Isolation and characterization of fungi producing L-asparaginase with reduced L-glutaminase activity from soil samples

被引:1
|
作者
Sisay, Tekeba [1 ]
Mobegi, Victor Atunga [2 ]
Wachira, Sabina [3 ]
Maina, Naomi [1 ,4 ]
机构
[1] Pan African Univ, Dept Mol Biol & Biotechnol, Inst Basic Sci Technol & Innovat PAUSTI, Nairobi, Kenya
[2] Univ Nairobi, Fac Sci & Technol, Dept Biochem, Nairobi, Kenya
[3] Kenya Govt Med Res Ctr, Ctr Tradit Med & Drug Res, Nairobi, Kenya
[4] Jomo Kenyatta Univ Agr & Technol, Coll Hlth Sci, Biochem Dept, Nairobi, Kenya
来源
ELECTRONIC JOURNAL OF BIOTECHNOLOGY | 2024年 / 71卷
关键词
Acute lymphoblastic leukemia; Candida; Fungi; L-asparaginase; Reduced L-glutaminase activity; Soil simples; Trichosporon; PLATE ASSAY; EFFICIENT;
D O I
10.1016/j.ejbt.2024.05.002
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Background: L-asparaginase (L-ASNase) is an essential enzyme used to treat acute lymphoblastic leukemia (ALL) by depleting L-asparagine, a vital nutrient for leukemia cells. However, its clinical use is challenged by adverse effects linked to its bacterial origin and L-glutaminase (L-GLNase) co-activity. This study aims to identify fungi capable of producing L-ASNase with reduced L-GLNase co-activity. Results: Among the fungal iolates, isolate JK12 and ChL11 showed high L-ASNase activity (34.04 +/- 1.83a U/ml and 30.84 +/- 0.53b U/ml, respectively) with reduced L-GLNase co-activity (4.95 +/- 0.28c U/ml and 4.80 +/- 0.02d U/ml, respectively). Sequencing of the internal transcribed spacer (ITS) region of these isolates identified them as Candida palmioleophila isolate JK12 (>= 99% identity with Candida genus) and Trichosporon asahii isolate ChL11 (>= 98% identity with Trichosporon genus). Moreover, these isolates exhibited distinct preferences for carbon (C) and nitrogen (N) sources, as well as culture conditions for L-ASNase production. C. palmioleophila isolate JK12 demonstrated the highest L-ASNase production in fructose and yeast extract (67.6 +/- 0.04a U/ml and 51.4 +/- 0.04a U/ml, respectively), following 96 h of incubation at 25 degrees C (43.8 +/- 1.22a U/ml, 55.8 +/- 0.02a U/ml, respectively), with an agitation speed of 100 rpm (59.9 +/- 0.04a U/ml). On the other hand, T. asahii isolate ChL11 exhibited maximum L-ASNase production in sucrose and L-asparagine (64.2 +/- 0.08a U/ml and 63.6 +/- 0.01a U/ml, respectively), after 120 h of incubation at 35 degrees C. Conclusions: The fungal isolates T. asahii isolate ChL11 and C. palmioleophila isolate JK12 have been identified as promising L-ASNase sources of safer therapeutic prospects in cancer therapy due to the reduced GLNase co-activity. How to cite: Sisay T, Mobegi VA, Wachira S, et al. Isolation and characterization of fungi producing L-asparaginase with reduced L-glutaminase activity from soil samples. Electron J Biotechnol 2024. https://doi.org/10.1016/j.ejbt.2024.05.002. (c) 2024 The Author(s). Published by Elsevier Inc. on behalf of Pontificia Universidad Catlica de Valparaso. This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
引用
收藏
页码:10 / 18
页数:9
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