Pal Srikanta, Biswas Raju, Sar Abhijit, Misra Arijit, Dam Somasri, Dam Bomba
Microbiology Laboratory, Department of Botany (DST-FIST and UGC-DRS Funded), Institute of Science, Visva-Bharati (A Central University), Santiniketan, West Bengal, 731235, India.
Techno India University, Kolkata, West Bengal, India.
Extremophiles. 2025 Jan 28;29(1):14. doi: 10.1007/s00792-025-01378-2.
To fish-out novel salt-tolerance genes, metagenomic DNA of moderately saline sediments of India's largest hypersaline Sambhar Lake was cloned in fosmid. Two functionally-picked clones helped the Escherichia coli host to tolerate 0.6 M NaCl. Deep sequencing of their fosmid DNA insert revealed 32-37% of genes to encode transporters, mostly belonging to ABC (ATP-Binding Cassette)-type, but none specific to channel Na. The complete metagenome sequence of Sambhar Lake brines, and reanalysed data of twelve other hypersaline metagenome sequences, however, have only around 5% transporter genes, suggesting metagenomic DNA fragments being biasedly-cloned during functional screening. Almost half of the ~ 40 Kb inserts in the two clones was shared, and encode several transporters, and some transposase. This advocates that these transporter-loaded DNA lengths are shuttled among microorganisms of hypersaline environments. Interestingly, one clone showed retarded growth with prominent cell disruptions in scanning electron microscopic images, when fosmid copy number was increased or transporters were NaCl-induced. Its cloned insert exclusively has three genes, encoding a structurally functional ATP-binding protein and its efflux component, whose possible overexpression led to membrane crowding and cell rupture. Thus, microorganisms thriving in hypersaline lakes have plentiful ABC transporters that are mutually shared among themselves. These novel salt tolerance genes have future agricultural biotechnological potential.
为了筛选出新型耐盐基因,将印度最大的超盐湖桑巴尔湖中度盐渍沉积物的宏基因组DNA克隆到fosmid载体中。两个经过功能筛选的克隆使大肠杆菌宿主能够耐受0.6M NaCl。对其fosmid DNA插入片段进行深度测序发现,32%-37%的基因编码转运蛋白,其中大部分属于ABC(ATP结合盒)型,但没有特定的钠通道基因。然而,桑巴尔湖卤水的完整宏基因组序列以及对其他12个超盐宏基因组序列重新分析的数据显示,只有约5%的转运蛋白基因,这表明在功能筛选过程中宏基因组DNA片段被偏向性克隆。两个克隆中约40Kb的插入片段几乎有一半是相同的,它们编码几种转运蛋白和一些转座酶。这表明这些携带转运蛋白的DNA片段在超盐环境的微生物之间穿梭。有趣的是,当fosmid拷贝数增加或转运蛋白被NaCl诱导时,一个克隆在扫描电子显微镜图像中显示生长迟缓且细胞有明显破坏。其克隆插入片段仅含有三个基因,编码一种具有结构功能的ATP结合蛋白及其外排成分,其可能的过表达导致膜拥挤和细胞破裂。因此,在超盐湖中繁衍生息的微生物拥有丰富的ABC转运蛋白,它们在彼此之间相互共享。这些新型耐盐基因具有未来农业生物技术潜力。