The complete biodegradation pathway of ellagitannins by Aspergillus niger in solid-state fermentation

被引:59
作者
Ascacio-Valdes, Juan A. [1 ]
Aguilera-Carbo, Antonio F. [2 ]
Buenrostro, Jose J. [3 ]
Prado-Barragan, Arely [3 ]
Rodriguez-Herrera, Raul [1 ]
Aguilar, Cristobal N. [1 ]
机构
[1] Univ Autonoma Coahuila, Sch Chem, Dept Food Res, Saltillo, Coahuila, Mexico
[2] Univ Autonoma Agr Antonio Narro, Dept Food Sci & Nutr, Saltillo, Coahuila, Mexico
[3] Univ Autonoma Metropolitana, Unidad Iztapalapa, Dept Biotechnol, Saltillo, Coahuila, Mexico
关键词
Biodegradation; Pathway; Ellagitannins; ELLAGIC ACID PRODUCTION; ANTIOXIDANT ACTIVITY; CRANBERRY POMACE; ACYL HYDROLASE; POMEGRANATE; TANNINS; JUICE; OPTIMIZATION; GH1;
D O I
10.1002/jobm.201500557
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Our research group has found preliminary evidences of the fungal biodegradation pathway of ellagitannins, revealing first the existence of an enzyme responsible for ellagitannins degradation, which hydrolyzes pomegranate ellagitannins and it was called ellagitannase or elagitannin acyl hydrolase. However, it is necessary to generate new and clear information in order to understand the ellagitannin degradation mechanisms. This work describes the distinctive and unique features of ellagitannin metabolism in fungi. In this study, hydrolysis of pomegranate ellagitannins by Aspergillus niger GH1 was studied by solid-state culture using polyurethane foam as support and pomegranate ellagitannins as substrate. The experiment was performed during 36h. Results showed that ellagitannin biodegradation started after 6h of fermentation, reaching the maximal biodegradation value at 18h. It was observed that ellagitannase activity appeared after 6h of culture, then, the enzymatic activity was maintained up to 24h of culture reaching 390.15U/L, after this period the enzymatic activity decreased. Electrophoretic band for ellagitannase was observed at 18h. A band obtained using non-denaturing electrophoresis was identified as ellagitannase, then, a tandem analysis to reveal the ellagitannase activity was performed using Petri plate with pomegranate ellagitannins. The extracts were analyzed by HPLC/MS to evaluate ellagitannins degradation. Punicalin, gallagic acid, and ellagic acid were obtained from punicalagin. HPLC/MS analysis identified the gallagic acid as an intermediate molecule and immediate precursor of ellagic acid. The potential application of catabolic metabolism of ellagitannin hydrolysis for ellagic acid production is outlined.
引用
收藏
页码:329 / 336
页数:8
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