海洋细菌胞外多糖可拉酸提取及其对厚壳贻贝稚贝附着的作用

Extraction of colanic acid of marine bacteria and its effects on the settlement of Mytilus coruscus plantigrades

  • 摘要:
    目的 为了探究海洋细菌胞外多糖可拉酸(CA)诱导厚壳贻贝附着的机制,
    方法 本研究以厚壳贻贝稚贝为对象,探究可拉酸产生的最适培养条件,并提取纯化进行单糖组成分析,使用不同浓度可拉酸诱导厚壳贻贝附着,注射厚壳贻贝通过荧光定量探究足丝附着效果。
    结果 本研究采用一株高产可拉酸的海假交替单胞菌(Pseudoalteromonas marina ECSMB14103 Δ01912),对其培养条件进行单因素实验、Box-Benhnken中心组合设计优化实验,确定了该菌产生可拉酸的最佳培养方案:pH 为 6.0,培养温度为 30 ℃,培养时间为 18 h,接种量为 8%。通过水沉醇提法提取细菌胞外产物,并使用离子色谱法分析产物的单糖组成,发现提取产物是由岩藻糖、半乳糖、葡萄糖、葡萄糖醛酸按摩尔比 2∶2∶1∶1聚合成的杂多糖,确定提取产物为可拉酸。将可拉酸包埋于琼脂诱导厚壳贻贝稚贝附着,发现可拉酸最佳诱导浓度为 20 和 50 μg/mL。将纯化的可拉酸注射至贻贝体内,通过荧光定量发现,贻贝足丝黏附蛋白基因 Mcfp-1PMcfp-2、Mcfp-5 表达量显著上调,而 Mcfp-1T 表达量在可拉酸处理后没有显著性变化;贻贝足丝胶原蛋白基因 Mccol2 表达量显著上调,而 Mccol3 显著下调。
    结论 研究表明,可拉酸可能是通过调控足丝黏附蛋白和胶原蛋白的分泌,调节厚壳贻贝二次附着。本研究初步揭示了厚壳贻贝的附着机制,同时为可拉酸诱导稚贝附着应用于厚壳贻贝养殖提供潜在价值。

     

    Abstract: To investigate the mechanism by which the exopolysaccharide colanic acid (CA) from marine bacteria induces the attachment of Mytilus coruscus. Juvenile M. coruscus were used as experimental subjects. The optimal culture conditions for CA production were explored, followed by extraction, purification, and monosaccharide composition analysis of CA. Different concentrations of CA were applied to induce mussel attachment, and quantitative real-time polymerase chain reaction (qRT-PCR) was performed after CA injection to evaluate the byssus attachment efficiency. In this study, a genetically engineered strain of Pseudoalteromonas marina ECSMB14103 Δ01912 with high CA production was used. Through single-factor experiments and Box-Benhnken central composite design optimization of extraction culture conditions, the optimal cultivation scheme for CA production in this strain was determined. The optimal scheme for CA production is a pH of 6.0, cultivation temperature of 30°C, cultivation time of 18 h, and inoculum of 8%. Ion chromatography analysis revealed that the product consisted of a heteropolysaccharide composed of fucosylglucose, mannose, glucose, and glucuronic acid in a molar ratio of 2∶2∶1∶1.CA concentrations of 20 μg/mL and 50 μg/mL embedded on glass slides, resulted in the highest inducing activity of M. coruscus plantigrades. Injection of purified CA into mussels showed significant up-regulation of the expression levels of Mcfp-1P, Mcfp-2 and Mcfp-5 genes, which encode adhesive proteins in byssal threads. No significant changes were observed in the expression levels of the Mcfp-1T gene after treatment with CA. Furthermore, the expression level of the Mccol2 gene significantly increased, while Mccol3 expression significantly decreased. These findings suggest that CA may regulate the settlement of M. coruscus plantigrades through promoting secretion of adhesive proteins from byssal threads, and modulating different types of collagen proteins. This study provides a theoretical basis for exploring the mechanism of inducing the settlement of M. coruscus and has potential value in applying acid-induced settlement to the aquaculture of M. coruscus.

     

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