Reinhold-Hurek B, Hurek T, Claeyssens M, van Montagu M
Laboratorium voor Genetika, Universiteit Gent, Belgium.
J Bacteriol. 1993 Nov;175(21):7056-65. doi: 10.1128/jb.175.21.7056-7065.1993.
We screened members of a new genus of grass-associated diazotrophs (Azoarcus spp.) for the presence of cellulolytic enzymes. Out of five Azoarcus strains representing different species, only in the endorhizosphere isolate BH72, which is also capable of invading grass roots, was significant endoglucanase activity, in addition to beta-glucosidase and cellobiohydrolase activity, present. Reducing sugars were readily released from medium-viscosity carboxymethylcellulose (CMC), but neither CMC, cellulose filter strips, Avicel, cellobiose, nor D-glucose served as the sole carbon source for growth of Azoarcus spp. Clones from a plasmid library of strain BH72 expressed all three enzymes in Escherichia coli, apparently not from their own promoter. According to restriction endonuclease mapping and subclone analysis, beta-glucosidase and cellobiohydrolase activities were localized on a single 2.6-kb fragment not physically linked to a 1.45-kb fragment from which endoglucanase (egl) was expressed. Two isoenzymes of endoglucanase probably resulting from proteolytic cleavage had pI values of 6.4 and 6.1 and an apparent molecular mass of approximately 36 kDa. Cellobiohydrolase and beta-glucosidase activity were conferred by one enzyme 41 kDa in size with a pI of 5.4, which we classified as an unspecific exoglycanase (exg) according to substrate utilization and specificity mapping; hydrolysis of various oligomeric substrates differentiated it from endoglucanase, which degraded substituted soluble cellulose derivatives but not microcrystalline cellulose. Both enzymes were not excreted but were associated with the surface of Azoarcus cells. Both activities were only slightly influenced by the presence of CMC or D-glucose in the growth medium but were enhanced by ethanol. egl was located on a large transcript approximately 15 kb in size, which was detectable only in cells grown under microaerobic conditions on N2. Surface-bound exo- and endoglucanases with some unusual regulatory features, detected in this study in a strain which is unable to metabolize cellulose or sugars, might assist Azoarcus sp. strain BH72 in infection of grass roots.
我们筛选了与草相关的固氮菌新属(固氮弧菌属菌种)的成员,以检测其是否存在纤维素分解酶。在代表不同物种的5株固氮弧菌菌株中,只有根内圈分离株BH72(该菌株也能够侵入草根)除了具有β-葡萄糖苷酶和纤维二糖水解酶活性外,还具有显著的内切葡聚糖酶活性。还原糖很容易从中等粘度的羧甲基纤维素(CMC)中释放出来,但CMC、纤维素滤纸条、微晶纤维素、纤维二糖或D-葡萄糖都不能作为固氮弧菌属菌种生长的唯一碳源。来自菌株BH72质粒文库的克隆在大肠杆菌中表达了所有三种酶,显然不是从它们自己的启动子表达的。根据限制性内切酶图谱和亚克隆分析,β-葡萄糖苷酶和纤维二糖水解酶活性定位在一个2.6kb的单一片段上,该片段与表达内切葡聚糖酶(egl)的1.45kb片段没有物理连接。可能由蛋白水解切割产生的两种内切葡聚糖酶同工酶的pI值分别为6.4和6.1,表观分子量约为36kDa。纤维二糖水解酶和β-葡萄糖苷酶活性由一种大小为41kDa、pI为5.4的酶赋予,根据底物利用和特异性图谱,我们将其归类为非特异性外切聚糖酶(exg);各种寡聚底物的水解将其与内切葡聚糖酶区分开来,内切葡聚糖酶降解取代的可溶性纤维素衍生物但不降解微晶纤维素。这两种酶都不分泌,而是与固氮弧菌细胞表面相关。两种酶的活性仅略微受到生长培养基中CMC或D-葡萄糖存在的影响,但乙醇可增强其活性。egl位于一个大小约为15kb的大转录本上,该转录本仅在微需氧条件下在N2上生长的细胞中可检测到。在本研究中,在一株无法代谢纤维素或糖类的菌株中检测到具有一些不寻常调节特征的表面结合外切和内切葡聚糖酶,它们可能有助于固氮弧菌BH72菌株感染草根。