制备萜烯的酿酒酵母对己糖激酶ii耗竭的蛋白质组学反应分析

Zeyu Lu , Qianyi Shen , Lian Liu , Gert Talbo , Robert Speight , Matt Trau , Geoff Dumsday , Christopher B. Howard , Claudia E. Vickers , Bingyin Peng
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引用次数: 1

摘要

己糖激酶II (Hxk2)是葡萄糖介导的转录抑制信号通路中的主蛋白。通过生长素诱导的蛋白质降解Hxk2,以前在酿酒酵母中以克/升的水平加倍倍半萜(神经醇)的产量。hxk2缺失背景下的全局转录组学/蛋白质组学分析对于理解神经醇生成的遗传和分子机制以及指导进一步的菌株优化具有重要意义。本文研究了在指数和乙醇生长阶段以及gal80野生型和gal80Δ背景下,含有GAL启动子控制的神经醇合成途径的酵母菌株对Hxk2缺失的蛋白质组学响应。碳代谢途径和氨基酸代谢途径对Hxk2的消耗和乙醇的生长表现出多样化的响应,包括替代碳分解代谢和呼吸的上调以及氨基酸合成的下调。去抑制GAL基因可能有助于提高hxk2缺失菌株的神经醇产量。17个与上调基因相关的转录因子被富集。验证Ash1介导的RIM4启动子上的抑制显示了不同Ash1结合位点的调节作用的差异以及Ash1和hxk2介导的抑制的协同作用。对单个启动子的进一步验证表明,在hxk2Δ背景下,HXT1启动子的活性是葡萄糖依赖性的,但比hxk2野生型背景弱得多。综上所述,灭活HXK2可能减轻葡萄糖对酿酒酵母呼吸和GAL启动子的抑制,从而改善好氧条件下的生物生产。蛋白质组学图谱为hxk2缺乏背景下更好的代谢工程设计提供了更好的遗传学概述。
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Profiling proteomic responses to hexokinase-II depletion in terpene-producing Saccharomyces cerevisiae

Hexokinase II (Hxk2) is a master protein in glucose-mediated transcriptional repression signaling pathway. Degrading Hxk2 through an auxin-inducible protein degradation previously doubled sesquiterpene (nerolidol) production at gram-per-liter levels in Saccharomyces cerevisiae. Global transcriptomics/proteomics profiles in Hxk2-deficient background are important to understanding genetic and molecular mechanisms for improved nerolidol production and guiding further strain optimization. Here, proteomic responses to Hxk2 depletion are investigated in the yeast strains harboring a GAL promoters-controlled nerolidol synthetic pathway, at the exponential and ethanol growth phases and in GAL80-wildtype and gal80Δ backgrounds. Carbon metabolic pathways and amino acid metabolic pathways show diversified responses to Hxk2 depletion and growth on ethanol, including upregulation of alternative carbon catabolism and respiration as well as downregulation of amino acid synthesis. De-repression of GAL genes may contribute to improved nerolidol production in Hxk2-depleted strains. Seventeen transcription factors associated with upregulated genes are enriched. Validating Ash1-mediated repression on the RIM4 promoter shows the variation on the regulatory effects of different Ash1-binding sites and the synergistic effect of Ash1 and Hxk2-mediated repression. Further validation of individual promoters shows that HXT1 promoter activities are glucose-dependent in hxk2Δ background, but much weaker than those in HXK2-wildtype background. In summary, inactivating HXK2 may relieve glucose repression on respiration and GAL promoters for improved bioproduction under aerobic conditions in S. cerevisiae. The proteomics profiles provide a better genetics overview for a better metabolic engineering design in Hxk2-deficient backgrounds.

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