Fatima Iqra, Wakade Geetanjali, Daniell Henry
Department of Basic & Translational Sciences, School of Dental Medicine, University of Pennsylvania, Philadelphia, PA, USA.
Plant Biotechnol J. 2025 Jul;23(7):2689-2703. doi: 10.1111/pbi.70046. Epub 2025 Apr 18.
Candida albicans is a human pathogen responsible for several diseases. C. albicans cell wall contains chitin, glucan and mannan. Therefore, this study evaluated efficacy of enzyme cocktail containing lettuce-expressed chitinases, glucanases and mannanase against C. albicans in cell culture or cancer patient samples. Site-specific integration of the Man1, CelO, Cbh1, Cbh2 expression cassettes and removal of the selectable marker gene from lettuce transplastome was confirmed using three sets of PCR primers. Homoplasmy in transplastomic lines was confirmed in Southern blots by the absence of untransformed genomes. Unlike tobacco, lettuce transplastomic lines had no mosaic phenotype and yielded more biomass than untransformed plants. Maternal inheritance of transgenes was confirmed by lack of segregation when seedlings were germinated in the selection medium. Mannanase expressed in lettuce chloroplasts is thermostable, exhibiting the highest activity at 70 °C; expression increased up to 70 days of growth and is active in a broad range of pH (5-8). Endoglucanases and exoglucanases expressed in lettuce chloroplasts have a broad range of activities between 30 and 75 °C and pH 4-8. Based on observed biomass and mannanase expression level, up to 8640 million enzyme units could be harvested per acre/year. The enzyme cocktail effectively degraded the fungal cell wall, significantly reducing C. albicans viability in cultures and complete inhibition in oral cancer patient samples. Beyond biomedical applications of antifungal drugs, plant cell-based enzyme market is anticipated to double from $52 to >$100 billion in 2028. Edible leaf-based enzyme production offers a new platform that is different from seed-based current technologies for various biotechnology applications.
白色念珠菌是一种可引发多种疾病的人类病原体。白色念珠菌的细胞壁含有几丁质、葡聚糖和甘露聚糖。因此,本研究评估了含有生菜表达的几丁质酶、葡聚糖酶和甘露聚糖酶的酶混合物对细胞培养物或癌症患者样本中的白色念珠菌的功效。使用三组PCR引物确认了Man1、CelO、Cbh1、Cbh2表达盒的位点特异性整合以及从生菜转质体基因组中去除选择标记基因。通过Southern印迹法证实转质体系中的纯合性,即未检测到未转化的基因组。与烟草不同,生菜转质体系没有镶嵌表型,并且比未转化的植物产生更多的生物量。当幼苗在选择培养基中萌发时,由于没有发生分离,从而证实了转基因的母系遗传。生菜叶绿体中表达的甘露聚糖酶具有热稳定性,在70°C时表现出最高活性;表达在生长70天内增加,并且在广泛的pH范围(5-8)内具有活性。生菜叶绿体中表达的内切葡聚糖酶和外切葡聚糖酶在30至75°C和pH 4-8之间具有广泛的活性。根据观察到的生物量和甘露聚糖酶表达水平,每年每英亩可收获多达86.4亿个酶单位。该酶混合物有效地降解了真菌细胞壁,显著降低了培养物中白色念珠菌的活力,并在口腔癌患者样本中实现了完全抑制。除了抗真菌药物的生物医学应用外,预计到2028年,基于植物细胞的酶市场将从520亿美元翻倍至超过1000亿美元。基于可食用叶片的酶生产提供了一个新平台,该平台不同于目前基于种子的各种生物技术应用技术。