Investigation on the activity of purified inulinase enzymes from fungal strains on the inulin extracted from chicory (Cichorium intybus) for production of fructose sweetener

International Journal of Molecular and Clinical Microbiology

دوره 12، شماره 2، بهمن 2022، صفحه 1729-1739   

نوع مقاله: Research Article

شناسه دیجیتال (DOI): 10.22034/ijmcm.2022.694916

نویسندگان

Faezeh Abedi¹؛ Nafiseh Sadat Naghavi^{* 1}؛ Monireh Ranjbar²

¹Department of Microbiology, Falavarjan Branch, Islamic Azad University, Isfahan, Iran

²Department of Biology, Falavarjan Branch, Islamic Azad University, Isfahan, Iran

چکیده

Chicory is a rich plant source for the prebiotic inulin. The aim of this study was to evaluate the activity of purified inulinase enzyme from fungal strains on the inulin extracted from chicory. Inulin was extracted by soaking in water and precipitating in ethanol. Fungi were isolated from the soil around chicory root and screened for inulinase production along with fungal strains, Kluyveromyces marxianus PTCC 5006 and Aspergillus flavus PTCC 5304. The high inulinase-producing fungal isolate was identified based on the sequencing of 18S rRNA gene. The enzyme was purified using ammonium sulfate-polyacrylamide and dialysis. The molecular weight of the protein was detected using sodium dodecyl sulfate polyacrylamide gel electrophoresis (SDS-PAGE). One fungal isolate that showed high enzymatic activity (2233 U/ml) was obtained. This isolate was identified as the species Talaromyces moniliformis. Among the collection strains, Kluyveromyces marxianus had the highest inulinase production; while its inulinase activity was lower than that of Talaromyces moniliformis. The results from enzyme purification from Talaromyces moniliformis showed that the most specific enzyme activity (546.6 U/mg) and the highest purification yield (62.17%) were obtained by the precipitation in 55% ammonium sulfate. Dialysis of the protein resulted in the extraction of a protein with a reduced specific enzyme activity (188.6 U/mg). The molecular weight of the purified protein was estimated at15 kDa.The fungal inulinase which purified from native resources in the present study can be used in food and pharmaceutical industries due to its high enzymatic activity.

کلیدواژه‌ها

Inulin؛ Chicory؛ Inulinase؛ Fungal strains؛ Enzyme purification