Mahasneh Amjad A, Odat Jazi D, Al-Joubori Ban M, Saadoun Ismail
Department of Biotechnology and Genetic Engineering, Faculty of Science and Arts, Jordan University of Science and Technology, Irbid 22110, Jordan.
Applied Technology High School, Al Ain, Abu Dhabi, United Arab Emirates.
Saudi J Biol Sci. 2021 Aug;28(8):4500-4510. doi: 10.1016/j.sjbs.2021.04.048. Epub 2021 Apr 24.
This investigation aimed to determine the relatedness of dominant occurring soil spp. in Northern Jordan based on their RAPD-PCR fingerprints, and to compare RAPD technique with the conventional phenotypic characterization of isolates. Fifty-eight white and gray color-bearing aerial mycelia antibiotic active-producing soil isolates along with three reference strains were genetically analyzed by RAPD-PCR. Polymorphisms between the isolates showed 1 to 10 bands per isolate and ranged from 200 to 3200 bp in size. Results revealed one common band of ~600 bp shared by ~85% of the isolates, and the observation of bands specific to some reference strains and some soil isolates. When RAPD patterns were analyzed with the UPGMA, results revealed clustering the tested isolates into two equal main super clusters (50% each). Super cluster I appeared to be homogenous and include the three reference strains. However, super cluster II was heterogeneous and but not including any of the reference strains. The association of the antibiotic activity of the dominant white and gray aerial mycelium-bearing isolates to RAPD clustering is reported for the first time, and the RAPD-PCR fingerprints generated here deserve to be cloned, characterized and sequenced in future as species-specific DNA markers. The more random primers used in the analysis may add to RAPD technique a cost-effective, fast, precise result, and less labor work solution for analyzing the similarities and differences among the isolates.
本研究旨在根据约旦北部主要土壤菌种的随机扩增多态性DNA聚合酶链反应(RAPD-PCR)指纹图谱确定它们之间的相关性,并将RAPD技术与分离株的传统表型特征进行比较。通过RAPD-PCR对58株产生白色和灰色气生菌丝且具有抗生素活性的土壤分离株以及3株参考菌株进行了遗传分析。分离株之间的多态性显示每个分离株有1至10条带,大小在200至3200碱基对之间。结果显示约85%的分离株共有一条约600碱基对的共同条带,同时观察到一些参考菌株和一些土壤分离株特有的条带。当用非加权组平均法(UPGMA)分析RAPD图谱时,结果显示将测试的分离株聚为两个相等的主要超级聚类(各占50%)。超级聚类I似乎是同质的,包括3株参考菌株。然而,超级聚类II是异质的,且不包括任何参考菌株。首次报道了占主导地位的白色和灰色气生菌丝分离株的抗生素活性与RAPD聚类的关联,此处产生的RAPD-PCR指纹图谱今后值得作为物种特异性DNA标记进行克隆、表征和测序。分析中使用的随机引物越多,可能会为RAPD技术增添一种经济高效、快速、精确且省力的方法,用于分析分离株之间的异同。