4.7 Article

A Single Seed Protein Extraction Protocol for Characterizing Brassica Seed Storage Proteins

期刊

AGRONOMY-BASEL
卷 11, 期 1, 页码 -

出版社

MDPI
DOI: 10.3390/agronomy11010107

关键词

protein extraction; seed proteins; Brassica rapa; 2S albumin like napins; 11; 12S globulin like cruciferins; 1D SDS-PAGE; EMS mutant population

资金

  1. International Postgraduate Research Scholarship (IPRS)
  2. Australian Postgraduate Award (APA) scholarship - Australian Government

向作者/读者索取更多资源

This study focused on isolating and measuring proteins in rapeseed oil-extracted expeller cake to maximize protein yield while minimizing hazardous chemical use and extraction costs. By testing various extraction methods, a standardized Single Rapeseed Seed Protein Extraction (SRPE) procedure was developed, providing an efficient and economical way to extract seed storage proteins. The optimized method was validated by applying it to different Brassica oilseeds and an ethyl methane sulfonate mutant population, demonstrating its usefulness in identifying and characterizing seed storage proteins.
Rapeseed oil-extracted expeller cake mostly contains protein. Various approaches have been used to isolate, detect and measure proteins in rapeseeds, with a particular focus on seed storage proteins (SSPs). To maximize the protein yield and minimize hazardous chemical use, isolation costs and the loss of seed material, optimization of the extraction method is pivotal. For some studies, it is also necessary to minimize or avoid seed-to-seed cross-contamination for phenotyping and single-tissue type analysis to know the exact amount of any bioactive component in a single seed, rather than a mixture of multiple seeds. However, a simple and robust method for single rapeseed seed protein extraction (SRPE) is unavailable. To establish a strategy for optimizing SRPE for downstream gel-based protein analysis, yielding the highest amount of SSPs in the most economical and rapid way, a variety of different approaches were tested, including variations to the seed pulverization steps, changes to the compositions of solvents and reagents and adjustments to the protein recovery steps. Following SRPE, 1D-SDS-PAGE was used to assess the quality and amount of proteins extracted. A standardized SRPE procedure was developed and then tested for yield and reproducibility. The highest protein yield and quality were obtained using a ball grinder with stainless steel beads in Safe-Lock microcentrifuge tubes with methanol as the solvent, providing a highly efficient, economic and effective method. The usefulness of this SRPE was validated by applying the procedure to extract protein from different Brassica oilseeds and for screening an ethyl methane sulfonate (EMS) mutant population of Brassica rapa R-0-18. The outcomes provide useful methodology for identifying and characterizing the SSPs in the SRPE.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.7
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据