Araştırma Makalesi

Recombinant Production of Hydrophobin DewA in Pichia pastoris and Determination of Its Functions

Cilt: 7 Sayı: 1 15 Nisan 2024
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Recombinant Production of Hydrophobin DewA in Pichia pastoris and Determination of Its Functions

Öz

Background Hydrophobins have great potential in many biotechnological applications due to changing surface characteristics. In recent years, although there has been a significant increase in the biotechnological applications of hydrophobins, industrial production has still not been achieved due to yield problems. Therefore, more studies are needed on the recombinant production of hydrophobins. In this work, the recombinant production of class I hydrophobin DewA from Aspergillus nidulans, which is determined to have high contact angle in the literature, was aimed. As a result, DewA protein was recombinantly produced using P. pastoris X-33 strain under AOX1 promoter by transferring into pPICZα-A vector. Results The optimal culture condition for DewA expression was obtained at 1% methanol concentration as 77 mg/L in 96 hour. Recombinant DewA has been proven to change the surface characteristics on the teflon and glass surfaces. Then, the surface stability of the protein was evaluated by applying hot SDS and UV to these surfaces. The surface-coated DewA was resistant to hot SDS application on both glass and teflon surfaces; in the UV application, it was understood that while the protein was degraded by UV exposure on glass surfaces, it preserved its structure on teflon surfaces. Conclusions In the study, the DewA protein of A.nidulans was cloned into the pPICZα-A vector and recombinantly produced in the P.pastoris X-33 strain for the first time.

Anahtar Kelimeler

Destekleyen Kurum

Erzurum Teknik Üniversitesi

Proje Numarası

This study was supported by Erzurum Technical University BAP coordination unıt with the project numbered 2019/11.

Teşekkür

The authors would like to thank Erzurum Technical University for their financial support for the project.

Kaynakça

  1. Sarlin, T., et al. İdentification and characterization of gushing-active hydrophobins from Fusarium graminearum and related species. J Basic Microbiol, 2012. (52)2: p.184-194. doi: https://doi.org/10.1002/jobm.201100053
  2. Ren, Q., Kwan, A.K., Sunde, M. Two forms and two faces, multiple states and multiple uses: Properties and applications of the self-assembling fungal hydrophobins Biopolymers, 2013. (100)6: p. 601– 612. doi: https://doi.org/10.1002/bip.22259
  3. Bayry, J., et al. Hydrophobins Unique fungal proteins. PLoS pathog, 2012. (8)5: p.1-16. doi: 10.1371/journal.ppat.1002700.
  4. Wösten, H.A. and Scholtmeijer, K. Applications of hydrophobins: current state and perspectives. Appl Microbiol Biotechnol, 2015. 99: p.1587–1597. doi: https://doi.org/10.1007/s00253-014-6319-x
  5. Kulkarni, S., Nene, S., Joshi, K. Production of Hydrophobins from fungi. Biocatal Agric Biotechnol, 2017. 61: p.1-11. https://doi.org/10.1016/j.procbio.2017.06.012
  6. Rabe, M., Verdes, D., Seeger, S. Understanding protein adsorption phenomena at solid surfaces. Adv Colloid Interface Sci, 2011. (162) 2: p.87-106. https://doi.org/10.1016/j.cis.2010.12.007
  7. Linder, M.B., et al. Hydrophobins: the protein-amphiphiles of filamentous fungi, FEMS Microbiol Rev, 2005. (29)5: p.877 896. https://doi.org/10.1016/j.femsre.2005.01.004
  8. Demain, A.L., Vaishnav, P. Production of recombinant proteins by microbes and higher organisms. Biotechnology Advances. 2009. (27)3: p. 297–306. doi: https://doi.org/10.1016/j.femsre.2005.01.004

Ayrıntılar

Birincil Dil

İngilizce

Konular

Gen Haritalaması, Genom Yapısı ve Düzenlemesi, Genetik (Diğer), Mikrobiyoloji (Diğer)

Bölüm

Araştırma Makalesi

Erken Görünüm Tarihi

21 Nisan 2024

Yayımlanma Tarihi

15 Nisan 2024

Gönderilme Tarihi

7 Eylül 2023

Kabul Tarihi

10 Ekim 2023

Yayımlandığı Sayı

Yıl 2024 Cilt: 7 Sayı: 1

Kaynak Göster

APA
Turgut, A., Yazıcı, A., Taşkın, M., & Örtücü, S. (2024). Recombinant Production of Hydrophobin DewA in Pichia pastoris and Determination of Its Functions. International Journal of Life Sciences and Biotechnology, 7(1), 12-20. https://doi.org/10.38001/ijlsb.1355883
AMA
1.Turgut A, Yazıcı A, Taşkın M, Örtücü S. Recombinant Production of Hydrophobin DewA in Pichia pastoris and Determination of Its Functions. Int J. Life Sci. Biotechnol. 2024;7(1):12-20. doi:10.38001/ijlsb.1355883
Chicago
Turgut, Alpgiray, Ayşenur Yazıcı, Mesut Taşkın, ve Serkan Örtücü. 2024. “Recombinant Production of Hydrophobin DewA in Pichia pastoris and Determination of Its Functions”. International Journal of Life Sciences and Biotechnology 7 (1): 12-20. https://doi.org/10.38001/ijlsb.1355883.
EndNote
Turgut A, Yazıcı A, Taşkın M, Örtücü S (01 Nisan 2024) Recombinant Production of Hydrophobin DewA in Pichia pastoris and Determination of Its Functions. International Journal of Life Sciences and Biotechnology 7 1 12–20.
IEEE
[1]A. Turgut, A. Yazıcı, M. Taşkın, ve S. Örtücü, “Recombinant Production of Hydrophobin DewA in Pichia pastoris and Determination of Its Functions”, Int J. Life Sci. Biotechnol., c. 7, sy 1, ss. 12–20, Nis. 2024, doi: 10.38001/ijlsb.1355883.
ISNAD
Turgut, Alpgiray - Yazıcı, Ayşenur - Taşkın, Mesut - Örtücü, Serkan. “Recombinant Production of Hydrophobin DewA in Pichia pastoris and Determination of Its Functions”. International Journal of Life Sciences and Biotechnology 7/1 (01 Nisan 2024): 12-20. https://doi.org/10.38001/ijlsb.1355883.
JAMA
1.Turgut A, Yazıcı A, Taşkın M, Örtücü S. Recombinant Production of Hydrophobin DewA in Pichia pastoris and Determination of Its Functions. Int J. Life Sci. Biotechnol. 2024;7:12–20.
MLA
Turgut, Alpgiray, vd. “Recombinant Production of Hydrophobin DewA in Pichia pastoris and Determination of Its Functions”. International Journal of Life Sciences and Biotechnology, c. 7, sy 1, Nisan 2024, ss. 12-20, doi:10.38001/ijlsb.1355883.
Vancouver
1.Alpgiray Turgut, Ayşenur Yazıcı, Mesut Taşkın, Serkan Örtücü. Recombinant Production of Hydrophobin DewA in Pichia pastoris and Determination of Its Functions. Int J. Life Sci. Biotechnol. 01 Nisan 2024;7(1):12-20. doi:10.38001/ijlsb.1355883


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