Development and characterization of a new Bombyx mori cell line for protein expression |
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Authors: | Arun M. Khurad Ravindra S. Bahekar Min-Juan Zhang Ashish D. Tiple Jae Man Lee Chuan-Xi Zhang Takahiro Kusakabe |
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Affiliation: | 1. Department of Zoology, RTM Nagpur University Campus, Nagpur 440 033, India;2. Molecular Biology Laboratory, Institute of Insect Sciences, Zijingang Campus, Zhejiang University, Yuhangtang Road 388, Hangzhou, 310058, China;3. Laboratory of Silkworm Science, Kyushu University Graduate School of Bioresource and Bioenvironmental Sciences, 6-10-1 Hakozaki, Higashi-ku Fukuoka 812–8581, Japan |
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Abstract: | A Bombyx mori continuous cell line, designated DZNU-Bm-17, was established from larval ovaries. The cells were initially grown in MGM-448 insect cell culture medium supplemented with 10% fetal bovine serum and 3% heat inactivated B. mori hemolymph at 25 ± 1 °C and later adapted gradually to TNM-FH medium. Partially adhered refractive cells were the predominant cell type in the culture. The cells took about 1055 days to complete 100 passages in TNM-FH medium. The population doubling time of the cell line was about 30–34 h at 25 ± 1 °C. The cell population was largely diploid, but a few triploids and tetraploids were also observed. DNA profiles using simple sequence repeat loci established the differences between the DZNU-Bm-1, Bm-5, DZNU-Bm-12, DZNU-Bm-17, and BmN cell lines. The cell line was susceptible to budded virus of B. mori nucleopolyhedrovirus (BmNPV), and 85–92% of the cells harbored BmNPV with an average of 15 occlusion bodies/infected cell. The cells expressed the luciferase and green fluorescent proteins using the BmNPV bacmid vector. We suggest the usefulness of the DZNU-Bm-17 cell line for BmNPV-based baculoviral expression studies. |
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