Plant Pathology Section, Sugarcane Breeding Institute, Indian Council of Agricultural Research, Tamil Nadu, India.
Electrophoresis. 2010 Jun;31(12):1959-74. doi: 10.1002/elps.200900779.
Sugarcane is an important commercial crop cultivated for its stalks and sugar is a prized commodity essential in human nutrition. Proteomics of sugarcane is in its infancy, especially when dealing with the stalk tissues, where there is no study to date. A systematic proteome analysis of stalk tissue yet remains to be investigated in sugarcane, wherein the stalk tissue is well known for its rigidity, fibrous nature, and the presence of oxidative enzymes, phenolic compounds and extreme levels of carbohydrates, thus making the protein extraction complicated. Here, we evaluated five different protein extraction methods in sugarcane stalk tissues. These methods are as follows: direct extraction using lysis buffer (LB), TCA/acetone precipitation followed by solubilization in LB, LB containing thiourea (LBT), and LBT containing tris, and phenol extraction. Both quantitative and qualitative protein analyses were performed for each method. 2-DE analysis of extracted total proteins revealed distinct differences in protein patterns among the methods, which might be due to their physicochemical limitations. Based on the 2-D gel protein profiles, TCA/acetone precipitation-LBT and phenol extraction methods showed good results. The phenol method showed a shift in pI values of proteins on 2-D gel, which was mostly overcome by the use of 2-D cleanup kit after protein extraction. Among all the methods tested, 2-D cleanup-phenol method was found to be the most suitable for producing high number of good-quality spots and reproducibility. In total, 30 and 12 protein spots commonly present in LB, LBT and phenol methods, and LBT method were selected and subjected to eLD-IT-TOF-MS/MS and nESI-LC-MS/MS analyses, respectively, and a reference map has been established for sugarcane stalk tissue proteome. A total of 36 nonredundant proteins were identified. This is a very first basic study on sugarcane stalk proteome analysis and will promote the unexplored areas of sugarcane proteome research.
甘蔗是一种重要的经济作物,其茎秆用于种植,而糖则是人类营养的重要商品。甘蔗的蛋白质组学研究还处于起步阶段,尤其是在处理茎组织方面,目前还没有相关研究。对甘蔗茎组织的系统蛋白质组学分析尚未进行研究,因为甘蔗的茎组织具有刚性、纤维状的特性,并且存在氧化酶、酚类化合物和极高水平的碳水化合物,这使得蛋白质提取变得复杂。在这里,我们评估了五种不同的甘蔗茎组织蛋白质提取方法。这些方法如下:直接使用裂解缓冲液(LB)提取、TCA/丙酮沉淀后再溶解于 LB 中、含硫脲的 LB(LBT)以及含硫脲和三羟甲基氨基甲烷的 LB(LBT)和酚提取。对每种方法都进行了定量和定性蛋白质分析。提取的总蛋白的 2-DE 分析显示,方法之间的蛋白质图谱存在明显差异,这可能是由于其物理化学限制所致。基于 2-DE 凝胶蛋白图谱,TCA/丙酮沉淀-LBT 和酚提取方法显示出良好的效果。酚提取方法在 2-DE 凝胶上显示出蛋白质等电点值的变化,但在蛋白质提取后使用 2-DE 清洗试剂盒可在很大程度上克服这一问题。在所有测试的方法中,发现 2-DE 清洗-酚法最适合产生大量高质量的点和重现性。总共在 LB、LBT 和酚法中以及 LBT 法中都存在 30 和 12 个蛋白质斑点,选择并对这些斑点进行 eLD-IT-TOF-MS/MS 和 nESI-LC-MS/MS 分析,建立了甘蔗茎组织蛋白质组参考图谱。共鉴定出 36 个非冗余蛋白质。这是对甘蔗茎蛋白质组分析的首次基础研究,将促进对甘蔗蛋白质组研究的未知领域的探索。