Measurement of light and pH dependence of single-cell photosynthesis by fluorescence microscopy
Measurement of algal photosynthetic performance with conventional methods requires thousands of cells obtained by isolation and subsequent cultivation. This is a time-consuming process for many species. We describe a new method to study photosynthetic performance of single algal cells under various...
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Published in | Journal of fluorescence Vol. 10; no. 3; pp. 269 - 273 |
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Main Authors | , |
Format | Journal Article |
Language | English |
Published |
01.09.2000
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Abstract | Measurement of algal photosynthetic performance with conventional methods requires thousands of cells obtained by isolation and subsequent cultivation. This is a time-consuming process for many species. We describe a new method to study photosynthetic performance of single algal cells under various environmental conditions by a combination of modulated chlorophyll fluorescence, light microscopy, and sample manipulation techniques. Single cell fluorescence was measured with a modulated microfluorometer integrated in an inverted microscope. The algal cell was sucked onto the tip of a glass microcapillary and positioned in the center of the field of view of the microscope by a micromanipulator. A superfusion device was used to generate a flow of experimental solution of variable composition along the alga. The light dependence of Scenedesmus obtusiusculus single-cell photosystem II (PSII) electron flow was measured at various pH. At a high intensity PSII electron flow was inhibited at pH 6.5 and higher, while at a low light inhibition occurred at pH 9.5. This is in agreement with inhibition of photosynthesis by substrate (CO sub(2)) limitation at alkaline pH. This approach can easily be extended to study the in vivo effects of other abiotic parameters (temperature, nutrients, toxicants, oxygen) on the photosynthetic performance of algae. |
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AbstractList | Measurement of algal photosynthetic performance with conventional methods requires thousands of cells obtained by isolation and subsequent cultivation. This is a time-consuming process for many species. We describe a new method to study photosynthetic performance of single algal cells under various environmental conditions by a combination of modulated chlorophyll fluorescence, light microscopy, and sample manipulation techniques. Single cell fluorescence was measured with a modulated microfluorometer integrated in an inverted microscope. The algal cell was sucked onto the tip of a glass microcapillary and positioned in the center of the field of view of the microscope by a micromanipulator. A superfusion device was used to generate a flow of experimental solution of variable composition along the alga. The light dependence of Scenedesmus obtusiusculus single-cell photosystem II (PSII) electron flow was measured at various pH. At a high intensity PSII electron flow was inhibited at pH 6.5 and higher, while at a low light inhibition occurred at pH 9.5. This is in agreement with inhibition of photosynthesis by substrate (CO sub(2)) limitation at alkaline pH. This approach can easily be extended to study the in vivo effects of other abiotic parameters (temperature, nutrients, toxicants, oxygen) on the photosynthetic performance of algae. |
Author | Snel, Jan FH Dassen, Hans HA |
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CitedBy_id | crossref_primary_10_1016_S1369_5266_00_00161_8 crossref_primary_10_1128_MMBR_68_3_538_559_2004 crossref_primary_10_1007_s11120_016_0318_y crossref_primary_10_1002_etc_2290 crossref_primary_10_1016_j_bbabio_2007_01_004 crossref_primary_10_1007_s11356_019_07068_9 crossref_primary_10_1007_s00227_011_1663_1 crossref_primary_10_1088_2050_6120_ab77f4 crossref_primary_10_1007_s11120_012_9754_5 crossref_primary_10_1080_09670260600937791 crossref_primary_10_1007_s11120_009_9500_9 crossref_primary_10_1080_14634980490513364 |
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SubjectTerms | Carbon dioxide Cells Electrons Fluorescence Fluorometers Microscopes Optical microscopy pH effects Photosynthesis Substrates |
Title | Measurement of light and pH dependence of single-cell photosynthesis by fluorescence microscopy |
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