Melanin Biosynthesis and Omics: Homogentisate Pathway Dysfunction Drives Pyomelanin Production in Mutant Bacillus thuringiensis var. israelensis MB-24.

IF 1.6 3区 生物学 Q3 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Omics A Journal of Integrative Biology Pub Date : 2025-10-01 Epub Date: 2025-09-24 DOI:10.1177/15578100251380105
Nikhil Bharadwaj, Jyothi Nenavath, Muthukumaravel Subramanian, Shubham S Upadhyay, Thottethodi Subrahmanya Keshava Prasad, Sugeerappa L Hoti
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引用次数: 0

Abstract

Melanin is a complex biopolymer with antioxidative, UV-protective, and antimicrobial properties. Melanin is also of interest for bioengineering applications in healthcare. Its production has been frequently observed in several bacteria and higher organisms under specific culture conditions through genetic engineering and chemical mutagenesis. Interestingly, l-DOPA, a precursor to the neurotransmitter dopamine and an effective anti-Parkinsonian drug, has also been frequently observed, at lower levels, along with melanin in the culture of Bacillus thuringiensis, despite the bacterium lacking l-DOPA-producing tyrosinase sequences in the genome. The present study aims to predict the possible l-DOPA-producing enzyme and characterize the melanin biosynthesis pathway in B. thuringiensis var. israelensis MB-24, a strain derived by NTG mutagenesis of entomopathogenic B. thuringiensis var. israelensis B-17. Using metabolomics, we identified the key metabolites involved in melanin production. We also predicted the probable enzyme involved in l-DOPA production through conserved domain search. Sequencing the homogentisate 1,2-dioxygenase (hmgA) gene of MB-24 showed large deletions, suggesting that melanin synthesis may result from accumulated homogentisate in the HGA (Homogentisic acid) pathway. We expressed 4-hydroxyphenyl pyruvate dioxygenase from B. thuringiensis var. israelensis B-17 and characterized the melanin produced by this enzyme through FT-IR (Fourier-Transform Infrared Spectroscopy). The FT-IR analysis further verified that B. thuringiensis var. israelensis MB24 mostly produced pyomelanin. In conclusion, pyomelanin production in B. thuringiensis var. israelensis MB-24 is driven by the homogentisate pathway due to the inability of the mutant bacterium MB-24 to express functional homogentisate 1,2 dioxygenase. These findings inform future industrial and pharmaceutical applications of melanin biosynthesis.

黑色素生物合成和组学:均质通路功能障碍驱动突变体苏云金芽孢杆菌变种以色列芽孢杆菌MB-24的脓黑素产生。
黑色素是一种复杂的生物聚合物,具有抗氧化、防紫外线和抗菌特性。黑色素在医疗保健领域的生物工程应用也引起了人们的兴趣。在特定的培养条件下,通过基因工程和化学诱变,在几种细菌和高等生物中经常观察到它的产生。有趣的是,左旋多巴是神经递质多巴胺的前体,也是一种有效的抗帕金森病药物,尽管苏云金芽孢杆菌的基因组中缺乏左旋多巴产生酪氨酸酶序列,但在培养物中也经常观察到低水平的左旋多巴和黑色素。本研究旨在通过NTG诱变获得的苏云金芽孢杆菌(B. thuringiensis var. israelensis B-17)菌株MB-24中可能产生l- dopa的酶,并对其黑色素生物合成途径进行研究。利用代谢组学,我们确定了参与黑色素产生的关键代谢物。我们还通过保守结构域搜索预测了可能参与左旋多巴产生的酶。对MB-24均质酸1,2-双加氧酶(hmgA)基因进行测序,发现大量缺失,提示黑色素的合成可能是HGA(均质酸)途径中均质酸积累的结果。本文从苏云金芽孢杆菌(B. thuringiensis var. israelensis) B-17中表达了4-羟基苯基丙酮酸双加氧酶,并利用傅里叶变换红外光谱(FT-IR)对该酶产生的黑色素进行了表征。FT-IR分析进一步证实,苏云金芽孢杆菌以色列变种MB24主要产生pyomelanin。综上所述,由于突变菌株MB-24无法表达功能性均质1,2双加氧酶,因此苏云金芽孢杆菌以色列变种MB-24的脓黑素产生是由均质途径驱动的。这些发现为黑色素生物合成的未来工业和制药应用提供了信息。
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来源期刊
Omics A Journal of Integrative Biology
Omics A Journal of Integrative Biology 生物-生物工程与应用微生物
CiteScore
6.00
自引率
12.10%
发文量
62
审稿时长
3 months
期刊介绍: OMICS: A Journal of Integrative Biology is the only peer-reviewed journal covering all trans-disciplinary OMICs-related areas, including data standards and sharing; applications for personalized medicine and public health practice; and social, legal, and ethics analysis. The Journal integrates global high-throughput and systems approaches to 21st century science from “cell to society” – seen from a post-genomics perspective.
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