以酿酒酵母为宿主生产软骨素

SynBio Pub Date : 2024-04-03 DOI:10.3390/synbio2020008
Márcia R. Couto, Joana L. Rodrigues, Oscar Dias, Lígia R. Rodrigues
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引用次数: 0

摘要

软骨素是一种糖胺聚糖,在营养保健品和药品中得到广泛应用,主要用于治疗骨关节炎。传统上,软骨素是从动物软骨中提取的,但最近,生物技术工艺已成为一种商业替代方法,可避免病毒或朊病毒污染的风险,并提供一种素食来源。通常,这些方法是利用病原菌生产软骨素骨架,然后通过磺基转移酶的作用对其进行酶改性。尽管在细菌中表达活性磺基转移酶存在挑战,但真核微生物的使用仍仅限于使用 Pichia pastoris 的少数几项工作。为了创建一个更安全、更高效的生物技术平台,我们在 S. cerevisiae 中构建了一条生产软骨素的生物合成途径,作为概念验证。细胞内和细胞外软骨素的产量分别高达 125 毫克/升和 200 毫克/升。此外,由于基因组尺度模型是确定代谢工程新目标的宝贵工具,我们还开发了软骨素生产 S. cerevisiae 的化学计量模型,并将其用于优化算法。我们的研究发现了几个新的靶点,如二磷酸尿苷 (UDP) -N- 乙酰葡糖胺焦磷酸化酶 (QRI1)、葡糖胺-6-磷酸乙酰转移酶 (GNA1) 或 N- 乙酰葡糖胺-磷酸突变酶 (PCM1),这些靶点可能会提高软骨素的产量,并指导未来的实验研究,为生物技术生产过程开发更高效的宿主生物。
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Saccharomyces cerevisiae as a Host for Chondroitin Production
Chondroitin is a glycosaminoglycan that has gained widespread use in nutraceuticals and pharmaceuticals, mainly for treating osteoarthritis. Traditionally, it has been extracted from animal cartilage but recently, biotechnological processes have emerged as a commercial alternative to avoid the risk of viral or prion contamination and offer a vegan-friendly source. Typically, these methods involve producing the chondroitin backbone using pathogenic bacteria and then modifying it enzymatically through the action of sulfotransferases. Despite the challenges of expressing active sulfotransferases in bacteria, the use of eukaryotic microorganisms is still limited to a few works using Pichia pastoris. To create a safer and efficient biotechnological platform, we constructed a biosynthetic pathway for chondroitin production in S. cerevisiae as a proof-of-concept. Up to 125 mg/L and 200 mg/L of intracellular and extracellular chondroitin were produced, respectively. Furthermore, as genome-scale models are valuable tools for identifying novel targets for metabolic engineering, a stoichiometric model of chondroitin-producing S. cerevisiae was developed and used in optimization algorithms. Our research yielded several novel targets, such as uridine diphosphate (UDP)-N-acetylglucosamine pyrophosphorylase (QRI1), glucosamine-6-phosphate acetyltransferase (GNA1), or N-acetylglucosamine-phosphate mutase (PCM1) overexpression, that might enhance chondroitin production and guide future experimental research to develop more efficient host organisms for the biotechnological production process.
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