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A comparative genomic analysis of calcium and proton signaling/homeostasis in Aspergillus species.曲霉菌种中钙和质子信号传导/内稳态的比较基因组分析。
Fungal Genet Biol. 2009 Mar;46 Suppl 1:S93-S104. doi: 10.1016/j.fgb.2008.07.019.
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Imaging living cells of Aspergillus in vitro.体外成像烟曲霉的活细胞。
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Vacuolar and plasma membrane proton pumps collaborate to achieve cytosolic pH homeostasis in yeast.液泡膜质子泵和质膜质子泵协同作用,以实现酵母细胞溶质pH稳态。
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High-precision FLIM-FRET in fixed and living cells reveals heterogeneity in a simple CFP-YFP fusion protein.在固定细胞和活细胞中进行的高精度荧光寿命成像-荧光共振能量转移(FLIM-FRET)揭示了一种简单的CFP-YFP融合蛋白中的异质性。
Biophys Chem. 2007 May;127(3):155-64. doi: 10.1016/j.bpc.2007.01.008. Epub 2007 Feb 1.
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Genome sequencing and analysis of the versatile cell factory Aspergillus niger CBS 513.88.多功能细胞工厂黑曲霉CBS 513.88的基因组测序与分析
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Changes in primary metabolism leading to citric acid overflow in Aspergillus niger.黑曲霉中导致柠檬酸溢流的初级代谢变化。
Biotechnol Lett. 2007 Feb;29(2):181-90. doi: 10.1007/s10529-006-9235-z. Epub 2006 Nov 22.
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Metabolic regulation of neutrophil spreading, membrane tubulovesicular extensions (cytonemes) formation and intracellular pH upon adhesion to fibronectin.中性粒细胞在黏附于纤连蛋白时的铺展、膜微管泡状延伸(丝状伪足)形成及细胞内pH的代谢调控。
Exp Cell Res. 2006 Aug 1;312(13):2568-79. doi: 10.1016/j.yexcr.2006.04.011. Epub 2006 May 3.
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A novel fluorescent pH probe for expression in plants.一种用于植物表达的新型荧光 pH 探针。
Plant Methods. 2006 Apr 6;2:7. doi: 10.1186/1746-4811-2-7.
9
PixFRET, an ImageJ plug-in for FRET calculation that can accommodate variations in spectral bleed-throughs.PixFRET,一款用于FRET计算的ImageJ插件,可适应光谱渗漏的变化。
Microsc Res Tech. 2005 Sep;68(1):51-8. doi: 10.1002/jemt.20215.
10
Influence of dissolved oxygen concentration on intracellular pH for regulation of Aspergillus niger growth rate during citric acid fermentation in a stirred tank bioreactor.搅拌罐式生物反应器中柠檬酸发酵过程中溶解氧浓度对黑曲霉生长速率调节时细胞内pH值的影响。
Int J Biol Sci. 2005;1(1):34-41. Epub 2005 Feb 5.

使用基因编码的比率探针进行丝状真菌活细胞成像及细胞内pH值测量。

Live-Cell imaging and measurement of intracellular pH in filamentous fungi using a genetically encoded ratiometric probe.

作者信息

Bagar Tanja, Altenbach Kirsten, Read Nick D, Bencina Mojca

机构信息

Department of Biotechnology, National Institute of Chemistry, Ljubljana, Slovenia.

出版信息

Eukaryot Cell. 2009 May;8(5):703-12. doi: 10.1128/EC.00333-08. Epub 2009 Mar 13.

DOI:10.1128/EC.00333-08
PMID:19286983
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2681602/
Abstract

A novel, genetically encoded, ratiometric pH probe (RaVC) was constructed to image and measure intracellular pH in living hyphae of Aspergillus niger. RaVC is a chimeric protein based on the pH-sensitive probe pHluorin, which was partially codon optimized for expression in Aspergillus. Intracellular pH imaging and measurement was performed by simultaneous, dual-excitation confocal ratio imaging. The mean cytoplasmic pH measured was 7.4 to 7.7 based on calibrating RaVC in situ within nigericin-treated hyphae. Pronounced, longitudinal cytoplasmic pH gradients were not observed in the apical 20 microm of actively growing hyphae at the periphery of 18-h-old colonies. The cytoplasmic pH remained unchanged after prolonged growth in buffered medium with pH values between 2.5 or 9.5. Sudden changes in external pH significantly changed cytoplasmic pH by <1.3 pH units, but it returned to its original value within 20 min following treatment. The weak acid and antifungal food preservative sorbic acid caused prolonged, concentration-dependent intracellular acidification. The inhibition of ATPases with N-ethylmaleimide, dicychlohexylcarbodimide, or sodium azide caused the cytoplasmic pH to decrease by <1 pH unit. Treatment with the protonophore carbonyl cyanide m-chlorophenylhydrazone or cyanide p-(trifluoromethoxy) phenylhydrazone reduced the cytoplasmic pH by <1 pH unit. In older hyphae from 32-h-old cultures, RaVC became sequestered within large vacuoles, which were shown to have pH values between 6.2 and 6.5. Overall, our study demonstrates that RaVC is an excellent probe for visualizing and quantifying intracellular pH in living fungal hyphae.

摘要

构建了一种新型的、基因编码的比率型pH探针(RaVC),用于对黑曲霉活菌丝中的细胞内pH进行成像和测量。RaVC是一种基于pH敏感探针pHluorin的嵌合蛋白,该探针针对在曲霉中的表达进行了部分密码子优化。通过同步双激发共聚焦比率成像进行细胞内pH成像和测量。基于在尼日利亚菌素处理的菌丝中原位校准RaVC,测得的平均细胞质pH为7.4至7.7。在18小时龄菌落周边活跃生长的菌丝顶端20微米内,未观察到明显的纵向细胞质pH梯度。在pH值为2.5或9.5的缓冲培养基中长时间生长后,细胞质pH保持不变。外部pH的突然变化使细胞质pH显著变化<1.3个pH单位,但在处理后20分钟内恢复到其原始值。弱酸和抗真菌食品防腐剂山梨酸导致长时间的、浓度依赖性的细胞内酸化。用N-乙基马来酰亚胺、二环己基碳二亚胺或叠氮化钠抑制ATP酶导致细胞质pH降低<1个pH单位。用质子载体羰基氰化物间氯苯腙或氰化物对-(三氟甲氧基)苯腙处理使细胞质pH降低<1个pH单位。在32小时龄培养物的老龄菌丝中,RaVC被隔离在大液泡中,这些液泡的pH值在6.2至6.5之间。总体而言,我们的研究表明RaVC是用于可视化和定量活真菌菌丝中细胞内pH的优秀探针。