Marine Biological Section, University of Copenhagen, Strandpromenaden 5, 3000 Helsingør, Denmark.
Department of Food Chemistry and Toxicology, Faculty of Chemistry, University of Vienna, Währinger Str. 40, 1090 Vienna, Austria.
Harmful Algae. 2022 Feb;112:102173. doi: 10.1016/j.hal.2022.102173. Epub 2022 Jan 10.
Prymnesium parvum causes harmful algal blooms worldwide that are often associated with massive fish-kills and subsequent economic losses. Most of our knowledge of the toxicity of P. parvum derives from bioassays since methods for the identification and quantification of their toxins have been lacking. Recently, a quantitation method was developed for the causative lytic toxins, the prymnesins. Here, we for the first time present data on the influence of irradiance on cellular content and production of prymnesins under nutrient replete conditions in two P. parvum strains, which both produce B-type prymnesins. Large differences were observed between the two strains with regard to the influence of irradiance on prymnesin cell quota and production rates. At the highest irradiance level (550 µmol photons m s), the cellular prymnesin quota was thirty times higher in strain K-0081 strain than in K-0374. The cellular prymnesin quota and production rates were closely linked to rates of growth and photosynthesis in strain K-0081, while this was not the case for K-0374. Yet, growth rate did explain the differences in prymnesin quota in the two strains. Consequently, the maximum prymnesin production rate (414 attomol cell d) was only about three times higher in strain K-0081 than in K-0374, and revealed an optimum at the same irradiance of 200 µmol photons m s in both strains. At low irradiance levels, the difference in production rates between both strains became smaller, with 41 and 49 attomol cell d for K-0081 and K-0374, respectively. The carbon content of prymnesins made up for ∼3% and <1% of the total cellular carbon content in strains K-0081 and K-0374, respectively. The fraction of extracellular dissolved prymnesins was measured for strain K-0081, where it accounted for 14-30% of total prymnesin concentration in the cultures, irrespective of irradiance. The concentrations of prymnesins released to the water by the K-0081 strain were not significantly influenced by irradiance. Overall, we observed comparable responses in growth and photosynthesis of both tested strains toward changes in irradiance. However, the effects of irradiance on prymnesin quota and production rates were remarkably different between the two strains.
多甲藻属(Prymnesium)引起的有害藻类水华在世界各地广泛存在,常导致鱼类大量死亡,并造成后续的经济损失。我们对多甲藻属的毒性的大部分了解来自生物测定,因为缺乏其毒素的鉴定和定量方法。最近,一种定量方法被开发用于鉴定致溶毒素,即多甲藻素。在这里,我们首次提供了在两种产生 B 型多甲藻素的多甲藻属(Prymnesium)菌株中,在营养充足条件下,光照对细胞含量和多甲藻素产生的影响的数据。这两个菌株在光照对多甲藻素细胞配额和产生率的影响方面存在很大差异。在最高光照水平(550 μmol 光子 m s)下,K-0081 菌株的细胞多甲藻素配额比 K-0374 菌株高三十倍。在 K-0081 菌株中,细胞多甲藻素配额和产生率与生长和光合作用速率密切相关,而 K-0374 菌株则不然。然而,生长速率确实解释了这两个菌株中多甲藻素配额的差异。因此,K-0081 菌株的最大多甲藻素产生率(414 attomol 细胞 d)仅比 K-0374 菌株高约三倍,并且在两个菌株中都在 200 μmol 光子 m s 的相同光照下表现出最佳效果。在低光照水平下,两个菌株之间的产率差异变小,K-0081 和 K-0374 菌株的产率分别为 41 和 49 attomol 细胞 d。多甲藻素的碳含量分别占 K-0081 和 K-0374 菌株总细胞碳含量的 3%和<1%。K-0081 菌株细胞外溶解多甲藻素的分数被测量,无论光照如何,它在培养物中占总多甲藻素浓度的 14-30%。K-0081 菌株释放到水中的多甲藻素浓度不受光照的显著影响。总的来说,我们观察到两个受测试菌株在光照变化下的生长和光合作用都有类似的反应。然而,光照对多甲藻素配额和产生率的影响在两个菌株之间有显著的不同。