Molecular Detection and Phylogenetic Analysis of the alkB Gene in Klebsiella oxytoca Strains Isolated from the Gut of Tenebrio molitor

Q2 Environmental Science The Scientific World Journal Pub Date : 2024-05-09 DOI:10.1155/2024/3350591
Tsitsi Lynn Mupamhadzi, Oleen Machona, F. Chidzwondo, Rumbidzai Mangoyi
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Abstract

The challenge in polystyrene disposal has caused researchers to look for urgent innovative and ecofriendly solutions for plastic degradation. Some insects have been reported to use polystyrene as their sole carbon source, and this has been linked to the presence of microbes in their guts that aid in plastic digestion. Thus, this study focuses on the molecular detection and phylogenetic analysis of the alkane-1-monooxygenase (alkB) gene in Klebsiella oxytoca strains isolated from the gut of Tenebrio molitor. The alkB gene encodes for alkane-1-monooxygenase, an enzyme involved in the oxidation of inactivated alkanes. This gene can be used as a marker to assess bacteria's ability to biodegrade polystyrene. Three bacterial strains were isolated from the guts of T. molitor mealworms and were confirmed using polymerase chain reaction (PCR) of the 16S ribosomal RNA gene. The primers used in the amplification of the 16S ribosomal RNA region were designed using NCBI, a bioinformatics tool. To detect the presence of the alkB gene in the isolated bacterial strains, a set of primers used in the amplification of this gene was manually designed from the conserved regions of the alkB nucleotide sequences of eleven bacterial species from GenBank. TCOFFE online tool was used to align the alkB sequences of the bacteria, while Jalview and ConSurf were used to view the alignment. The amplified alkB gene was then sequenced using the Sanger sequencing technique, blasted on NCBI to look for similar sequences, and a phylogenetic tree was constructed. Based on the 16S ribosomal RNA gene sequences, the isolated bacterial strains were confirmed to be Klebsiella oxytoca NBRC 102593, Klebsiella oxytoca JCM 1665, and Klebsiella oxytoca ATCC 13182. The alkB gene sequence identical to fourteen alkB gene sequences derived from Actinobacteria whole genome was detected in Klebsiella oxytoca for the first time to the best of our knowledge. The novel nucleotide sequence was published in the NCBI database under accession number OP959069. This gene sequence was found to be for the enzyme alkane-1-monooxygenase and may be one of the enzymes responsible for polystyrene degradation by the putative Klebsiella oxytoca ATCC 13182 in T. molitor.
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从褐天牛肠道中分离出的克雷伯菌株中 alkB 基因的分子检测和系统发育分析
聚苯乙烯处理面临的挑战促使研究人员急需寻找创新和生态友好的塑料降解解决方案。据报道,一些昆虫将聚苯乙烯作为其唯一的碳源,这与昆虫内脏中存在帮助消化塑料的微生物有关。因此,本研究重点对从褐斑天牛肠道中分离出的氧合克雷伯氏菌菌株中的烷烃-1-单加氧酶(alkB)基因进行分子检测和系统发育分析。alkB 基因编码烷烃-1-单加氧酶,这是一种参与氧化失活烷烃的酶。该基因可用作评估细菌生物降解聚苯乙烯能力的标记。从黄粉虫内脏中分离出三种细菌菌株,并通过 16S 核糖体 RNA 基因的聚合酶链反应(PCR)进行确认。用于扩增 16S 核糖体 RNA 区域的引物是利用生物信息学工具 NCBI 设计的。为检测分离出的细菌菌株中是否存在 alkB 基因,根据 GenBank 中 11 种细菌的 alkB 核苷酸序列的保守区人工设计了一套用于扩增该基因的引物。使用 TCOFFE 在线工具对细菌的 alkB 序列进行比对,并使用 Jalview 和 ConSurf 查看比对结果。然后利用桑格测序技术对扩增的 alkB 基因进行测序,并在 NCBI 上搜索相似序列,构建系统发生树。根据 16S 核糖体 RNA 基因序列,分离出的细菌菌株被确认为产气克雷伯氏菌(Klebsiella oxytoca NBRC 102593)、产气克雷伯氏菌(Klebsiella oxytoca JCM 1665)和产气克雷伯氏菌(Klebsiella oxytoca ATCC 13182)。据我们所知,这是首次在克雷伯菌中检测到与来自放线菌全基因组的 14 个 alkB 基因序列相同的 alkB 基因序列。新的核苷酸序列已发表在 NCBI 数据库中,登录号为 OP959069。该基因序列被认为是烷烃-1-单加氧酶,可能是推测的氧合克雷伯氏菌 ATCC 13182 在褐飞虱体内降解聚苯乙烯的酶之一。
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来源期刊
The Scientific World Journal
The Scientific World Journal 综合性期刊-综合性期刊
CiteScore
5.60
自引率
0.00%
发文量
170
审稿时长
3.7 months
期刊介绍: The Scientific World Journal is a peer-reviewed, Open Access journal that publishes original research, reviews, and clinical studies covering a wide range of subjects in science, technology, and medicine. The journal is divided into 81 subject areas.
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