Key Laboratory of Tropical Marine Bio-resources and Ecology, Guangdong Key Laboratory of Marine Materia Medica, RNAM Center for Marine Microbiology, South China Sea Institute of Oceanology, Chinese Academy of Sciences, Guangzhou, China.
Key Laboratory of Exploration and Utilization of Aquatic Genetic Resources, International Research Center for Marine Biosciences, Shanghai Ocean University, Shanghai, China.
Microb Biotechnol. 2017 Nov;10(6):1718-1731. doi: 10.1111/1751-7915.12773. Epub 2017 Aug 22.
Members of the marine bacterial genus Pseudoalteromonas are efficient producers of antifouling agents that exert inhibitory effects on the settlement of invertebrate larvae. The production of pigmented secondary metabolites by Pseudoalteromonas has been suggested to play a role in surface colonization. However, the physiological characteristics of the pigments produced by Pseudoalteromonas remain largely unknown. In this study, we identified and characterized a genetic variant that hyperproduces a dark-brown pigment and was generated during Pseudoalteromonas lipolytica biofilm formation. Through whole-genome resequencing combined with targeted gene deletion and complementation, we found that a point mutation within the hmgA gene, which encodes homogentisate 1,2-dioxygenase, is solely responsible for the overproduction of the dark-brown pigment pyomelanin. In P. lipolytica, inactivation of the hmgA gene led to the formation of extracellular pyomelanin and greatly reduced larval settlement and metamorphosis of the mussel Mytilus coruscus. Additionally, the extracted pyomelanin from the hmgA deletion mutant and the in vitro-synthesized pyomelanin also reduced larval settlement and metamorphosis of M. coruscus, suggesting that extracellular pyomelanin released from marine Pseudoalteromonas biofilm can inhibit the settlement of fouling organisms.
海洋细菌假交替单胞菌属的成员是有效的抗菌剂生产者,它们对无脊椎动物幼虫的附着具有抑制作用。假交替单胞菌产生有色次生代谢产物被认为在表面定殖中发挥作用。然而,假交替单胞菌产生的色素的生理特性在很大程度上仍然未知。在这项研究中,我们鉴定并表征了一个遗传变异体,该变异体能大量产生深棕色色素,并且是在假交替单胞菌脂解生物膜形成过程中产生的。通过全基因组重测序结合靶向基因缺失和互补,我们发现 hmgA 基因内的一个点突变,该基因编码 3-羟犬尿氨酸 1,2-双加氧酶,是导致深棕色色素原黑色素过度产生的唯一原因。在假交替单胞菌脂解中,hmgA 基因的失活导致细胞外原黑色素的形成,并大大减少贻贝贻贝幼虫的附着和变态。此外,从 hmgA 缺失突变体中提取的原黑色素和体外合成的原黑色素也减少了贻贝幼虫的附着和变态,表明从海洋假交替单胞菌生物膜释放的细胞外原黑色素可以抑制污损生物的附着。