Gene cloning and expression characteristics of vacuolar-type ATPase subunit B in Bombyx mori.
- Author:
Huifang CHEN
1
;
Xin WANG
1
;
Kang XIE
1
;
Yi LI
1
;
Ping ZHAO
1
Author Information
- Publication Type:Journal Article
- Keywords: BmV-ATPase B; Western blotting; gene cloning; immunofluorescence localization; prokaryotic expression; silkworm (Bombyx mori)
- MeSH: Animals; Bombyx; enzymology; Cloning, Molecular; Escherichia coli; metabolism; Insect Proteins; genetics; metabolism; Larva; Recombinant Proteins; genetics; metabolism; Silk; Vacuolar Proton-Translocating ATPases; genetics; metabolism
- From: Chinese Journal of Biotechnology 2016;32(4):487-496
- CountryChina
- Language:Chinese
- Abstract: Vacuolar-type ATPase (V-ATPase), located in the membrane and organelle membrane, is one of important H⁺-transporting proteins. It keeps the proton balance by transporting H⁺ into vacuole, vesicle, or extracellular using the energy from ATP hydrolysis. The subunit B of the vacuolar-type ATPase (BmV-ATPase B) contains the ATP catalytic site, and plays an important role in this process. To study the function of V-ATPase B in Bombyx mori (BmV-ATPase B), we cloned its coding gene from the midgut of the 5th instar silkworm larvae. Then we constructed prokaryotic expression vector and produced the recombinant protein in E. coli. The recombinant protein was identified as BmV-ATPase B by mass spectrometry and purified using Ni-NTA affinity chromatography. This purified protein was used to immunize rabbit to generate polyclonal antibodies of BmV-ATPase B. Finally, the expression patterns of BmV-ATPase B in the silk gland were analyzed by western blotting and immunofluorescence. The full length CDS sequence of BmV-ATPase B was 1 473 bp. BmV-ATPase B was 55 kDa with a PI of 5.3. We analyzed the expression patterns of BmV-ATPase B in different sections of silk gland from the silkworm on the 3rd day of 5th instar and 1st day of wander stage by western blotting. BmV-ATPase B was expressed in all sections of the silk gland and it was abundant in the anterior silk gland (ASG) both in these two developmental stages. Furthermore, immunofluorescence indicated that BmV-ATPase B was located in the silk gland cells. Laser confocal scanning microscopy analysis revealed that BmV-ATPase B was mainly expressed in the cytomembrane of silk gland cells. These data elucidated the expression patterns of BmV-ATPase B in the silk gland of silkworm, which provides a good basis for further studies on the function of V-ATPase B in silk fiber formation.
