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真菌中的磷酸盐饥饿会促使磷脂酰胆碱被无磷的甜菜碱脂质二酰甘油-N,N,N-三甲基高丝氨酸所取代。

Phosphate starvation in fungi induces the replacement of phosphatidylcholine with the phosphorus-free betaine lipid diacylglyceryl-N,N,N-trimethylhomoserine.

作者信息

Riekhof Wayne R, Naik Surabhi, Bertrand Helmut, Benning Christoph, Voelker Dennis R

机构信息

Department of Medicine, National Jewish Health, Denver, Colorado, USA School of Biological Sciences, University of Nebraska, Lincoln, Nebraska, USA

School of Biological Sciences, University of Nebraska, Lincoln, Nebraska, USA.

出版信息

Eukaryot Cell. 2014 Jun;13(6):749-57. doi: 10.1128/EC.00004-14. Epub 2014 Apr 11.

Abstract

Diacylglyceryl-N,N,N-trimethylhomoserine (DGTS) is a phosphorus-free betaine-lipid analog of phosphatidylcholine (PtdCho) synthesized by many soil bacteria, algae, and nonvascular plants. Synthesis of DGTS and other phosphorus-free lipids in bacteria occurs in response to phosphorus (P) deprivation and results in the replacement of phospholipids by nonphosphorous lipids. The genes encoding DGTS biosynthetic enzymes have previously been identified and characterized in bacteria and the alga Chlamydomonas reinhardtii. We now report that many fungal genomes, including those of plant and animal pathogens, encode the enzymatic machinery for DGTS biosynthesis, and that fungi synthesize DGTS during P limitation. This finding demonstrates that replacement of phospholipids by nonphosphorous lipids is a strategy used in divergent eukaryotic lineages for the conservation of P under P-limiting conditions. Mutants of Neurospora crassa were used to show that DGTS synthase encoded by the BTA1 gene is solely responsible for DGTS biosynthesis and is under the control of the fungal phosphorus deprivation regulon, mediated by the NUC-1/Pho4p transcription factor. Furthermore, we describe the rational reengineering of lipid metabolism in the yeast Saccharomyces cerevisiae, such that PtdCho is completely replaced by DGTS, and demonstrate that essential processes of membrane biogenesis and organelle assembly are functional and support growth in the engineered strain.

摘要

二酰甘油 - N,N,N - 三甲基高丝氨酸(DGTS)是一种由许多土壤细菌、藻类和非维管植物合成的无磷甜菜碱脂质类似物,其类似于磷脂酰胆碱(PtdCho)。细菌中DGTS和其他无磷脂质的合成是对磷(P)缺乏的响应,导致磷脂被无磷脂质取代。编码DGTS生物合成酶的基因先前已在细菌和莱茵衣藻中得到鉴定和表征。我们现在报告,许多真菌基因组,包括植物和动物病原体的基因组,都编码DGTS生物合成的酶机制,并且真菌在磷限制期间合成DGTS。这一发现表明,在磷限制条件下,用无磷脂质取代磷脂是不同真核生物谱系中用于磷守恒的一种策略。粗糙脉孢菌的突变体被用于表明由BTA1基因编码的DGTS合酶单独负责DGTS的生物合成,并且受真菌磷缺乏调节子的控制,该调节子由NUC - 1/Pho4p转录因子介导。此外,我们描述了酿酒酵母脂质代谢的合理改造,使得PtdCho完全被DGTS取代,并证明膜生物发生和细胞器组装的基本过程是功能性的,并支持工程菌株的生长。

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