Department of Molecular Microbiology and Biotechnology, Tel Aviv University, Tel Aviv, Israel.
PLoS One. 2013;8(2):e56138. doi: 10.1371/journal.pone.0056138. Epub 2013 Feb 14.
Ruminococcus flavefaciens is one of the predominant fiber-degrading bacteria found in the rumen of herbivores. Bioinformatic analysis of the recently sequenced genome indicated that this bacterium produces one of the most intricate cellulosome systems known to date. A distinct ORF, encoding for a multi-modular protein, RflaF_05439, was discovered during mining of the genome sequence. It is composed of two tandem modules of currently undefined function that share 45% identity and a C-terminal X-dockerin modular dyad. Gaining insight into the diversity, architecture and organization of different types of proteins in the cellulosome system is essential for broadening our understanding of a multi-enzyme complex, considered to be one of the most efficient systems for plant cell wall polysaccharide degradation in nature.
METHODOLOGY/PRINCIPAL FINDINGS: Following bioinformatic analysis, the second tandem module of RflaF_05439 was cloned and its selenium-labeled derivative was expressed and crystallized. The crystals belong to space group P21 with unit-cell parameters of a = 65.81, b = 60.61, c = 66.13 Å, β = 107.66° and contain two protein molecules in the asymmetric unit. The crystal structure was determined at 1.38-Å resolution by X-ray diffraction using the single-wavelength anomalous dispersion (SAD) method and was refined to Rfactor and Rfree of 0.127 and 0.152 respectively. The protein molecule mainly comprises a β-sheet flanked by short α-helixes, and a globular α-helical domain. The structure was found to be structurally similar to members of the NlpC/P60 superfamily of cysteine peptidases.
CONCLUSIONS/SIGNIFICANCE: The 3D structure of the second repeat of the RflaF_05439 enabled us to propose a role for the currently undefined function of this protein. Its putative function as a cysteine peptidase is inferred from in silico structural homology studies. It is therefore apparent that cellulosomes integrate proteins with other functions in addition to the classic well-defined carbohydrate active enzymes.
瘤胃球菌(Ruminococcus flavefaciens)是反刍动物瘤胃中主要的纤维降解菌之一。对最近测序的基因组进行生物信息学分析表明,该细菌产生了迄今为止已知的最复杂的细胞体系统之一。在挖掘基因组序列时,发现了一个独特的 ORF,该 ORF 编码一种多模块蛋白,RflaF_05439。它由两个串联模块组成,目前功能尚未定义,具有 45%的同源性和 C 端 X 结构域模块二联体。深入了解细胞体系统中不同类型蛋白质的多样性、结构和组织对于拓宽我们对多酶复合物的理解至关重要,该复合物被认为是自然界中降解植物细胞壁多糖最有效的系统之一。
方法/主要发现:经过生物信息学分析,克隆了 RflaF_05439 的第二个串联模块,并表达和结晶了其硒标记衍生物。该晶体属于 P21 空间群,具有 a=65.81、b=60.61、c=66.13 Å、β=107.66°的单位细胞参数,在不对称单元中包含两个蛋白质分子。该晶体结构通过使用单波长异常分散(SAD)方法的 X 射线衍射在 1.38-Å 分辨率下确定,并分别精修至 R 因子和 R 自由因子为 0.127 和 0.152。该蛋白质分子主要由β-折叠构成,两侧为短α-螺旋,还有一个球形α-螺旋结构域。该结构被发现与半胱氨酸肽酶的 NlpC/P60 超家族的成员在结构上相似。
结论/意义:RflaF_05439 的第二个重复结构的 3D 结构使我们能够提出该蛋白目前未定义功能的作用。通过计算机结构同源性研究推断其可能作为半胱氨酸肽酶的功能。因此,很明显,细胞体除了经典的明确碳水化合物活性酶之外,还整合了具有其他功能的蛋白质。