Improving the efficiency and sustainability of chitin bioconversion through a combination of Streptomyces chitin-active-secretomes and mechanical-milling†

IF 9.3 1区 化学 Q1 CHEMISTRY, MULTIDISCIPLINARY Green Chemistry Pub Date : 2023-08-08 DOI:10.1039/D3GC01084H
Lal Duhsaki, Saumashish Mukherjee and Jogi Madhuprakash
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Abstract

Chitin, particularly α-chitin, is the most abundant and highly recalcitrant form, fortified by an intricate network of hydrogen bonds. Efficient valorization of α-chitin requires mild pre-treatment and enzymatic hydrolysis. Streptomyces spp. secrete chitin-active CAZymes that can efficiently tackle the recalcitrant problem of chitin biomass. To better understand the potential of Streptomyces spp., a comparative analysis was performed between the novel isolate, Streptomyces sp. UH6 and the well-known chitin degraders, S. coelicolor and S. griseus. Growth studies and FE-SEM analysis revealed that all three Streptomyces spp. could utilize and degrade both α- and β-chitin. Zymogram analysis showed expression of 5–7 chitinases in the secretomes of Streptomyces strains. The chitin-active-secretomes produced by Streptomyces sp. UH6 and S. griseus were optimally active at acidic pH (pH 4.0 and 5.0) and 50 °C. Time-course degradation of α- and β-chitin with the secretomes generated N-acetyl-D-glucosamine (GlcNAc) and N,N-diacetylchitobiose [(GlcNAc)2] as the predominant products. Further, the highly crystalline α-chitin was subjected to pre-treatment by ball-milling, which reduced the crystallinity from 88% to 56.6% and increased the BET surface area by 3-folds. Of note, the activity of all three Streptomyces secretomes was improved by a mild pre-treatment, while Streptomyces sp. UH6 secretome displayed improved GlcNAc and (GlcNAc)2 yields by 14.4 and 9.6-folds, respectively. Overall, our results suggest that the Streptomyces chitin-active-secretomes, particularly Streptomyces sp. UH6, can be deployed for efficient valorization of chitin biomass and to establish an economically feasible and eco-friendly process for valorizing highly recalcitrant α-chitin.

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通过链霉菌的几丁质活性分泌体和机械加工的结合提高几丁质生物转化的效率和可持续性
几丁质,尤其是α-几丁质,是最丰富和最顽固的形式,由一个复杂的氢键网络加强。α-几丁质的有效活化需要温和的预处理和酶水解。链霉菌分泌的几丁质活性酶可以有效地解决几丁质生物量的顽固性问题。为了更好地了解Streptomyces spp.的潜力,我们将新分离的Streptomyces sp. UH6与著名的几质降解物S. coelicolor和S. griseus进行了比较分析。生长研究和FE-SEM分析表明,这3种链霉菌都能利用和降解α-和β-几丁质。酶谱分析显示,链霉菌分泌组中有5-7种几丁质酶的表达。Streptomyces sp. UH6和S. griseus产生的几丁质活性分泌体在酸性pH (pH 4.0和5.0)和50°C条件下具有最佳活性。分泌组降解α-和β-几丁质时,主要产物为N-乙酰-d -氨基葡萄糖(GlcNAc)和N,N-二乙酰壳聚糖[(GlcNAc)2]。对高结晶度α-几丁质进行球磨预处理,结晶度由88%降至56.6%,BET表面积增加3倍。值得注意的是,这三种链霉菌分泌组的活性都得到了温和的预处理,而链霉菌UH6分泌组的GlcNAc和(GlcNAc)2的产量分别提高了14.4倍和9.6倍。总之,我们的研究结果表明,链霉菌的几丁质活性分泌体,特别是链霉菌UH6,可以用于几丁质生物量的有效增殖,并建立一个经济上可行和环保的方法来增殖高顽固的α-几丁质。
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来源期刊
Green Chemistry
Green Chemistry 化学-化学综合
CiteScore
16.10
自引率
7.10%
发文量
677
审稿时长
1.4 months
期刊介绍: Green Chemistry is a journal that provides a unique forum for the publication of innovative research on the development of alternative green and sustainable technologies. The scope of Green Chemistry is based on the definition proposed by Anastas and Warner (Green Chemistry: Theory and Practice, P T Anastas and J C Warner, Oxford University Press, Oxford, 1998), which defines green chemistry as the utilisation of a set of principles that reduces or eliminates the use or generation of hazardous substances in the design, manufacture and application of chemical products. Green Chemistry aims to reduce the environmental impact of the chemical enterprise by developing a technology base that is inherently non-toxic to living things and the environment. The journal welcomes submissions on all aspects of research relating to this endeavor and publishes original and significant cutting-edge research that is likely to be of wide general appeal. For a work to be published, it must present a significant advance in green chemistry, including a comparison with existing methods and a demonstration of advantages over those methods.
期刊最新文献
Back cover Measuring green chemistry: methods, models, and metrics Inside back cover Back cover Development of a highly efficient electrocatalytic hydrogenation and dehalogenation system using a flow cell with a Pd tube cathode
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