Microalgal Biotechnology Laboratory, The French Associates Institute for Agriculture and Biotechnology of Drylands, Jacob Blaustein Institute for Desert Research, Ben-Gurion University of the Negev, Sede-Boqer Campus, Midreshet Ben-Gurion 8499000, Israel.
Plant Cell Physiol. 2021 Nov 17;62(9):1478-1493. doi: 10.1093/pcp/pcab094.
A barrier to realizing Nannochloropsis oceanica's potential for omega-3 eicosapentaenoic acid (EPA) production is the disparity between conditions that are optimal for growth and those that are optimal for EPA biomass content. A case in point is temperature: higher content of polyunsaturated fatty acid, and especially EPA, is observed in low-temperature (LT) environments, where growth rates are often inhibited. We hypothesized that mutant strains of N. oceanica resistant to the singlet-oxygen photosensitizer Rose Bengal (RB) would withstand the oxidative stress conditions that prevail in the combined stressful environment of high light (HL; 250 μmol photons m-2 s-1) and LT (18°C). This growth environment caused the wild-type (WT) strain to experience a spike in lipid peroxidation and an inability to proliferate, whereas growth and homeostatic reactive oxygen species levels were observed in the mutant strains. We suggest that the mutant strains' success in this environment can be attributed to their truncated photosystem II antennas and their increased ability to diffuse energy in those antennas as heat (non-photosynthetic quenching). As a result, the mutant strains produced upward of four times more EPA than the WT strain in this HL-LT environment. The major plastidial lipid monogalactosyldiacylglycerol was a likely target for oxidative damage, contributing to the photosynthetic inhibition of the WT strain. A mutation in the NO10G01010.1 gene, causing a subunit of the 2-oxoisovalerate dehydrogenase E1 protein to become non-functional, was determined to be the likely source of tolerance in the RB113 mutant strain.
实现海洋微拟球藻生产 ω-3 二十碳五烯酸 (EPA) 的潜力的一个障碍是,最有利于生长的条件和最有利于 EPA 生物量含量的条件之间存在差异。一个典型的例子是温度:在低温 (LT) 环境中观察到更多的多不饱和脂肪酸,尤其是 EPA,而生长速度往往受到抑制。我们假设,对单线态氧光敏剂孟加拉玫瑰红 (RB) 具有抗性的海洋微拟球藻突变株将能够承受强光 (HL; 250 μmol 光子 m-2 s-1) 和 LT (18°C) 联合胁迫环境中普遍存在的氧化应激条件。这种生长环境导致野生型 (WT) 菌株经历脂质过氧化的激增和无法增殖,而在突变株中观察到生长和内稳态活性氧水平。我们认为,突变株在这种环境中的成功可以归因于它们截短的光系统 II 天线,以及它们在这些天线中以热(非光合猝灭)扩散能量的能力增加。因此,突变株在 HL-LT 环境中产生的 EPA 比 WT 菌株多四倍以上。主要的质体脂质单半乳糖二酰甘油可能是氧化损伤的靶标,导致 WT 菌株的光合作用受到抑制。NO10G01010.1 基因的突变导致 2-氧代异戊酸脱氢酶 E1 蛋白的一个亚基失去功能,被确定是 RB113 突变株耐受的可能来源。