Isolation, screening, and molecular identification of pectinase producers from fruits, vegetables, and soil samples

IF 0.7 Q4 PHARMACOLOGY & PHARMACY Egyptian Pharmaceutical Journal Pub Date : 2022-07-01 DOI:10.4103/epj.epj_39_22
Abdullin Kh, A. Attallah, N. Abdel-Aziz, Bigad E. Khalil
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引用次数: 1

Abstract

Background and objective In this work, isolation, identification (morphological and chemical), and molecular characterization were done of local isolates of some pectinase-producing microorganisms such as bacteria, actinomycetes, fungi, and yeast. Materials and methods A total of 22 local bacterial isolates were obtained from various sources and were assayed for pectinolytic activity after optimization of conditions for pectinase production. Isolate no. 19 showed the highest pectinase-specific activity (6.73 U/ml) on glucose-supplemented medium, whereas isolate no. 5 gave the lowest pectinase productivity (3.21 U/ml). The identification of isolate no. 19 revealed that it belonged to the genus Bacillus based on morphological and biochemical characteristics. Based on molecular identification (16 S rRNA technique), isolate no. 19 was named Bacillus sp. strain NRBANKI-4 (with 99% similarity), with Gene Bank accession number OM540351. Results and conclusion A total of 14 local actinomycete isolates were obtained from soil samples. Isolate no. 13 showed the highest pectinase-specific activity (6.48 U/ml), whereas sample no. 10 gave the lowest pectinase-specific activity (3.07 U/ml). Based on molecular identification (16 S rRNA technique), isolate no. 13 was named Streptomyces sp. KP 12 (90.63% similarity), with Gene Bank accession number OM403596. A total of 10 fungal isolates were obtained from crop waste soil. Isolate no. 2 gave the highest pectinase productivity (21.20 U/ml). Based on molecular identification (internal transcribed spacer-PCR technique), isolate no. 2 was named Aspergillus niger F8121 (99.47% similarity), with Gene Bank accession number OM392061. Following the same trend, 10 yeast isolates were isolated from crop waste soil. The isolate that gave the highest pectinase productivity was no. 7, which gave 22.03 U/ml. The isolate that gave the lowest was no. 9 (20.74 U/ml). Isolate no. 7 was named Pichia barkeri Y1 (90.91% similarity), with Gene Bank accession number OM392066.
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从水果、蔬菜和土壤样品中分离、筛选和鉴定果胶酶产生物
背景与目的对细菌、放线菌、真菌和酵母菌等产果胶酶微生物进行了分离、形态、化学鉴定和分子鉴定。材料与方法从不同来源获得22株本地分离菌,优化生产果胶酶的条件,测定其果胶溶酶活性。没有隔离。菌株19在葡萄糖添加培养基上的果胶酶特异性活性最高,为6.73 U/ml;5株果胶酶产率最低,为3.21 U/ml。分离物编号的鉴定。19 .根据形态和生化特征,显示它属于芽孢杆菌属。基于分子鉴定(16s rRNA技术),分离得到1。其中19株被命名为芽孢杆菌菌株NRBANKI-4(相似性为99%),基因库登录号为OM540351。结果与结论从土壤样品中分离到14株放线菌。没有隔离。13株果胶酶特异性活性最高,为6.48 U/ml;10株果胶酶特异性活性最低,为3.07 U/ml。基于分子鉴定(16s rRNA技术),分离得到1。其中13株被命名为Streptomyces sp. KP 12(相似性为90.63%),其基因库登录号为OM403596。从农作物废土中分离得到10株真菌。没有隔离。2的果胶酶产率最高,为21.20 U/ml。基于分子鉴定(内转录间隔期pcr技术),分离得到1号。其中2株被命名为黑曲霉F8121(相似度99.47%),基因库登录号为OM392061。从农作物废土中分离出10株酵母菌。果胶酶产率最高的菌株为no。结果为22.03 U/ml。给出最低的分离物是no。9 (20.74 U/ml)。没有隔离。其中7株命名为巴氏毕赤酵母Y1(相似性为90.91%),基因库登录号为OM392066。
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来源期刊
Egyptian Pharmaceutical Journal
Egyptian Pharmaceutical Journal PHARMACOLOGY & PHARMACY-
CiteScore
1.10
自引率
0.00%
发文量
37
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