Journal
BIOCATALYSIS AND AGRICULTURAL BIOTECHNOLOGY
Volume 45, Issue -, Pages -Publisher
ELSEVIER
DOI: 10.1016/j.bcab.2022.102479
Keywords
Glucan phosphatase; Starch degradation; Starch phosphorylation; Starch Excess4; Reversible starch phosphorylation
Categories
Funding
- National Science Foundation [MCB-2012074, CHE-1808304, MCB-1817417]
- Schupf Scholar Program
- Skidmore College start-up funds
- Skidmore Summer Collaborative Research Fellowship
Ask authors/readers for more resources
The study found that different organisms have different glucan phosphatase activity, and the activity is directly correlated with glucan substrate binding and the ability to enhance in vitro starch degradation by beta-amylase BAM3.
The glucan phosphatase Starch EXcess4 (SEX4) plays an essential role in regulating starch degra-dation through reversible phosphorylation. However, starch granule properties and phosphoryla-tion levels vary widely between different organisms. We biochemically characterized SEX4 from agronomically relevant plants and found that SEX4 orthologs display differential glucan phos-phatase activity. SEX4 from cereal crops displayed higher dephosphorylation rates than SEX4 from storage tubers. Intriguingly, these rates were found to be inversely related to glucan sub-strate binding. To determine the effects of this difference, the ability of SEX4 orthologs to en-hance in vitro starch degradation by the beta-amylase BAM3 was measured. An inverse relationship was observed between SEX4 ortholog starch binding affinity and its ability to enhance BAM3-mediated glucan degradation. Collectively, our findings reveal a direct correlation between the dephosphorylation rates of SEX4 orthologs and their ability to enhance in vitro starch degrada-tion. These data provide significant insights into the differential activity of SEX4 from different organisms, corresponding to their distinct biological roles and providing the basis for utilizing their specific properties for industrial and biotechnological applications.
Authors
I am an author on this paper
Click your name to claim this paper and add it to your profile.
Reviews
Recommended
No Data Available