Microfluidic cytometer for high-throughput measurement of photosynthetic characteristics and lipid accumulation in individual algal cells

被引:29
作者
Erickson, Richard A. [1 ,2 ]
Jimenez, Ralph [1 ,2 ,3 ]
机构
[1] Univ Colorado, Joint Inst Lab Astrophys, Boulder, CO 80309 USA
[2] Natl Inst Stand & Technol, Boulder, CO 80309 USA
[3] Univ Colorado, Dept Chem & Biochem, Boulder, CO 80309 USA
基金
美国国家科学基金会;
关键词
CHLOROPHYLL FLUORESCENCE; MARINE-PHYTOPLANKTON; PHOTOSYSTEM-II; FLOW CYTOMETER; QUANTUM YIELD; RAPID METHOD; NILE RED; MICROALGAE; INDUCTION; EXTRACTION;
D O I
10.1039/c3lc41429a
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Commercially viable algal biofuel production requires discovery of new strains, genetic engineering for higher productivity and optimization of growth conditions. To accelerate research in these areas, we developed a microfluidic cytometer that measures forward light scatter, chlorophyll fluorescence induction and lipophilic stain fluorescence at a rate of 100 cells s(-1). The chlorophyll fluorescence data is processed in real-time to measure the fluorescence-based maximum quantum yield, reported as F-v/F-m, to quantify the photochemical energy conversion of each cell. To demonstrate instrument performance, F-v/F-m measurements are obtained for unstressed (nutrient-replete) and stressed (nutrient-limited) cultures of the marine diatom Phaeodactylum tricornutum and are correlated to values obtained in bulk samples using traditional pulse-amplitude-modulating fluorometry. We then use the cytometer to characterize unstressed and stressed P. tricornutum and show that lipid content (as measured by Nile Red fluorescence) is inversely correlated with F-v/F-m. We believe these findings to be the first time that both photosynthetic efficiency and lipid accumulation have been simultaneously evaluated at the single cell level, and that in doing so, the diversity within these populations was revealed.
引用
收藏
页码:2893 / 2901
页数:9
相关论文
共 44 条
[1]  
AHLGREN G, 1991, ARCH HYDROBIOL, V121, P295
[2]  
[Anonymous], 1962, STAT PRINCIPLES EXPT
[3]   Physiological stress and cell death in marine phytoplankton: Induction of proteases in response to nitrogen or light limitation [J].
Berges, JA ;
Falkowski, PG .
LIMNOLOGY AND OCEANOGRAPHY, 1998, 43 (01) :129-135
[4]   PHOTON YIELD OF O-2 EVOLUTION AND CHLOROPHYLL FLUORESCENCE CHARACTERISTICS AT 77-K AMONG VASCULAR PLANTS OF DIVERSE ORIGINS [J].
BJORKMAN, O ;
DEMMIG, B .
PLANTA, 1987, 170 (04) :489-504
[5]  
BLIGH EG, 1959, CAN J BIOCHEM PHYS, V37, P911
[6]   Optical microflow cytometer for particle counting, sizing and fluorescence detection [J].
Chen, Han-Taw ;
Wang, Yao-Nan .
MICROFLUIDICS AND NANOFLUIDICS, 2009, 6 (04) :529-537
[7]   Microwave-assisted Nile red method for in vivo quantification of neutral lipids in microalgae [J].
Chen, Wei ;
Sommerfeld, Milton ;
Hu, Qiang .
BIORESOURCE TECHNOLOGY, 2011, 102 (01) :135-141
[8]   A high throughput Nile red method for quantitative measurement of neutral lipids in microalgae [J].
Chen, Wei ;
Zhang, Chengwu ;
Song, Lirong ;
Sommerfeld, Milton ;
Hu, Qiang .
JOURNAL OF MICROBIOLOGICAL METHODS, 2009, 77 (01) :41-47
[9]   Review Article: Recent advancements in optofluidic flow cytometer [J].
Cho, Sung Hwan ;
Godin, Jessica M. ;
Chen, Chun-Hao ;
Qiao, Wen ;
Lee, Hosuk ;
Lo, Yu-Hwa .
BIOMICROFLUIDICS, 2010, 4 (04)
[10]   Optimization of staining conditions for microalgae with three lipophilic dyes to reduce precipitation and fluorescence variability [J].
Cirulis, Judith T. ;
Strasser, Bridget C. ;
Scott, John A. ;
Ross, Gregory M. .
CYTOMETRY PART A, 2012, 81A (07) :618-626