Instituto Politécnico Nacional, Unidad Profesional Interdisciplinaria de Biotecnología, Av. Acueducto SN, Col. Barrio la Laguna Ticomán, 07340, Mexico City, Mexico.
Mol Biotechnol. 2019 Jun;61(6):461-468. doi: 10.1007/s12033-019-00177-3.
Synthetic biology and genetic engineering in algae offer an unprecedented opportunity to develop species with traits that can help solve the problems associated with food and energy supply in the 21st century. In the green alga Chlamydomonas reinhardtii, foreign genes can be expressed from the chloroplast genome for molecular farming and metabolic engineering to obtain commodities and high-value molecules. To introduce these genes, selectable markers, which rely mostly on the use of antibiotics, are needed. This has risen social concern associated with the potential risk of horizontal gene transfer across life kingdoms, which has led to a quest for antibiotic-free selectable markers. Phosphorus (P) is a scarce nutrient element that most organisms can only assimilate in its most oxidized form as phosphate (Pi); however, some organisms are able to oxidize phosphite (Phi) to Pi prior to incorporation into the central metabolism of P. As an alternative to the use of the two positive selectable makers already available for chloroplast transformation in C. reinhardtii, the aadA and the aphA-6 genes, that require the use of antibiotics, we investigated if a phosphite-based selection method could be used for the direct recovery of chloroplast transformed lines in this alga. Here we show that following bombardment with a vector carrying the ptxD gene from Pseudomonas stutzeri WM88, only cells that integrate and express the gene proliferate and form colonies using Phi as the sole P source. Our results demonstrate that a selectable marker based on the assimilation of Phi can be used for chloroplasts transformation in a biotechnologically relevant organism. The portable selectable marker we have developed is, in more than 18 years, the latest addition to the markers available for selection of chloroplast transformed cells in C. reinhardtii. The ptxD gene will contribute to the repertoire of tools available for synthetic biology and genetic engineering in the chloroplast of C. reinhardtii.
藻类的合成生物学和基因工程为开发具有特质的物种提供了前所未有的机会,这些特质可以帮助解决 21 世纪与食品和能源供应相关的问题。在绿藻衣藻中,外源基因可以从叶绿体基因组中表达,用于分子农业和代谢工程,以获得商品和高价值分子。为了引入这些基因,需要可选择的标记,这些标记主要依赖于抗生素的使用。这引起了人们对潜在的跨生命王国水平基因转移风险的社会关注,这导致了对无抗生素选择标记的探索。磷(P)是一种稀缺的营养元素,大多数生物只能以磷酸盐(Pi)的最氧化形式同化;然而,一些生物能够在将亚磷酸盐(Phi)氧化为 Pi 之前将其纳入 P 的中心代谢中。作为替代已有的两种在衣藻叶绿体转化中可用的正选择标记aadA 和 aphA-6 的方法,这两种方法都需要使用抗生素,我们研究了是否可以使用基于亚磷酸盐的选择方法直接回收该藻类中的叶绿体转化株。在这里,我们表明,在用携带来自假单胞菌 WM88 的 ptxD 基因的载体轰击后,只有整合并表达该基因的细胞才能以 Phi 作为唯一的 P 源增殖并形成菌落。我们的结果表明,基于 Phi 同化的可选择标记可以用于生物技术相关生物的叶绿体转化。我们开发的可选择标记是继 aadA 和 aphA-6 之后,18 年来在衣藻叶绿体转化中可用的选择标记的最新补充。ptxD 基因将为衣藻叶绿体的合成生物学和基因工程工具库增添新的工具。