EventsMOL2NET'17, Conference on Molecular, Biomed., Comput. & Network Science and Engineering, 3rd ed.
Published
This submission belongs to the session 06. NICEXSM-03: North-Ibero-American Congress on Exp. & Simul. Methods, Valencia, Bilbao, Spain-Paraiba, Brasil-Miami, USA, 2017 of the event MOL2NET'17, Conference on Molecular, Biomed., Comput. & Network Science and Engineering, 3rd ed.
Published date
27 Oct, 2017
Citation
Ángel Serrano-Aroca, Jerónimo Chirivella-Martorell, Direct spectrophotometric method to determine cell density of Isochrysis galbana in serial batch cultures from a larger scale fed-batch culture in exponential phase , in Proceedings of MOL2NET'17, Conference on Molecular, Biomed., Comput. & Network Science and Engineering, 3rd ed., 15 January–15 December 2017, MDPI: Basel, Switzerland, doi: 10.3390/mol2net-03-04632
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Direct spectrophotometric method to determine cell density of Isochrysis galbana in serial batch cultures from a larger scale fed-batch culture in exponential phase

Jerónimo Chirivella-Martorell 1
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1. Aquatic Resources Group. Institute of Environment and Marine Science Research (IMEDMAR). Universidad Católica de Valencia San Vicente Mártir, C/Guillem de Castro 94, 46001 Valencia, Spain
2. Biomaterials and Bioengineering Lab, Centro de Investigación Traslacional San Alberto Magno, Universidad Católica de Valencia San Vicente Mártir, c/Guillem de Castro 94, 46001 Valencia, Spain
Abstract

In this work, a very useful and accurate procedure, based on the spectrophotometric method published by the American Public Health Association in the Standards Methods for the Examination of Water and Wastewater, was developed to determine cell density of Isochrysis galbana performing a single direct absorbance measurement in exponential phase of growth, which is the desirable operating mode for any microalgae production plant. Thus, Isochrysis galbana was cultured in serial batch cultures from a larger scale fed-batch culture. The growth performance of this species of microalgae under laboratory conditions was analysed by spectrophotometry at different wavelengths and cell counting in a haemocytometer (Neubauer chamber) showing that doubling times and cell death increased with increasing initial cell density. Besides, it was demonstrated that the absorbance of these cultures followed a linear trend as a function of time and cell density during the exponential phase of growth, results in which the developed direct method is based on.

https://www.ucv.es/investigacion/publicaciones/catalogo-de-revistas/revista-nereis (NEREIS Nº9)

Keywords
Isochrysis galbana
batch
fed-batch culture
spectrophotometry
haemocytometer
growth performance
Poster
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