Abstract
In the present work, we tried to identify the mechanism why by which the steroid alcohols accumulated when hydroxypropyl-β-cyclodextrin (HP-β-CD) was present to enhance the sterol conversion rate. Compared with the bioconversion system without HP-β-CD, the reaction rate was greatly improved in presence of HP-β-CD, but the steroid alcohols largely accumulated concurrently. In a reaction system with an enhanced reaction rate, the higher intracellular NADH/NAD+ level was detected, and the production of steroid alcohols increased also. Mycobacterium neoaurum mutants with higher KshA activity (3-ketosteroid 9α-hydrolase, a monooxygenase hydroxylating the nucleus at C-9 at the expense of NAD(P)H consumption) reduced the steroid alcohol production, and in the meantime, the NADH/NAD+ level was decreased consequently. Further research found that oxygen availability was seriously inhibited by the cyclodextrin in a reaction system. These results indicated that NADH formed in the bioconversion was not properly regenerated via the respiratory chain because of the poor oxygen bioavailability. The inhibitory effect of cyclodextrin on oxygen bioavailability is a key factor for the metabolic flux redistribution toward steroid alcohols in phytosterol resting cells bioconversion.





Similar content being viewed by others
Explore related subjects
Discover the latest articles and news from researchers in related subjects, suggested using machine learning.References
Donova, M. V., & Egorova, O. V. (2012). Microbial steroid transformations: Current state and prospects. Applied Microbiology and Biotechnology, 94(6), 1423–1447.
Szentirrnai, A. (1990). Microbial physiology of sidechain degradation of sterols. Journal of Industrial Microbiology & Biotechnology, 6(2), 101–115.
Rodríguez-García, A., Fernández-Alegrea, E., Morales, A., Sola-Landa, A., Lorrainec, J., Macdonald, S., Dovbnya, D., Smith, M. C. M., Donova, M., & Barreiro, C. (2016). Complete genome sequence of ‘Mycobacterium neoaurum’ NRRL B-3805, an androstenedione (AD) producer for industrial biotransformation of sterols. Journal of Biotechnology, 224, 64–65.
van der Geize, R., Yam, K., Heuser, T., Wilbrink, M. H., Hara, H., Anderton, M. C., Sim, E., Dijkhuizen, L., Davies, J. E., Mohn, W. W., & Eltis, L. D. (2007). A gene cluster encoding cholesterol catabolism in a soil actinomycete provides insight into Mycobacterium tuberculosis survival in macrophages. Proceedings of the National Academy of Sciences, 104(6), 1947–1952.
Fernandez de las Herasa, L., van der Geizeb, R., Drzyzgaa, O., Pereraa, J., & Navarro Llorensa, J. M. (2012). Molecular characterization of three 3-ketosteroid-1-dehydrogenase isoenzymes of Rhodococcus ruber strain Chol-4. Journal of Steroid Biochemistry and Molecular Biology, 132, 271–281.
Liu, H. H., Xu, L. Q., Yao, K., Xiong, L. B., Tao, X. Y., Liu, M., Wang, F. Q., & Wei, D. Z. (2018). Engineered 3-ketosteroid 9α-hydroxylases in Mycobacterium neoaurum: An efficient platform for production of steroid drugs. Applied and Environmental Microbiology, 84(14), e02777–e02717.
Yeh, C. H., Kuo, Y. S., Chang, C. M., Liu, W. H., Sheu, M. L., & Meng, M. (2014). Deletion of the gene encoding the reductase component of 3-ketosteroid 9α-hydroxylase in Rhodococcus equi USA-18 disrupts sterol catabolism, leading to the accumulation of 3-oxo-23,24-bisnorchola-1,4-dien-22-oic acid and 1,4-androstadiene-3,17-dione. Microbial Cell Factories, 13, 130.
Yuan, J. J., Guan, Y. X., & Yao, S. J. (2017). Evaluation of biocompatible ionic liquids for their application in phytosterols bioconversion by Mycobacterium sp. resting cells. ACS Sustainable Chemistry & Engineering, 5(11), 10702–10709.
Stefanov, S., Yankov, D., & Beschkov, V. (2006). Biotransformation of phytosterols to androstenedione in two phase water-oil systems. Chemical and Biochemical Engineering Quarterly, 20(4), 421–427.
Shen, Y. B., Wang, M., Li, H. N., Wang, Y. B., & Luo, J. M. (2012). Influence of hydroxypropyl-β-cyclodextrin on phytosterol biotransformation by different strains of Mycobacterium neoaurum. Journal of Industrial Microbiology & Biotechnology, 39(9), 1253–1259.
Donova, M. V., Nikolayeva, V. M., Dovbnya, D. V., Gulevskaya, S. A., & Suzina, N. E. (2007). Methyl-β-cyclodextrin alters growth, activity and cell envelope features of sterol-transforming mycobacteria. Microbiology, 153(6), 1981–1992.
Khomutov, S. M., Sukhodolskaya, G. V., & Donova, M. V. (2017). The inhibitory effect of cyclodextrin on the degradation of 9α-hydroxyandrost-4-ene-3,17-dione by Mycobacterium sp. VKM Ac-1817D. Biocatalysis and Biotransformation, 25, 386–392.
Shtratnikova, V. Y., Schelkunov, M. I., Dovbnya, D. V., Bragin, E. Y., & Donova, M. V. (2017). Effect of methyl-β-cyclodextrin on gene expression in microbial conversion of phytosterol. Applied Microbiology and Biotechnology, 101(11), 4659–4667.
Gao, X. Q., Feng, J. X., Wang, X. D., Hua, Q., & Wei, D. Z. (2015). Enhanced steroid metabolites production by resting cell phytosterol bioconversion. Chemical and Biochemical Engineering Quarterly, 29(4), 567–573.
Zhou, X. L., Zhang, Y., She, Y. B., Zhang, X., Xu, S. P., Shang, Z. H., Xia, M. L., & Wang, M. (2019). Efficient production of androstenedione by repeated batch fermentation in waste cooking oil media through regulating NAD+/NADH ratio and strengthening cell vitality of Mycobacterium neoaurum. Bioresource Technology, 279, 209–217.
Wang, X. D., Chen, R., Wu, Y. Y., Wang, D., & Wei, D. Z. (2020). Nitrate metabolism decreases the steroidal alcohol byproduct compared with ammonium in biotransformation of phytosterol to androstenedione by Mycobacterium neoaurum. Applied Biochemistry and Biotechnology, 190(4), 1553–1560.
Yao, K., Xu, L. Q., Wang, F. Q., & Wei, D. Z. (2014). Characterization and engineering of 3-ketosteroid-Δ1-dehydrogenase and 3-ketosteroid-9α-hydroxylase in Mycobacterium neoaurum ATCC 25795 to produce 9α-hydroxy-4-androstene-3,17-dione through the catabolism of sterols. Metabolic Engineering, 24, 181–191.
Wang, X. D., Hua, C. L., Xu, X. W., & Wei, D. Z. (2019). Two-step bioprocess for reducing nucleus degradation in phytosterol bioconversion by Mycobacterium neoaurum NwIB-R10hsd4A. Applied Biochemistry and Biotechnology, 188(1), 138–146.
Petrusma, M., van der Geize, R., & Dijkhuzzzizen, L. (2014). 3-Ketosteroid 9a-hydroxylase enzymes: Rieske non-heme monooxygenases essential for bacterial steroid degradation. Antonie Van Leeuwenhoek, 106(1), 157–172.
Chen, X. L., Li, S. B., & Liu, L. M. (2014). Engineering redox balance through cofactor systems. Trends in Biotechnology, 32(6), 337–343.
Van Hoek, M. J., & Merks, R. M. H. (2012). Redox balance is key to explaining full vs. partial switching to low-yield metabolism. BMC Systems Biology, 6, 22.
Capyk, J. K., Kalscheuer, R., Stewart, G. R., Liu, J., Kwon, H., Zhao, R., Okamoto, S., Jacobs Jr., W. R., Eltis, L. D., & Mohn, W. W. (2009). Mycobacterial cytochrome P450 125 (Cyp125) catalyzes the terminal hydroxylation of C27-steroids. Journal of Biological Chemistry, 284(51), 35534–35542.
Badejo, A. C., Chung, W. H., Kim, N. S., Chai, J. C., Lee, Y. S., Jung, K. H., Kim, H. J., & Chai, Y. G. (2014). Energy metabolism in Mycobacterium gilvum PYR-GCK: Insights from transcript expression analyses following two states of induction. PLoS One, 9(6), 99464.
García, J. L., Uhía, I., & Galán, B. (2012). Catabolism and biotechnological applications of cholesterol degrading bacteria. Microbial Biotechnology, 5(6), 679–699.
Acknowledgements
This work was supported by the National Natural Science Foundation of China (31570079, 21276083).
Author information
Authors and Affiliations
Contributions
Xue-Dong Wang designed the experiments. Kuan Chen and Dan-Dan Cao performed the experiments. Xue-Dong Wang and Dong-Zhi Wei analyzed the experimental data and wrote the manuscript. All authors discussed the results and commented on the manuscript at all stages.
Corresponding author
Ethics declarations
Consent to Participate
This article does not contain any studies with human participants or animals performed by any of the authors.
Conflict of Interest
The authors declare no competing interests.
Additional information
Publisher’s Note
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Supplementary Information
ESM 1
(DOCX 262 kb)
Rights and permissions
About this article
Cite this article
Wang, XD., Chen, K., Cao, DD. et al. The Inhibitory Effect of Cyclodextrin on Oxygen Bioavailability Is a Key Factor for the Metabolic Flux Redistribution Toward Steroid Alcohols in Phytosterol Resting Cells Bioconversion. Appl Biochem Biotechnol 193, 2443–2454 (2021). https://doi.org/10.1007/s12010-021-03540-w
Received:
Accepted:
Published:
Issue Date:
DOI: https://doi.org/10.1007/s12010-021-03540-w


