Chair of Microbiology, TUM School of Life Sciences, Technical University of Munich, Freising, Germany.
Plant Development, Biozentrum, Ludwig-Maximilans-Universität München, Planegg-Martinsried, Germany.
Appl Environ Microbiol. 2022 Apr 12;88(7):e0246021. doi: 10.1128/aem.02460-21. Epub 2022 Mar 23.
Cellulose is the most abundant biopolymer on earth and offers versatile applicability in biotechnology. Bacterial cellulose, especially, is an attractive material because it represents pure microcrystalline cellulose. The cellulose synthase complex of acetic acid bacteria serves as a model for general studies on (bacterial) cellulose synthesis. The genome of Komagataeibacter hansenii ATCC 23769 encodes three cellulose synthase (CS) operons of different sizes and gene compositions. This implies the question of which role each of the three CS-encoding operons, , , and , plays in overall cellulose synthesis. Therefore, we constructed markerless deletions in ATCC 23769, yielding mutant strains that expressed only one of the three CSs. Apparently, BcsAB1 is the only CS that produces fibers of crystalline cellulose. The markerless deletion of resulted in a nonfiber phenotype in scanning electron microscopy analysis. Expression of the other CSs resulted in a different, nonfibrous extracellular polymeric substance (nfEPS) structure wrapping the cells, which is proposed to contain acetylated cellulose. Transcription analysis revealed that all CSs were expressed continuously and that showed a higher transcription level than . Moreover, we were able to link the expression of diguanylate cyclase B () to cellulose production. Acetic acid bacteria form a massive biofilm called "mother of vinegar," which is built of cellulose fibers. Bacterial cellulose is an appealing biomaterial with manifold applications in biomedicine and biotechnology. Because most cellulose-producing acetic acid bacteria express several cellulose synthase operons, a deeper understanding of their contribution to the synthesis of modified forms of cellulose fibers within a natural biofilm is of special interest. For the first time, we were able to identify the contribution of each of the three cellulose synthases to cellulose formation in Komagataeibacter hansenii ATCC 23769 after a chromosomal clean deletion. Moreover, we were able to depict their roles in spatial composition of the biofilm. These findings might be applicable in the future for naturally modified biomaterials with novel properties.
纤维素是地球上最丰富的生物聚合物,在生物技术中有广泛的应用。特别是细菌纤维素,因为它代表纯微晶纤维素,所以是一种有吸引力的材料。醋酸菌的纤维素合酶复合物是研究(细菌)纤维素合成的一般模型。Komagataeibacter hansenii ATCC 23769 的基因组编码三个大小和基因组成不同的纤维素合酶(CS)操纵子。这就提出了一个问题,即这三个 CS 编码操纵子、、和在整体纤维素合成中各自扮演什么角色。因此,我们在 ATCC 23769 中构建了无标记缺失,产生了只表达三个 CS 中的一个的突变株。显然,BcsAB1 是唯一产生结晶纤维素纤维的 CS。缺失导致扫描电子显微镜分析中出现无纤维表型。其他 CS 的表达导致一种不同的、无纤维的细胞外聚合物物质(nfEPS)结构包裹细胞,据推测该物质含有乙酰化纤维素。转录分析显示所有 CS 都连续表达,并且表现出比更高的转录水平。此外,我们能够将双鸟苷酸环化酶 B () 的表达与纤维素产生联系起来。醋酸菌形成一种叫做“醋母”的巨大生物膜,由纤维素纤维组成。细菌纤维素是一种有吸引力的生物材料,在生物医学和生物技术中有多种应用。由于大多数产生纤维素的醋酸菌表达几个纤维素合酶操纵子,因此深入了解它们对天然生物膜中修饰形式的纤维素纤维合成的贡献具有特殊意义。我们首次在 Komagataeibacter hansenii ATCC 23769 中通过染色体清洁缺失鉴定了三个纤维素合酶中的每一个对纤维素形成的贡献。此外,我们能够描绘它们在生物膜空间组成中的作用。这些发现可能在未来对具有新特性的天然改性生物材料具有应用价值。