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DOI | 10.3389/fchem.2020.00197 |
Potashchelins, a Suite of Lipid Siderophores Bearing Both L-threo and L-erythro Beta-Hydroxyaspartic Acids, Acquired From the Potash-Salt-Ore-Derived Extremophile Halomonas sp. MG34 | |
Li, Yihong; Liu, Li; Zhang, Gengxin; He, Ning; Guo, Wenqiang; Hong, Bin; Xie, Yunying | |
通讯作者 | Hong, B ; Xie, YY (通讯作者) |
发表日期 | 2020 |
ISSN | 2296-2646 |
卷号 | 8 |
英文摘要 | Four new lipid siderophores bearing both L-threo- and L-erythro-beta-hydroxyaspartic acids, potashchelins A-D (1-4), were isolated from the potash-salt-ore-derived extremophile Halomonas sp. MG34. The planar structures of 1-4 were elucidated on the basis of extensive 1D and 2D NMR studies and MS/MS data. Potashchelins 1-4 contain a hydrophilic nonapeptide headgroup sequentially consisting of beta-hydroxyaspartic acid, serine, glycine, serine, serine, beta-hydroxyaspartic acid, threonine, serine, and cyclic N(delta)-hydroxy-ornithine, which is appended by one of a series of fatty acids ranging from dodecanoic acid to tetradecanoic acid. The absolute configurations of the amino acids of potashchelins 1-4 were determined by C-3 and advanced Marfey's reaction, partial hydrolysis, and bioinformatics analysis, which revealed that potashchelins 1-4 bear both L-threo- and L-erythro-beta-hydroxyaspartic acid. Phylogenetic analysis showed that the stand-alone beta-hydroxylase, PtcA, and the fused domain with beta-hydroxylase activity in PtcB are expected to be responsible for the formation of L-erythro and L-threo diastereomers, respectively. Additionally, utilizing a comparative genomics approach, we revealed an evolutionary mechanism for lipid siderophores in Halomonas involving horizontal transfer. Bioassays showed that potashchelin A and D had weak antibacterial activity against B. subtilis CPCC 100029 with an MIC value of 64 mu g/mL. |
关键词 | GENOMICS-DRIVEN DISCOVERYCONSTITUENT AMINO-ACIDSAMPHIPHILIC SIDEROPHORESSTRUCTURAL-CHARACTERIZATIONABSOLUTE-CONFIGURATIONMARFEYS METHODBIOSYNTHESISSYRINGOMYCINDOMAINLC/MS |
英文关键词 | potashchelins; lipid siderophore; L-threo-beta-hydroxyaspartic acid; L-erythro-beta-hydroxyaspartic acid; Halomonas; beta-hydroxylases |
语种 | 英语 |
WOS研究方向 | Chemistry |
WOS类目 | Chemistry, Multidisciplinary |
WOS记录号 | WOS:000523446800001 |
来源期刊 | FRONTIERS IN CHEMISTRY |
来源机构 | 中国科学院青藏高原研究所 |
文献类型 | 期刊论文 |
条目标识符 | http://gcip.llas.ac.cn/handle/2XKMVOVA/259750 |
推荐引用方式 GB/T 7714 | Li, Yihong,Liu, Li,Zhang, Gengxin,et al. Potashchelins, a Suite of Lipid Siderophores Bearing Both L-threo and L-erythro Beta-Hydroxyaspartic Acids, Acquired From the Potash-Salt-Ore-Derived Extremophile Halomonas sp. MG34[J]. 中国科学院青藏高原研究所,2020,8. |
APA | Li, Yihong.,Liu, Li.,Zhang, Gengxin.,He, Ning.,Guo, Wenqiang.,...&Xie, Yunying.(2020).Potashchelins, a Suite of Lipid Siderophores Bearing Both L-threo and L-erythro Beta-Hydroxyaspartic Acids, Acquired From the Potash-Salt-Ore-Derived Extremophile Halomonas sp. MG34.FRONTIERS IN CHEMISTRY,8. |
MLA | Li, Yihong,et al."Potashchelins, a Suite of Lipid Siderophores Bearing Both L-threo and L-erythro Beta-Hydroxyaspartic Acids, Acquired From the Potash-Salt-Ore-Derived Extremophile Halomonas sp. MG34".FRONTIERS IN CHEMISTRY 8(2020). |
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