SoyProDB: A database for the identification of soybean seed proteins.

UNLABELLED: Soybean continues to serve as a rich and inexpensive source of protein for humans and animals. A substantial amount of information has been reported on the genotypic variation and beneficial genetic manipulation of soybeans. For better understanding of the consequences of genetic manipulation, elucidation of soybean protein composition is necessary, because of its direct relationship to phenotype. We have conducted studies to determine the composition of storage, allergen and anti-nutritional proteins in cultivated soybean using a combined proteomics approach. Two-dimensional polyacrylamide gel electrophoresis (2DPAGE) was implemented for the separation of proteins along with matrix-assisted laser desorption/ionization time of flight mass spectrometry (MALDI-TOF-MS) and liquid chromatography mass spectrometry (LC-MS/MS) for the identification of proteins. Our analysis resulted in the identification of several proteins, and a web based database named soybean protein database (SoyProDB) was subsequently built to house and allow scientists to search the data. This database will be useful to scientists who wish to genetically alter soybean with higher quality storage proteins, and also helpful for consumers to get a greater understanding about proteins that compose soy products available in the market. The database is freely accessible. AVAILABILITY: http://bioinformatics.towson.edu/Soybean_Seed_Proteins_2D_Gel_DB/Home.aspx.

Background

Soybean is the second most valuable agricultural commodity and an inexpensive source of proteins for humans and animals in the United States. Soybean seed proteins possess unique physiochemical properties which are suitable for various human and animal food uses. Soybean seed proteins are used in baby formula, flour, protein supplements, concentrates, and textured fibers. Soybean seeds contain 40-50% protein on a dry matter basis and consist predominantly of globulin type of proteins. Soybean storage proteins account for ~70-80% of total seed proteins and are deposited in protein bodies, which are specialized membrane-bound organelles. These storage proteins are largely responsible for the nutritional and physicochemical properties of soybeans. Soybeans are also sources of several secondary metabolites including isoflavones, saponins, phytic acid, flatus-producing oligosaccharides, and goitrogens.

In recent years, the application of proteomic tools such as twodimensional polyacrylamide gel electrophoresis, matrixassisted laser desorption/ionization time of flight, and liquid chromatography mass spectrometry, has become popular as a powerful methodology for accurately detecting and examining changes in protein composition. These tools have been extensively used to examine the composition of both natural and transgenic soybean storage protein profiles and determine seed qualities of soybeans. Information about soybean seed proteins will be useful for scientists to understand their functional characteristics for subsequent modification of the protein through genetic alteration in order to obtain a valuable trait. However limited sources are available to retrieve soybean protein information from publicly available databases [1, 2]. Therefore, we developed a database for soybean seed proteins which are easily accessible to the scientific community as well as the general public.

Identified Soybean Proteins:

The majority of the proteins described in our database are in the form of storage, allergen, and anti-nutritional. β-conglycinin, one of the two major storage proteins, is a trimeric 7S globulin glycoprotein consisting of three types of subunits: α, α′ and β, in seven different combinations with the molecular weight of 180 kDa. The second storage protein, glycinin, is a hexameric 11S globulin (360 kDa), consists of acidic (A) and basic (B) polypeptides, and is encoded by five subunits. Based on physical properties, these five subunits are classified into two distinct major groups; group I consisting of G1, G2, and G3 proteins, and group II consisting G4 and G5 subunits. The group I subunits contain more methionine residues than group II. This is an important feature for plant breeders desiring to increase the methionine content in soybean seeds to improve their nutritional quality. Beillinson et al. [3] identified and mapped two additional genes in soybean variety Resnik. The soybean allergen proteins exist as three major types. The first major allergen, soybean Gly m Bd 60K, is described as seed storage protein. Based on the many reports, some subunits of β- conglycinin and glycinin are considered as Gly m Bd 60k allergen protein members. Krishnan et al. [4] reported that all subunits of β-conglycinin are possible allergens. Gly m Bd 30K is the second major allergen protein of soybean.

This protein was previously described in soybean seed as P34, a 34-kD vacuolar protein [5]. Elimination of P34 from soybean seeds may enhance food safety and make the use of soybean products available to sensitive individuals. Recently, Herman et al. [6] developed a transgenic soybean lacking p34 allergen. The third allergen, Gly m Bd 28K is a less abundant protein of soybean which was originally isolated from soybean meal as a 28 kDa glycosylated protein [7]. Like allergens, anti-nutritional proteins in soybean act as limiters for soybean applications as a food or feed. Kunitz trypsin inhibitor (KTI) is one of the abundant anti-nutritional proteins, which can inhibit trypsin, an important animal digestive enzyme. In addition, KTIs have been characterized as food allergens in humans and have 32% sequence homology with a rye grass pollen allergen [8]. Seed lectins are also anti-nutritional proteins present in soybeans and account for about 10% of total protein in some legumes.

Methodology

Protein was extracted from cultivated soybean seed, G. max PI 423954. Extraction procedures used were a modified TCA/acetone method and isopropanal method [9, 10]. 2DPAGE separation was performed using IPG strips with pH 3.0- 10.0, 4.0-7.0 and 6.0 -11 ranges. Protein spots were initially analyzed by MALDI-TOF-MS, and those not positively identified were subjected to LC-MS/MS. Protein identification was performed by searching against National Center for Biotechnology Information (NCBI) non-redundant database using the Mascot search engine (http://www.matrixscience.com). The identified proteins were classified in to 3 major protein groups: storage, allergen, and anti-nutritional.

Database methodology:

The web based database is composed of two main parts. The first one is a relational database built on Access 2007. The second part is the web interface. Web pages were created using Active Server Pages (ASP.Net) using C# programming language. Both the database and the interface are housed on the bioinformatics server at Towson University, MD, USA. The site houses several 2D Gel images showing isolated soybean seed proteins. Each protein is given a unique number (SpotID). Information on each protein on the gels is stored in the database. The website allows users to enter the SpotID for the protein of interest, and retrieves the corresponding information on that protein from the SoyProDB. The design is simple, yet efficient, and meets the needs of the biologists using the database. Figure 1 is a snapshot of the database's main page. The database is accessible from: http://bioinformatics.towson.edu/Soybean_Seed_Proteins_2D _Gel_DB /Home.aspx.

Utility of the biological community

The database is of interest to biologists working with soybeans and/or seed proteins. It provides an easy and visual means to identify key proteins in soybean seeds. The web interface allows scientists to access the data using any web browser.

Caveats

More gels need to be added to this database as well as a more comprehensive biological interpretation of the data. Work on that is underway.