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      A silkworm based silk gland bioreactor for high-efficiency production of recombinant human lactoferrin with antibacterial and anti-inflammatory activities

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          Abstract

          Background

          Silk glands are used by silkworms to spin silk fibers for making their cocoons. These have recently been regarded as bioreactor hosts for the cost-effective production of other valuable exogenous proteins and have drawn wide attention.

          Results

          In this study, we established a transgenic silkworm strain which synthesizes the recombinant human lactoferrin (rhLF) in the silk gland and spins them into the cocoon by our previously constructed silk gland based bioreactor system. The yield of the rhLF with the highest expression level was estimated to be 12.07 mg/g cocoon shell weight produced by the transgenic silkworm strain 34. Utilizing a simple purification protocol, 9.24 mg of the rhLF with recovery of 76.55% and purity of 95.45% on average could be purified from 1 g of the cocoons. The purified rhLF was detected with a secondary structure similar with the commercially purchased human lactoferrin. Eight types of N-glycans which dominated by the GlcNAc (4) Man (3) (61.15%) and the GlcNAc (3) Man (3) (17.98%) were identified at the three typical N-glycosylation sites of the rhLF. Biological activities assays showed the significant evidence that the purified rhLF could relief the lipopolysaccharide (LPS)-induced cell inflammation in RAW264.7 cells and exhibit potent antibacterial bioactivities against the Escherichia coli ( E. coli) and Bacillus subtilis.

          Conclusions

          These results show that the middle silk gland of silkworm can be an efficient bioreactor for the mass production of rhLF and the potential application in anti-inflammation and antibacterial.

          Electronic supplementary material

          The online version of this article (10.1186/s13036-019-0186-z) contains supplementary material, which is available to authorized users.

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          Most cited references39

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          Mammalian glycosylation in immunity.

          Glycosylation produces a diverse and abundant repertoire of glycans, which are collectively known as the glycome. Glycans are one of the four fundamental macromolecular components of all cells, and are highly regulated in the immune system. Their diversity reflects their multiple biological functions that encompass ligands for proteinaceous receptors known as lectins. Since the discovery that selectins and their glycan ligands are important for the regulation of leukocyte trafficking, it has been shown that additional features of the vertebrate immune system are also controlled by endogenous cellular glycosylation. This Review focuses on the emerging immunological roles of the mammalian glycome.
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            Lactoferrin: structure, function and applications.

            Lactoferrin (LF) is an 80 kDa iron-binding glycoprotein of the transferrin family that is expressed in most biological fluids and is a major component of the mammalian innate immune system. Its protective effects range from direct antimicrobial activities against a large panel of microorganisms, including bacteria, viruses, fungi and parasites, to anti-inflammatory and anticancer activities. These extensive activities are made possible by mechanisms of action utilising not only the capacity of LF to bind iron but also interactions of LF with molecular and cellular components of both host and pathogens. This review summarises the putative antimicrobial mechanisms, clinical applications and heterologous expression models for LF.
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              Germline transformation of the silkworm Bombyx mori L. using a piggyBac transposon-derived vector.

              We have developed a system for stable germline transformation in the silkworm Bombyx mori L. using piggyBac, a transposon discovered in the lepidopteran Trichoplusia ni. The transformation constructs consist of the piggyBac inverted terminal repeats flanking a fusion of the B. mori cytoplasmic actin gene BmA3 promoter and the green fluorescent protein (GFP). A nonautonomous helper plasmid encodes the piggyBac transposase. The reporter gene construct was coinjected into preblastoderm eggs of two strains of B. mori. Approximately 2% of the individuals in the G1 broods expressed GFP. DNA analyses of GFP-positive G1 silkworms revealed that multiple independent insertions occurred frequently. The transgene was stably transferred to the next generation through normal Mendelian inheritance. The presence of the inverted terminal repeats of piggyBac and the characteristic TTAA sequence at the borders of all the analyzed inserts confirmed that transformation resulted from precise transposition events. This efficient method of stable gene transfer in a lepidopteran insect opens the way for promising basic research and biotechnological applications.
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                Author and article information

                Contributors
                +86-23-6825-0099 , xiaqy@swu.edu.cn
                Journal
                J Biol Eng
                J Biol Eng
                Journal of Biological Engineering
                BioMed Central (London )
                1754-1611
                5 July 2019
                5 July 2019
                2019
                : 13
                : 61
                Affiliations
                [1 ]GRID grid.263906.8, Biological Science Research Center, , Southwest University, ; Chongqing, 400716 China
                [2 ]GRID grid.263906.8, Chongqing Key Laboratory of Sericultural Science, , Southwest University, ; Chongqing, 400716 China
                [3 ]GRID grid.263906.8, Chongqing Engineering and Technology Research Center for Novel Silk Materials, , Southwest University, ; Chongqing, 400716 China
                Article
                186
                10.1186/s13036-019-0186-z
                6612213
                547f24a1-c781-40b7-961e-f3f7466b36ed
                © The Author(s). 2019

                Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License ( http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver ( http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

                History
                : 21 March 2019
                : 11 June 2019
                Funding
                Funded by: the National Natural Science Foundation of China
                Award ID: 31530071
                Award Recipient :
                Funded by: the Chongqing Science & Technology Commission
                Award ID: cstc2018jcyjAX0298
                Award Recipient :
                Funded by: State key laboratory of silkworm genome biology
                Award ID: sklsgb1819-1
                Award Recipient :
                Funded by: Fundamental Research Funds for the Central Universities
                Award ID: XDJK2018C064
                Award Recipient :
                Funded by: Chongqing Engineering and Technology Research Center for Novel Silk Materials
                Award ID: grant number SILKGCZX2016002
                Award Recipient :
                Funded by: Municipal Graduate Student Research Innovation Project of Chongqing
                Award ID: grant number CYB17066
                Award Recipient :
                Categories
                Research
                Custom metadata
                © The Author(s) 2019

                Biotechnology
                recombinant human lactoferrin,high-efficiency production,silkworm,glycosylation modification

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