Oleas Gabriela, Callegari Eduardo, Sepúlveda Romina, Eyzaguirre Jaime
Facultad de Ciencias Biológicas, Universidad Andrés Bello, Santiago, Chile.
BRIN-USDSSOM Proteomics Facility, University of South Dakota, Vermillion, SD, USA.
Carbohydr Res. 2017 Apr 18;443-444:42-48. doi: 10.1016/j.carres.2017.03.014. Epub 2017 Mar 18.
The lignocellulolytic fungus, Penicillium purpurogenum, grows on a variety of natural carbon sources, among them sugar beet pulp. Culture supernatants of P. purpurogenum grown on sugar beet pulp were partially purified and the fractions obtained analyzed for esterase activity by zymograms. The bands with activity on methyl umbelliferyl acetate were subjected to mass spectrometry to identify peptides. The peptides obtained were probed against the proteins deduced from the genome sequence of P. purpurogenum. Eight putative esterases thus identified were chosen for future work. Their cDNAs were expressed in Pichia pastoris. The supernatants of the recombinant clones were assayed for esterase activity, and five of the proteins were active against one or more substrates: methyl umbelliferyl acetate, indoxyl acetate, methyl esterified pectin and fluorescein diacetate. Three of those enzymes were purified, further characterized and subjected to a BLAST search. Based on their amino acid sequence and properties, they were identified as follows: RAE1, pectin acetyl esterase (CAZy family CE 12); FAEA, feruloyl esterase (could not be assigned to a CAZy family) and EAN, acetyl esterase (former CAZy family CE 10).
木质纤维素分解真菌产紫青霉能在多种天然碳源上生长,其中包括甜菜粕。以甜菜粕为碳源培养产紫青霉,其培养上清液经部分纯化后,通过酶谱分析对所得组分的酯酶活性进行检测。对在乙酸甲基伞形酯上有活性的条带进行质谱分析以鉴定肽段。将所得肽段与产紫青霉基因组序列推导的蛋白质进行比对。由此鉴定出的8种假定酯酶被选作后续研究对象。它们的cDNA在巴斯德毕赤酵母中表达。对重组克隆的上清液进行酯酶活性检测,其中5种蛋白质对一种或多种底物有活性:乙酸甲基伞形酯、乙酸吲哚酚、甲基酯化果胶和二乙酸荧光素。对其中3种酶进行了纯化、进一步表征并进行了BLAST搜索。根据它们的氨基酸序列和性质,鉴定结果如下:RAE1,果胶乙酰酯酶(碳水化合物活性酶家族CE 12);FAEA,阿魏酸酯酶(无法归入碳水化合物活性酶家族);EAN,乙酰酯酶(原碳水化合物活性酶家族CE 10)。