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Monitoring and rapid quantification of  total carotenoids in Rhodotorula glutinis  cells using laser tweezers Raman spectroscopy
Author(s) -
Tao Zhanhua,
Wang Guiwen,
Xu Xiaodong,
Yuan Yufeng,
Wang Xue,
Li Yongqing
Publication year - 2011
Publication title -
fems microbiology letters
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.899
H-Index - 151
eISSN - 1574-6968
pISSN - 0378-1097
DOI - 10.1111/j.1574-6968.2010.02139.x
Subject(s) - carotenoid , rhodotorula , optical tweezers , nucleic acid , raman spectroscopy , biology , biochemistry , biophysics , chemistry , yeast , optics , physics
Rhodotorula glutinis is known to accumulate large amounts of carotenoids under certain culture conditions, which have very important industrial applications. So far, the molecular mechanism of regulating carotenogenesis is still not well understood. To better understand the carotenogenesis process, it requires methods that can detect carotenogenesis rapidly and reliably in single live cells. In this paper, a method based on laser tweezers Raman spectroscopy (LTRS) was developed to directly detect carotenoids, as well as other important biological molecules in single live R. glutinis cells. The data showed that the accumulation of carotenoids and lipids occurred mainly in the late exponential and stationary phases when the cell growth was inhibited by nutrient limitation. Meanwhile, the carotenoid concentration changed together with the concentration of nucleic acids, which increased in the first phase and decreased in the last phase of the culture. These data demonstrate that LTRS is a rapid, convenient, and reliable method to study the carotenogenesis process in vivo .

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