Assessment of cultivation parameters influencing pectinase production by Aspergillus niger LFP-1 in submerged fermentation.

IF 3.6 Q2 BIOTECHNOLOGY & APPLIED MICROBIOLOGY Journal, genetic engineering & biotechnology Pub Date : 2023-04-24 DOI:10.1186/s43141-023-00510-z
Mohd Taufiq Mat Jalil, Nurul Aili Zakaria, Nor Hawani Salikin, Darah Ibrahim
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Abstract

Background: Pectinase is helpful in food and beverage industries, particularly in the preparation of fruit juice, the extraction of vegetable oil, and the fermentation of coffee. The current work aimed to screen Aspergillus niger LFP-1, a recently identified fungal strain, for its ability to produce pectinase and to ascertain the contribution of various physicochemical factors to pectinase production.

Results: The primary and secondary pectinase activity screenings by Aspergillus niger LFP-1 were performed using pectin screening agar and shake flask system, respectively. The finding revealed that the locally isolated strain is able to secrete favourable pectinase production. Before improvement, the pectinase production was 0.88 ± 0.09 U/mL. However, the improved conditions such as 6 days of the cultivation period, agitation speed of 150 rpm, inoculum size of 1 × 106 spores/mL, 2.5% (w/v) citrus pectin, and 0.4% (w/v) ammonium nitrate could significantly increase pectinase production up to 7.41 ± 0.24 U/mL, representing an 88% increase. In this study, supplementing 2.5% (w/v) citrus pectin to the culture medium as a carbon source increased enzyme production by up to 3.07 ± 0.17 U/mL. Meanwhile, 0.4% (w/v) ammonium nitrate was used as a nitrogen source yielding the highest enzyme activity with a value of 6.86 ± 0.07 U/mL.

Conclusion: Thus, the locally isolated fungal strain, A. niger LFP-1 has outstanding pectinase-producing capability and can be utilized for the commercial production of pectinase. The improved cultural conditions significantly increase pectinase production and shorten the incubation period from 8 days (before improvement) to 6 days (after improvement).

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培养参数对黑曲霉LFP-1深层发酵产胶酶影响的评价。
背景:果胶酶在食品和饮料工业中很有帮助,特别是在果汁的制备、植物油的提取和咖啡的发酵中。目前的工作旨在筛选黑曲霉LFP-1,一种新发现的真菌菌株,其生产果胶酶的能力,并确定各种理化因素对果胶酶生产的贡献。结果:分别采用果胶筛选琼脂和摇瓶系统对黑曲霉LFP-1进行了初级和二级果胶酶活性筛选。研究结果表明,局部分离的菌株能够分泌有利的果胶酶生产。改进前的果胶酶产率为0.88±0.09 U/mL。而在培养时间为6 d、搅拌速度为150 rpm、接种量为1 × 106孢子/mL、柑橘果胶用量为2.5% (w/v)、硝酸铵用量为0.4% (w/v)的条件下,果胶酶产量显著提高,达到7.41±0.24 U/mL,提高了88%。在本研究中,在培养基中添加2.5% (w/v)柑橘果胶作为碳源,可使酶产量提高3.07±0.17 U/mL。以0.4% (w/v)硝酸铵为氮源,酶活最高,为6.86±0.07 U/mL。结论:该局部分离菌株黑曲霉LFP-1具有良好的生产果胶酶的能力,可用于果胶酶的商业化生产。改进后的培养条件显著提高了果胶酶的产量,并将培养时间从改进前的8天缩短到改进后的6天。
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