Study of the Growth Curve of Vero Cell with Statistical Counting Method Based on the SEM Images

2001 ◽  
Vol 7 (S2) ◽  
pp. 46-47
Author(s):  
Manjun Shao ◽  
Lei Jiang

For industrial-scale culture of anchorage-dependent mammalian cell, such as vero cell, growth on the microcarriers offers certain advantages. As previous research reported, growth process can be illustrated by a growth curve - cell density versus time, which shows the change of cell density through whole growth process including: first adhesion stage; spreading and division stage; and last confluent stage. The growth curves are controlled by the culture condition (culture medium, temperature, pH value, inoculation concentration, etc.) and space condition (kind of microcarrier, microcarrier size, and surface property, etc.). Therefore, the cell growth curve is not only the important basis for studying growth kinetics, but also for designing biological reactors.Traditionally, total cell concentration for the microcarrier cultures were determined using the crystal violet method, and the cell nuclei were counted with a hemacytometer. in this method, the cells attached on each microcarrier were trypsinized and dyed by crystal violet dye, so that the number of nuclei counted was statistically representative. in this work, the cells and microcarriers were examined by using an environmental SEM - KYKY1500. As a result, the moist cells and microcarriers in SEM images show their natural characteristics, because this environmental SEM permits biological sample to be observed directly in an environmental specimen chamber without normal preparation for biological sample. As for the normal preparation, it needs a long duration, e.g. 2 days normally, to do fixing, desiccating and gold-coating. in contrast, the operation for observation of the biological samples in this SEM is much simpler. in view of this, a statistical counting method based on the SEM images for determining cell concentration during microcarrier culture was developed.

2016 ◽  
Vol 78 (7) ◽  
Author(s):  
Costantine Joannes ◽  
Rachel Fran Mansa ◽  
Suhaimi Md. Yasir ◽  
Jedol Dayou

Lately, research on biodiesel production as a renewable and sustainable energy has become increasingly apparent due to the fact that fossil fuel is decreasing and the concern of global warming issues. The third generation of biofuel, which is microalgae-based biodiesel had gained interest over the last decade. The ability of microalgae to grow in various conditions is one of its advantages as the potential and promising feedstock for biodiesel. Microalgae can be cultivated in three modes such as photoautotrophic, heterotrophic and mixotrophic culture mode. Unlike photoautotrophic mode where light is required, the heterotrophic mode mainly utilized carbon compounds to grow. On the other hand, the mixotrophic mode is the condition where light and carbon compounds are supplied for microalgae culturing. This paper investigates the cell growth of Chlorella sp. cultivated in photoautotrophic, heterotrophic and mixotrophic culture mode. It was found that Chlorella sp. was capable of producing the highest cell concentration of 6.67 ± 0.56 x 106 cell mL-1 in the photoautotrophic mode for 23 days of cultivation period. This was 1.3 times and 3.2 times greater than the cell concentration in mixotrophic (5.02 ± 0.49 x 106 cell mL-1) and heterotrophic (2.03 ± 0.29 x 106 cell mL-1) culture, respectively. On the contrary, the highest specific growth rate obtained in the study was from heterotrophic mode (0.32 ± 0.04 day-1) followed by photoautotrophic and mixotrophic mode with 0.26 ± 0.05 day-1 and 0.20 ± 0.04 day-1, respectively. Chlorella sp. cell grew well under the photoautotrophic and mixotrophic mode. However, the insufficient of glucose level had contributed to lower cells productivity in the heterotrophic culture. Therefore, the mixotrophic mode could also be an alternative pathway in microalgae cultivation for biodiesel production if the glucose supplied was adequate and at the suitable level.  


2014 ◽  
Vol 38 (3) ◽  
pp. 543-555 ◽  
Author(s):  
Ramona V. Ursache ◽  
Yvonne E. Thomassen ◽  
Gerco van Eikenhorst ◽  
Peter J. T. Verheijen ◽  
Wilfried A. M. Bakker

2006 ◽  
Vol 41 (12) ◽  
pp. 2386-2392 ◽  
Author(s):  
Haiyan Huang ◽  
Xiaoping Yi ◽  
Yuanxing Zhang
Keyword(s):  

1986 ◽  
Vol 81 (1) ◽  
pp. 65-103
Author(s):  
A.T. Nahapetian ◽  
J.N. Thomas ◽  
W.G. Thilly

This study was initiated for optimization of the environment of a technologically useful mammalian cell line for high density production. Cultures of Vero cells on microcarriers were perfused with 100%, 50%, 25% and 12.5% modified L15 media (galactose was replaced with 10 mM-fructose, with 4 mM-glutamine and 5% foetal bovine serum) in phosphate-buffered saline at either 4 or 8 vol. day-1. Cell growth, pH, dissolved oxygen, and changes in the metabolites, lactate to pyruvate and lactate to ammonia indices, demonstrated that under the conditions used in the present study, perfusion of cultures with 50% L15 medium in PBS at 8 vol. day-1 provided the optimum microenvironment for Vero cell growth. The highest cell density in the perfused cultures was 3 X 10(7) cells ml-1, which at these conditions was ten times higher than the maximum cell density (3 X 10(6) cells ml-1) obtained in a batch culture. Nutrient supply and conditioning factors were the most probable growth-limiting factors in cultures that were perfused with 12.5% and 25% L15 media, while multilayering, limitation of available oxygen, and accumulation of metabolic end products in the cellular microenvironment were the most probable causes of a density-dependent inhibition of cell growth observed under the optimized and overfed (supply of 100% L15 medium at the rate of 8 vol. day-1) culture conditions. Under the optimized environmental condition, the major source of energy was probably glutamine during the first week. However, significant utilization of fructose became evident at higher cell densities during the second week, when lactate production dramatically declined and reached an almost undetectable level, while respiration progressively assumed the predominant role in energy production. It is postulated that ‘available’ oxygen in the multicell-layered microenvironment of the optimized cultures was higher than in the overfed culture due to the greater utilization rate of oxygen for oxidation of excess nutrients in the overfed culture.


2021 ◽  
Author(s):  
Luman Wang ◽  
Jianxin Wang ◽  
Huiying Qi

Abstract To detect the mechanism of growth, volume is important to uncover the genetic basis of dynamic complex quantitative traits. Unfortunately, it is difficult to construct the unique simple growth curve to accurately describe the growth process of all trees by the conventional GWAS based on the functional mapping method, which reduces the power of statistics for the growth model. To address this issue, this work adopted a novel approach about the Earliness degree index (E-index). First, it adopted the method of spline interpolation to fit the growth data to acquire the growth curves for each tree. Second, an innovative calculation model based on E-index was used to measure the earliness degree for each growth curve and to identify the potential relationship between QTL effects and traits by a series of hypothesis tests. Besides, a permutation test could be used to estimate the threshold for p values and to screen out significant QTLs from SNPs related to the growth process. To verify the validity and practicability of our model, we applied this method on the data about the volumes of 64 poplar trees chosen randomly from the progeny of two poplar species I-69 and I-45 with 156362 single nucleotide polymorphisms (SNPs). Through the E-index method, 13 significant markers were identified for testcross and 10 for intercross related to the growth process. Overall, this study could help elucidate the underlying genetic mechanisms of complex dynamic traits and perform marker-assisted selection in poplar.


2001 ◽  
Vol 7 (S2) ◽  
pp. 834-835 ◽  
Author(s):  
Andrew J. Marshall ◽  
Buddy D. Ratner

Introduction Applications for porous biomaterials include scaffolds for tissue engineering and spatial control of wound healing. Porous hydrogels are of particular interest due to their hydrophilic nature, elasticity, and mechanical compatibility with soft tissues. We present an optical technique for quantitatively analyzing the pore structure of porous hydrogel materials. The technique presented here is especially useful for analyzing a new class of porous hydrogels with spherical pore shape. Many important properties of the three-dimensional pore structure of these materials can be quantitatively described by analyzing a twodimensional slice (thin section) of material.Materials and MethodsPorous cross-linked hydrogels were prepared using a previously described method. Briefly, poly(hydroxyethyl methacrylate) (polyHEMA) was polymerized around a pore template of close-packed poly(methyl methacrylate) (PMMA) microspheres (Sekisui Plastics, grade MB-8C or MB-20C). The microspheres were then leached out with 90% v/v acetone.Scanning electron microscope (SEM) images were obtained using an FEI 2020 Environmental SEM with a gun voltage of 15 kV and a chamber pressure of 5 torr.


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