Study on a Nile Red fluorescence spectrometry for rapid lipid determination in Yarrowia lipolytica
-
摘要: 为了建立快速简便检测解脂耶氏酵母油脂含量的方法,探讨了尼罗红-光谱法测定解脂耶氏酵母油脂含量的检测条件。通过研究解脂耶氏酵母最佳发射光波长、细胞密度、尼罗红染液用量、染色时间、不同助溶剂效能及最佳体积分数对荧光强度的影响,确定了最佳检测条件,得到细胞油脂含量与荧光强度的线性关系。解脂耶氏酵母在激发光560 nm、发射光650 nm处有最高荧光值,每毫升菌液加入质量分数为0.1 mg/m L的尼罗红染液20μL,加入体积分数为15%的异丙醇,黑暗染色5 min,在细胞OD600=01.3的范围内,菌液的油脂含量(X)与荧光值(Y)呈较好的线性关系,线性关系式为Y=6.3651X+10.097,R2=0.9902,灵敏度达0.0001 g。该方法能够准确地反映出解脂耶氏酵母胞内油脂含量。尼罗红-荧光法可成为一种快速检测解脂耶氏酵母胞内油脂含量的新方法。Abstract: In order to establish a rapid lipid determination method in Yarrowia lipolytica, the determination conditions were studied with the Nile Red fluorescence spectrometry. The optimal determination conditions were confirmed by researching the optimal emission wavelength in Yarrowia lipolytica, optimal volume fraction, dosage of Nile Red dye solution, dyeing time and efficiency of different penetrating agents, the linearity between lipid content in cell and fluorescence intensity were affirmed.Yarrowia lipolytica had maximum fluorescence value in excitation wavelength 560 nm, emission wavelength 650 nm, 20 μL0.1 mg/m L mass fraction of Nile Red dye solution and 15% volume fraction of isopropanol were added in per milliliter of Yarrowia lipolytica suspension respectively, dyeing time 5 min in darkness, in the range of cell with OD600 of 01.3, there was a good linear relationship between lipid content ( X) of solution and fluorescence intensity ( Y) , and the linear formula was Y =6.3651 X + 10.097 ( R2= 0.9902) , the sensitivity of this method was 0.0001 g. The Nile Red fluorescence spectrometry could reflect the lipid content accurately in Yarrowia lipolytica and be used as a new method for rapid lipid determination in Yarrowia lipolytica.
-
Keywords:
- Yarrowia lipolytica /
- lipid content /
- Nile Red /
- fluorescence spectrometry
-
[1] Ratledge C, Wynn JP.The biochemistry and molecular biology of lipid accumulation in oleaginous microorganisms[J].Advances in Applied Microbiology, 2002, 51 (1-44) :1-51.
[2] Papanikolaou S, Komaitis M, Aggelis G.Single cell oil (SCO) production by Mortierella isabellina grown on high-sugar content media[J].Bioresource Technology, 2004, 95 (3) :287-291.
[3] Ryckebosch E, Muylaert K, Foubert I, et al.Optimization of an analytical procedure for extraction of lipids from microalgae[J].Journal of the American Oil Chemists’Society, 2012, 89:189-198.
[4] Tai M, Stephanopoulos G.Engineering the push and pull of lipid biosynthesis in oleaginous yeast Yarrowia lipolytica for biofuel production[J].Metabolic Engineering, 2013, 15:1-9.
[5] Abghari A, Chen S.Yarrowia lipolytica as an oleaginous cell factory platform for production of fatty acid-based biofuel and bioproducts[J].Frontiers in Energy Research, 2014, 2:1-21.
[6] Xie DM, Jackson EN, Zhu Q.Sustainable source of omega-3eicosapentaenoic acid from metabolically engineered Yarrowia lipolytica:from fundamental research to commercial production[J].Applied Microbiology and Biotechnology, 2015, 99:1599-1610.
[7] Groenewald M, Boekhout T, Neuvéglise C, et al.Yarrowia lipolytica:safety assessment of an oleaginous yeast with a great industrial potential[J].Critical Reviews in Microbiology, 2014, 40 (3) :187-206.
[8] Bligh EG, Dyer WJ.A rapid method for total lipid extraction and purification[J].Canadian Journal of Biochemistry and Physiology, 1959, 37 (8) :911-917.
[9] 苏晓燕, 张海芳, 姜思远, 等.索氏提取法和酸水解法比较测定午餐肉中脂肪含量[J].黑龙江畜牧兽医, 2016 (19) :289-290. [10] Katariina N, Jukka S, Dagmar S, et al.Nile Red staining of phytoplankton neutral lipids:species-specific fluorescence kinetics in various solvents[J].Journal of Applied Phycology, 2015, 27:1161-1168.
[11] Sitepu IR, Ignatia L, Franz AK, et al.An improved highthroughput Nile red fluorescence assay for estimating intracellular lipids in a variety of yeast species[J].Journal of Microbiological Methods, 2012, 91 (2) :321-328.
[12] Kimura K, Yamaoka M, Kamisaka Y.Rapid estimation of lipids in oleaginous fungi and yeasts using Nile red fluorescence[J].Journal of Microbiological Methods, 2004, 56 (3) :331-338.
[13] Bertozzini E, Galluzzi L, Penna A, et al.Application of the standard addition method for the absolute quantification of neutral lipids in microalgae using Nile red[J].Journal of Microbiological Methods, 2011, 87 (1) :17-23.
[14] 李艾, 郝玉翠, 郝斌, 等.微生物胞内油脂染色法检测技术进展[J].食品工业科技, 2014, 19 (35) :373-377. [15] Chen W, Zhang C, Song L, et al.A high throughput Nile red method for quantitative measurement of neutral lipids in microalgae[J].Journal of Microbiological Methods, 2009, 77 (1) :41-47.
[16] Joseph R, Lakowicz.Principles of Fluorescence Spectroscopy[M].New York, Springer, 2006.
[17] Pick U, Rachutin-Zalogin T.Kinetic anomalies in the interactions of Nile red with microalgae[J].Journal of Microbiological Methods, 2011, 88 (2) :189-196.
[18] Morschett H, Wiechert W, Oldiges M.Automation of a Nile red staining assay enables high throughput quantification of microalgal lipid production[J].Microbial Cell Factories, 2016, 15:34.
[19] Orr V, Rehmann L.Improvement of the Nile Red fluorescence assay for determination of total lipid content in microalgae independent of chlorophyll content[J].Journal of Applied Physics, 2015, 27 (6) :1-9.
[20] Rostron KA, Rolph CE, Lawrence CL.Nile red fluorescence screening facilitating neutral lipid phenotype determination in budding yeast, Saccharomyces cerevisiae, and the fission yeast Schizosaccharomyces pombe[J].Antonie Van Leeuwenhoek, 2015, 108 (1) :97-106.
[21] Wong DM, Nguyen TTN, Franz AK.Ethylenediaminetetraacetic acid (EDTA) enhances intracellular lipid staining with Nile red in microalgae Tetraselmis suecica[J].Algal Research, 2014, 5 (1) :158-163.
计量
- 文章访问数: 156
- HTML全文浏览量: 26
- PDF下载量: 277