Woosley Bryan D, Kim Young Hwan, Kumar Kolli V S, Wells Lance, King Dan, Poe Ryan, Orlando Ron, Bergmann Carl
Complex Carbohydrate Research Center, Department of Biochemistry and Molecular Biology, University of Georgia, 315 Riverbend Road, Athens, GA 30602-4712, USA.
Carbohydr Res. 2006 Oct 16;341(14):2370-8. doi: 10.1016/j.carres.2006.06.006. Epub 2006 Jul 18.
The enzyme endo-polygalacturonase A, or PGA, is produced by the fungus, Aspergillus niger, and appears to play a critical role during invasion of plant cell walls. The enzyme has been homologously overexpressed in order to provide sufficient quantities of purified enzyme for structural and biological studies. We have characterized this enzyme in terms of its post-translational modifications (PTMs) and found it to be both N- and O-glycosylated. Additionally, we have characterized the glycosyl moieties using MALDI-TOF and LC-ESI mass spectrometry. The characterization of all PTMs on PGA, along with molecular modeling, allows us to reveal potential roles played by the glycans in modulating the interaction of the enzyme with other macromolecules.
内切多聚半乳糖醛酸酶A(endo-polygalacturonase A,简称PGA)由黑曲霉(Aspergillus niger)产生,在侵袭植物细胞壁的过程中似乎起着关键作用。为了获得足够量的纯化酶用于结构和生物学研究,该酶已被同源过表达。我们已经对这种酶的翻译后修饰(PTM)进行了表征,发现它同时进行了N-糖基化和O-糖基化。此外,我们使用基质辅助激光解吸电离飞行时间质谱(MALDI-TOF)和液相色谱-电喷雾电离质谱(LC-ESI)对糖基部分进行了表征。对PGA上所有PTM的表征以及分子建模,使我们能够揭示聚糖在调节该酶与其他大分子相互作用中所起的潜在作用。