Bagar Tanja, Altenbach Kirsten, Read Nick D, Bencina Mojca
Department of Biotechnology, National Institute of Chemistry, Ljubljana, Slovenia.
Eukaryot Cell. 2009 May;8(5):703-12. doi: 10.1128/EC.00333-08. Epub 2009 Mar 13.
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.
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。