Tanaya Behera Himadri, Mojumdar Abhik, Kumari Khushbu, Kumar Gouda Sudhansu, Das Smrutiranjan, Ray Lopamudra
School of Biotechnology, Kalinga Institute of Industrial Technology (KIIT), Deemed to be University, Bhubaneswar, Odisha India.
School of Law, Kalinga Institute of Industrial Technology (KIIT), Deemed to be University, Bhubaneswar, Odisha India.
3 Biotech. 2022 May;12(5):120. doi: 10.1007/s13205-022-03184-5. Epub 2022 Apr 23.
RC1830 was previously isolated as a novel chitinolytic streptomycete from Chilika Lake, Odisha, India. The strain RC1830 is a representative member of the soil-dwelling, filamentous group that produces the majority of natural antibiotics and secondary metabolites. The objective of this work was to assess the chitin degradation ability and whole-genome sequence of RC1830. TLC analysis of the fermentation product revealed that strain RC1830 can convert shrimp shell colloidal chitin to -acetylated chitooligosaccharides (-AcCOS). A genome-wide investigation of RC1830 was also carried out to investigate the genetic basis for chitin breakdown. The result showed that the RC1830 genome possesses a chromosome with 7,121,774 bp (73.2% GC). The genome consists of 6807 coding sequences, 69 tRNA, and 3 rRNA genes. Furthermore, carbohydrate-active enzyme (CAZyme) analysis revealed that RC1830 has 89 glycoside hydrolase family genes, which could modulate the enzymes involved in the degradation of chitin ultimately producing industrially important COS. The whole-genome information of RC1830 could emphasize the mechanism involved in the RC1830's chitin breakdown activity, endowing RC1830 with a promising alternative for COS production.
The online version contains supplementary material available at 10.1007/s13205-022-03184-5.
RC1830先前是从印度奥里萨邦奇利卡湖分离出的一种新型几丁质分解链霉菌。菌株RC1830是土壤栖息丝状菌群的代表性成员,该菌群产生了大部分天然抗生素和次级代谢产物。这项工作的目的是评估RC1830的几丁质降解能力和全基因组序列。发酵产物的薄层色谱分析表明,菌株RC1830可将虾壳胶体几丁质转化为N-乙酰化壳寡糖(N-AcCOS)。还对RC1830进行了全基因组研究,以探究几丁质分解的遗传基础。结果表明,RC1830基因组拥有一条7,121,774 bp(GC含量73.2%)的染色体。该基因组由6807个编码序列、69个tRNA和3个rRNA基因组成。此外,碳水化合物活性酶(CAZyme)分析表明,RC1830有89个糖苷水解酶家族基因,这些基因可调节参与几丁质降解的酶,最终产生具有工业重要性的壳寡糖。RC1830的全基因组信息可强化RC1830几丁质分解活性所涉及的机制,使RC1830成为壳寡糖生产的一个有前景的替代方案。
在线版本包含可在10.1007/s13205-022-03184-5获取的补充材料。