• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

酵母毕赤酵母的亚细胞蛋白质组图谱。

A subcellular proteome atlas of the yeast Komagataella phaffii.

机构信息

Austrian Centre of Industrial Biotechnology (ACIB), Muthgasse 11, 1190 Vienna, Austria.

Department of Biotechnology, BOKU-University of Natural Resources and Life Sciences, Muthgasse 18, 1190 Vienna, Austria.

出版信息

FEMS Yeast Res. 2020 Feb 1;20(1). doi: 10.1093/femsyr/foaa001.

DOI:10.1093/femsyr/foaa001
PMID:31922548
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6981350/
Abstract

The compartmentalization of metabolic and regulatory pathways is a common pattern of living organisms. Eukaryotic cells are subdivided into several organelles enclosed by lipid membranes. Organelle proteomes define their functions. Yeasts, as simple eukaryotic single cell organisms, are valuable models for higher eukaryotes and frequently used for biotechnological applications. While the subcellular distribution of proteins is well studied in Saccharomyces cerevisiae, this is not the case for other yeasts like Komagataella phaffii (syn. Pichia pastoris). Different to most well-studied yeasts, K. phaffii can grow on methanol, which provides specific features for production of heterologous proteins and as a model for peroxisome biology. We isolated microsomes, very early Golgi, early Golgi, plasma membrane, vacuole, cytosol, peroxisomes and mitochondria of K. phaffii from glucose- and methanol-grown cultures, quantified their proteomes by liquid chromatography-electrospray ionization-mass spectrometry of either unlabeled or tandem mass tag-labeled samples. Classification of the proteins by their relative enrichment, allowed the separation of enriched proteins from potential contaminants in all cellular compartments except the peroxisomes. We discuss differences to S. cerevisiae, outline organelle specific findings and the major metabolic pathways and provide an interactive map of the subcellular localization of proteins in K. phaffii.

摘要

代谢和调控途径的区室化是生物的普遍模式。真核细胞被划分为几个由脂膜包裹的细胞器。细胞器蛋白质组定义了它们的功能。酵母作为简单的真核单细胞生物,是高等真核生物的有价值模型,并且经常用于生物技术应用。虽然在酿酒酵母中对蛋白质的亚细胞分布进行了很好的研究,但 Komagataella phaffii(又名 Pichia pastoris)等其他酵母则并非如此。与大多数研究充分的酵母不同,K. phaffii 可以在甲醇上生长,这为异源蛋白质的生产提供了特定的特征,并作为过氧化物酶体生物学的模型。我们从葡萄糖和甲醇培养的 K. phaffii 中分离出微粒体、早期高尔基器、早期高尔基器、质膜、液泡、细胞质、过氧化物酶体和线粒体,通过未标记或串联质量标签标记样品的液相色谱-电喷雾电离-质谱法对它们的蛋白质组进行定量。通过相对丰度对蛋白质进行分类,允许除过氧化物酶体外的所有细胞区室中的浓缩蛋白质与潜在污染物分离。我们讨论了与酿酒酵母的差异,概述了细胞器特异性发现以及主要代谢途径,并提供了 K. phaffii 中蛋白质亚细胞定位的交互式图谱。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0b43/6981350/0b3c87859a35/foaa001fig8.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0b43/6981350/a34647938a68/foaa001fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0b43/6981350/276006978786/foaa001fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0b43/6981350/072e77235d63/foaa001fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0b43/6981350/bed4fb62ede9/foaa001fig4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0b43/6981350/a3c60434f174/foaa001fig5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0b43/6981350/7714ea3d9a32/foaa001fig6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0b43/6981350/415f1f49d0f8/foaa001fig7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0b43/6981350/0b3c87859a35/foaa001fig8.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0b43/6981350/a34647938a68/foaa001fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0b43/6981350/276006978786/foaa001fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0b43/6981350/072e77235d63/foaa001fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0b43/6981350/bed4fb62ede9/foaa001fig4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0b43/6981350/a3c60434f174/foaa001fig5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0b43/6981350/7714ea3d9a32/foaa001fig6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0b43/6981350/415f1f49d0f8/foaa001fig7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0b43/6981350/0b3c87859a35/foaa001fig8.jpg

相似文献

1
A subcellular proteome atlas of the yeast Komagataella phaffii.酵母毕赤酵母的亚细胞蛋白质组图谱。
FEMS Yeast Res. 2020 Feb 1;20(1). doi: 10.1093/femsyr/foaa001.
2
What makes Komagataella phaffii non-conventional?是什么让糠秕假丝酵母具有非常规性?
FEMS Yeast Res. 2021 Dec 24;21(8). doi: 10.1093/femsyr/foab059.
3
Microbe Profile: : a methanol devouring biotech yeast formerly known as .微生物简介:一种甲醇吞噬生物科技酵母,原名 。
Microbiology (Reading). 2020 Jul;166(7):614-616. doi: 10.1099/mic.0.000958.
4
Carbon source requirements for mating and mating-type switching in the methylotrophic yeasts Ogataea (Hansenula) polymorpha and Komagataella phaffii (Pichia pastoris).甲醇营养型酵母 Ogataea (Hansenula) polymorpha 和 Komagataella phaffii (毕赤酵母) 的交配和交配型转换的碳源需求。
Yeast. 2020 Feb;37(2):237-245. doi: 10.1002/yea.3446. Epub 2020 Jan 6.
5
Impact of Oxygen Availability on the Organelle-Specific Redox Potentials and Stress in Recombinant Protein Producing Komagataella phaffii.氧气可用性对产重组蛋白的毕赤酵母细胞器特异性氧化还原电位和应激的影响。
Microb Biotechnol. 2025 Feb;18(2):e70106. doi: 10.1111/1751-7915.70106.
6
() as a Powerful Yeast Expression System for Biologics Production.()作为用于生物制品生产的强大酵母表达系统。
Front Biosci (Elite Ed). 2024 Jun 12;16(2):19. doi: 10.31083/j.fbe1602019.
7
Two homologs of the Cat8 transcription factor are involved in the regulation of ethanol utilization in Komagataella phaffii.Cat8 转录因子的两个同源物参与调控毕赤酵母乙醇利用。
Curr Genet. 2021 Aug;67(4):641-661. doi: 10.1007/s00294-021-01165-4. Epub 2021 Mar 16.
8
as Emerging Model Organism in Fundamental Research.作为基础研究中的新兴模式生物。
Front Microbiol. 2021 Jan 11;11:607028. doi: 10.3389/fmicb.2020.607028. eCollection 2020.
9
Enhancing xylanase expression by Komagataella phaffii by formate as carbon source and inducer.通过甲酸盐作为碳源和诱导剂来增强毕赤酵母中木聚糖酶的表达。
Appl Microbiol Biotechnol. 2022 Dec;106(23):7819-7829. doi: 10.1007/s00253-022-12249-7. Epub 2022 Oct 29.
10
Knock-out of the major regulator Flo8 in Komagataella phaffii results in unique host strain performance for methanol-free recombinant protein production.在毕赤酵母中敲除主要调控因子Flo8会产生用于无甲醇重组蛋白生产的独特宿主菌株性能。
N Biotechnol. 2024 Dec 25;84:105-114. doi: 10.1016/j.nbt.2024.10.001. Epub 2024 Oct 9.

引用本文的文献

1
Impact of Oxygen Availability on the Organelle-Specific Redox Potentials and Stress in Recombinant Protein Producing Komagataella phaffii.氧气可用性对产重组蛋白的毕赤酵母细胞器特异性氧化还原电位和应激的影响。
Microb Biotechnol. 2025 Feb;18(2):e70106. doi: 10.1111/1751-7915.70106.
2
CRISPR-Cas9 knockout screen informs efficient reduction of the Komagataella phaffii secretome.CRISPR-Cas9基因敲除筛选有助于有效减少毕赤酵母分泌组。
Microb Cell Fact. 2024 Jul 31;23(1):217. doi: 10.1186/s12934-024-02466-2.
3
Characterising the metabolic rewiring of extremely slow growing Komagataella phaffii.

本文引用的文献

1
A consensus S. cerevisiae metabolic model Yeast8 and its ecosystem for comprehensively probing cellular metabolism.共识 S. cerevisiae 代谢模型 Yeast8 及其生态系统,用于全面探究细胞代谢。
Nat Commun. 2019 Aug 8;10(1):3586. doi: 10.1038/s41467-019-11581-3.
2
The subcellular organisation of Saccharomyces cerevisiae.酿酒酵母的亚细胞结构组织。
Curr Opin Chem Biol. 2019 Feb;48:86-95. doi: 10.1016/j.cbpa.2018.10.026. Epub 2018 Nov 29.
3
Tempo and Mode of Genome Evolution in the Budding Yeast Subphylum.出芽酵母亚界的基因组进化时空调控与模式。
描绘极度缓慢生长的 Komagataella phaffii 的代谢重排。
Microb Biotechnol. 2024 Jan;17(1):e14386. doi: 10.1111/1751-7915.14386. Epub 2024 Jan 11.
4
Alternative PCR-Based Approaches for Generation of Strains.基于聚合酶链式反应的菌株构建替代方法。
Microorganisms. 2023 Sep 12;11(9):2297. doi: 10.3390/microorganisms11092297.
5
Genome-scale modeling of yeast metabolism: retrospectives and perspectives.酵母代谢的基因组规模建模:回顾与展望。
FEMS Yeast Res. 2022 Feb 22;22(1). doi: 10.1093/femsyr/foac003.
6
Subcellular Transcriptomics and Proteomics: A Comparative Methods Review.亚细胞转录组学和蛋白质组学:比较方法综述。
Mol Cell Proteomics. 2022 Feb;21(2):100186. doi: 10.1016/j.mcpro.2021.100186. Epub 2021 Dec 16.
7
What makes Komagataella phaffii non-conventional?是什么让糠秕假丝酵母具有非常规性?
FEMS Yeast Res. 2021 Dec 24;21(8). doi: 10.1093/femsyr/foab059.
8
Beyond alcohol oxidase: the methylotrophic yeast Komagataella phaffii utilizes methanol also with its native alcohol dehydrogenase Adh2.超越酒精氧化酶:甲醇营养型酵母毕赤酵母 Komagataella phaffii 也利用其天然的醇脱氢酶 Adh2 来利用甲醇。
FEMS Yeast Res. 2021 Mar 18;21(2). doi: 10.1093/femsyr/foab009.
9
as Emerging Model Organism in Fundamental Research.作为基础研究中的新兴模式生物。
Front Microbiol. 2021 Jan 11;11:607028. doi: 10.3389/fmicb.2020.607028. eCollection 2020.
10
Harnessing sub-organelle metabolism for biosynthesis of isoprenoids in yeast.利用亚细胞器代谢在酵母中进行类异戊二烯的生物合成。
Synth Syst Biotechnol. 2020 Jul 1;5(3):179-186. doi: 10.1016/j.synbio.2020.06.005. eCollection 2020 Sep.
Cell. 2018 Nov 29;175(6):1533-1545.e20. doi: 10.1016/j.cell.2018.10.023. Epub 2018 Nov 8.
4
Metabolic engineering of Pichia pastoris.毕赤酵母的代谢工程。
Metab Eng. 2018 Nov;50:2-15. doi: 10.1016/j.ymben.2018.04.017. Epub 2018 Apr 25.
5
Fine-tuning the P. pastoris iMT1026 genome-scale metabolic model for improved prediction of growth on methanol or glycerol as sole carbon sources.优化毕赤酵母 iMT1026 基因组尺度代谢模型,提高甲醇或甘油作为唯一碳源时的生长预测能力。
Microb Biotechnol. 2018 Jan;11(1):224-237. doi: 10.1111/1751-7915.12871. Epub 2017 Nov 21.
6
Experimental Systems to Study Yeast Pexophagy.用于研究酵母细胞自噬的实验系统
Methods Mol Biol. 2017;1595:249-255. doi: 10.1007/978-1-4939-6937-1_24.
7
Assays to Monitor Pexophagy in Yeast.监测酵母中pexophagy的实验方法。
Methods Enzymol. 2017;588:413-427. doi: 10.1016/bs.mie.2016.09.088. Epub 2016 Nov 30.
8
Disruption of genes involved in CORVET complex leads to enhanced secretion of heterologous carboxylesterase only in protease deficient Pichia pastoris.参与CORVET复合体的基因的破坏仅在蛋白酶缺陷型毕赤酵母中导致异源羧酸酯酶分泌增加。
Biotechnol J. 2017 May;12(5). doi: 10.1002/biot.201600584. Epub 2017 Mar 30.
9
Curation of the genome annotation of Pichia pastoris (Komagataella phaffii) CBS7435 from gene level to protein function.从基因水平到蛋白质功能对毕赤酵母(Komagataella phaffii)CBS7435的基因组注释进行整理。
FEMS Yeast Res. 2016 Sep;16(6). doi: 10.1093/femsyr/fow051. Epub 2016 Jul 6.
10
The Emerging Network of Mitochondria-Organelle Contacts.线粒体-细胞器接触的新兴网络
Mol Cell. 2016 Mar 3;61(5):648-653. doi: 10.1016/j.molcel.2016.01.031.