Batyrova Khorcheska, Hallenbeck Patrick C
Département de Microbiologie, Infectiologie et Immunologie, Université de Montréal, CP6128 Succursale Centre-ville, Montréal, Québec, QC H3C 3J7, Canada.
Life Sciences Research Center, Department of Biology, United States Air Force Academy, Colorado Springs, CO 80840, USA.
Int J Mol Sci. 2017 Mar 16;18(3):647. doi: 10.3390/ijms18030647.
Chlamydomonas reinhardtii cy6Nac2.49 is a genetically modified algal strain that activates photosynthesis in a cyclical manner, so that photosynthesis is not active constitutively in the presence of oxygen, but is turned on only in response to a metabolic trigger (anaerobiosis). Here, we further investigated hydrogen production by this strain comparing it with the parental wild-type strain under photoheterotrophic conditions in regular tris-acetate-phosphate (TAP) medium with a 10-h:14-h light/dark regime. Unlike the wild-type, whose level of H₂ production remained low during illumination, H₂ production in the mutant strain increased gradually with each subsequent light period, and by the final light period was significantly higher than the wild-type. The relatively low Photosystem II (PSII) activity of the mutant culture was shown by low fluorescence yield both in the dark (Fv/Fm) and in the light (δF/Fm') periods. Measurement of oxygen evolution confirmed the low photosynthetic activity of the mutant cells, which gradually accumulated O₂ to a lesser extent than the wild-type, thus allowing the mutant strain to maintain hydrogenase activity over a longer time period and to gradually accumulate H₂ during periods of illumination. Therefore, controllable expression of PSII can be used to increase hydrogen production under nutrient replete conditions, thus avoiding many of the limitations associated with nutrient deprivation approaches sometimes used to promote hydrogen production.
莱茵衣藻cy6Nac2.49是一种基因工程改造的藻类菌株,它以周期性方式激活光合作用,使得光合作用在有氧存在时并非持续活跃,而是仅在代谢触发因素(无氧状态)下才开启。在此,我们在含有10小时光照/14小时黑暗周期的常规三羟甲基氨基甲烷 - 醋酸盐 - 磷酸盐(TAP)培养基中,在光异养条件下,将该菌株与亲本野生型菌株进行比较,进一步研究了其产氢情况。与野生型不同,野生型在光照期间的产氢水平一直较低,而突变菌株的产氢量在随后的每个光照周期中逐渐增加,到最后一个光照周期时显著高于野生型。突变体培养物相对较低的光系统II(PSII)活性在黑暗(Fv/Fm)和光照(δF/Fm')期间均表现为低荧光产量。氧气释放量的测量证实了突变体细胞的光合活性较低,其积累氧气的程度逐渐低于野生型,从而使突变菌株能够在更长时间内维持氢化酶活性,并在光照期间逐渐积累氢气。因此,PSII的可控表达可用于在营养充足条件下提高产氢量,并避免了有时用于促进产氢的营养剥夺方法所带来的许多限制。