Rehman Haneef Ur, Siddique Nadir Naveed, Aman Afsheen, Nawaz Muhammad Asif, Baloch Abdul Hameed, Qader Shah Ali Ul
Faculty of Agriculture, Lasbela University of Agriculture, Water and Marine Sciences (LUAWMS), Uthal, Balochistan, 90150, Pakistan.
The Karachi Institute of Biotechnology and Genetic Engineering (KIBGE), University of Karachi, Karachi 75270, Pakistan.
J Genet Eng Biotechnol. 2015 Dec;13(2):139-144. doi: 10.1016/j.jgeb.2015.07.004. Epub 2015 Aug 8.
Pectinase catalyzed the degradation of pectin substances and has been used in various biotechnological industries. In the current study, 23 bacterial strains were isolated from rotten vegetables, soil and air. The isolated bacterial strains were qualitatively screened for pectinase production on pectin agar medium and only three strains HR 4, HR 21 and HR 23 were observed to produce extracellular pectinase. These strains were further screened quantitatively for pectinase production through submerged fermentation technology in pectin containing fermentation medium. Strain HR 4 from rotten brinjal () was found to produce higher pectinase as compared to others. The maximum pectinase producing bacterial strain was identified as on the basis of morphological, physiological and biochemical characteristics. For further confirmation of identification, 16S rDNA sequence analysis was performed. The 16S rDNA sequences were aligned and the phylogenetic tree was constructed. The phylogenetic tree confirmed that the strain was belonging to . The 16S rDNA sequences of this new strain were submitted to GenBank and designated as KIBGE-IB21 with the GenBank accession number JQ 411812. The newly isolated pectinase producing used apple pectin as carbon and yeast extract as nitrogen source for maximum pectinase production.
果胶酶催化果胶物质的降解,已被应用于各种生物技术产业。在本研究中,从腐烂蔬菜、土壤和空气中分离出23株细菌菌株。在果胶琼脂培养基上对分离出的细菌菌株进行果胶酶产生的定性筛选,仅观察到三株菌株HR 4、HR 21和HR 23产生细胞外果胶酶。通过在含果胶的发酵培养基中采用深层发酵技术对这些菌株进行果胶酶产生的定量筛选。发现来自腐烂茄子的HR 4菌株比其他菌株产生更高的果胶酶。根据形态、生理和生化特征,将产生果胶酶最多的细菌菌株鉴定为 。为进一步确认鉴定结果,进行了16S rDNA序列分析。对16S rDNA序列进行比对并构建系统发育树。系统发育树证实该菌株属于 。将该新菌株的16S rDNA序列提交至GenBank,并命名为 KIBGE - IB21,GenBank登录号为JQ 411812。新分离出的产果胶酶 以苹果果胶作为碳源,酵母提取物作为氮源以实现最大果胶酶产量。