质功能,这表明与IV型菌毛蛋白存在关联。限制性片段长度多态性分析显示,在从不同地理区域的四种不同宿主植物中分离出的代表11种基因型的14株重氮营养醋杆菌菌株中,果聚糖蔗糖酶-果聚糖酶(lsdA-lsdB)基因座下游的II型分泌操纵子具有保守性。据我们所知,这是醋杆菌科中蛋白质分泌II型途径的首次报道。