Solid-state fermentation of brown seaweeds for the production of alginate lyase using marine bacterium Enterobacter tabaci RAU2C.

IF 4.6 Q2 MATERIALS SCIENCE, BIOMATERIALS
ACS Applied Bio Materials Pub Date : 2024-10-01 Epub Date: 2024-02-24 DOI:10.1007/s12223-024-01150-7
Ramya Petchimuthu, Subharaga Venkatesh, Suriyalakshmi Kannan, Vanavil Balakrishnan
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Abstract

Alginate lyases have countless potential for application in industries and medicine particularly as an appealing biocatalyst for the production of biofuels and bioactive oligosaccharides. Solid-state fermentation (SSF) allows improved production of enzymes and consumes less energy compared to submerged fermentation. Seaweeds can serve as the most promising biomass for the production of biochemicals. Alginate present in the seaweed can be used by alginate lyase-producing bacteria to support growth and can secrete alginate lyase. In this perspective, the current study was directed on the bioprocessing of brown seaweeds for the production of alginate lyase using marine bacterial isolate. A novel alginate-degrading marine bacterium Enterobacter tabaci RAU2C which was previously isolated in the laboratory was used for the production of alginate lyase using Sargassum swartzii as a low-cost solid substrate. Process parameters such as inoculum incubation period and moisture content were optimized for alginate lyase production. SSF resulted in 33.56 U/mL of alginate lyase under the static condition maintained with 75% moisture after 4 days. Further, the effect of different buffers, pH, and temperature on alginate lyase activity was also analyzed. An increase in alginate lyase activity was observed with an increase in moisture content from 60 to 75%. Maximum enzyme activity was perceived with phosphate buffer at pH 7 and 37 °C. Further, the residual biomass after SSF could be employed as biofertilizer for plant growth promotion based on the preliminary analysis. To our knowledge, this is the first report stating the usage of seaweed biomass as a substrate for the production of alginate lyase using solid-state fermentation.

利用海洋细菌 Enterobacter tabaci RAU2C 对褐色海藻进行固态发酵以生产海藻酸酶。
藻酸盐裂解酶在工业和医药领域的应用潜力巨大,尤其是作为生产生物燃料和生物活性低聚糖的生物催化剂具有吸引力。与浸没式发酵相比,固态发酵(SSF)可以提高酶的产量,并消耗更少的能量。海藻是最有希望生产生物化学品的生物质。海藻中的藻酸盐可被产生藻酸盐裂解酶的细菌用来支持生长,并能分泌藻酸盐裂解酶。有鉴于此,本研究旨在利用海洋细菌分离物对褐色海藻进行生物处理,以生产藻酸盐裂解酶。本研究利用之前在实验室中分离到的一种新型海藻酸盐降解海洋细菌 Enterobacter tabaci RAU2C,以马尾藻为低成本固体底物生产海藻酸盐裂解酶。对接种物培养期和含水量等工艺参数进行了优化,以促进藻酸盐裂解酶的生产。在水分含量为 75% 的静态条件下,4 天后 SSF 产生了 33.56 U/mL的藻酸盐裂解酶。此外,还分析了不同缓冲液、pH 值和温度对海藻酸酶活性的影响。随着含水量从 60% 增加到 75%,藻酸盐裂解酶的活性有所增加。在 pH 值为 7、温度为 37 ℃ 的磷酸盐缓冲液中,酶活性最高。此外,根据初步分析,SSF 后的剩余生物质可用作促进植物生长的生物肥料。据我们所知,这是第一份利用固态发酵法将海藻生物质作为生产海藻酸酶底物的报告。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
ACS Applied Bio Materials
ACS Applied Bio Materials Chemistry-Chemistry (all)
CiteScore
9.40
自引率
2.10%
发文量
464
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