高盐度诱导的 L-脯氨酸过量产生的代谢途径工程改善了缺乏外激素的 Halomonas elongata 对高盐度胁迫的耐受性。

IF 3.9 2区 生物学 Q2 BIOTECHNOLOGY & APPLIED MICROBIOLOGY Applied and Environmental Microbiology Pub Date : 2024-09-18 Epub Date: 2024-08-19 DOI:10.1128/aem.01195-24
Huynh Cong Khanh, Pulla Kaothien-Nakayama, Ziyan Zou, Hideki Nakayama
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引用次数: 0

摘要

嗜卤细菌通过积累氨基酸及其衍生物作为有机渗透溶质,适应在高盐度环境中生存。L-脯氨酸(Pro)就是这样一种渗透溶质,在水产养殖业中也被用作饲料刺激剂。Halomonas elongata OUT30018 是一种中度嗜卤细菌,可积累外氨酸(Ect)作为渗透溶质,但不能积累 Pro 作为渗透溶质。由于 elongata OUT30018 能够利用多种生物质衍生的碳源和氮源进行生长,因此本研究利用它来创造一种过量生产 Pro 的菌株,这种菌株可用作富含 Pro 的可持续饲料添加剂。为此,我们用人工自克隆的 proBm1AC 基因簇取代了 H. elongata OUT30018 的 Ect 生物合成操作子的编码区,该基因簇编码 Pro 生物合成酶:反馈抑制不敏感突变体γ-谷氨酸激酶(γ-GKD118N/D119N)、γ-谷氨酰磷酸还原酶和吡咯啉-5-羧酸还原酶。此外,还从基因组中删除了编码 Pro 分解代谢关键酶的 putA 基因,从而产生了 H. elongata HN6。Ect 缺陷的 H. elongata KA1 无法在含超过 4% NaCl 的最小培养基中生长,而 H. elongata HN6 则通过在细胞中积累 Pro 而不是 Ect 在含 8% NaCl 的培养基中茁壮成长,其浓度达到 353.1 ± 40.5 µmol/g 细胞鲜重,与 H. elongata OUT30018 在应对盐胁迫时积累的 Ect 相当。在其遗传背景下,H. elongata HN6 有潜力发展成为一个富含 Pro 的细胞工厂,将生物质废物循环利用为单细胞饲料添加剂,从而为更可持续的水产养殖业做出贡献。值得注意的是,H. elongata HN6(ΔectABC::mCherry-proBm1AC ΔputA)中积累的 Pro 浓度与 H. elongata OUT30018 在高盐度胁迫下积累的外氨酸浓度相当。我们还发现,在两个γ-谷氨酸激酶突变体(γ-GKD118N/D119N和γ-GKD154A/E155A)中,只有γ-GKD118N/D119N突变体对Pro的反馈抑制不敏感。由于Pro是家禽和水产养殖业的重要饲料添加剂之一,因此工程化的H. elongata HN6的基因组成可将高盐度废弃生物质可持续地循环利用为富含Pro的单细胞生态饲料。
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Metabolic pathway engineering of high-salinity-induced overproduction of L-proline improves high-salinity stress tolerance of an ectoine-deficient Halomonas elongata.

Halophilic bacteria have adapted to survive in high-salinity environments by accumulating amino acids and their derivatives as organic osmolytes. L-Proline (Pro) is one such osmolyte that is also being used as a feed stimulant in the aquaculture industry. Halomonas elongata OUT30018 is a moderately halophilic bacterium that accumulates ectoine (Ect), but not Pro, as an osmolyte. Due to its ability to utilize diverse biomass-derived carbon and nitrogen sources for growth, H. elongata OUT30018 is used in this work to create a strain that overproduces Pro, which could be used as a sustainable Pro-rich feed additive. To achieve this, we replaced the coding region of H. elongata OUT30018's Ect biosynthetic operon with the artificial self-cloned proBm1AC gene cluster that encodes the Pro biosynthetic enzymes: feedback-inhibition insensitive mutant γ-glutamate kinase (γ-GKD118N/D119N), γ-glutamyl phosphate reductase, and pyrroline-5-carboxylate reductase. Additionally, the putA gene, which encodes the key enzyme of Pro catabolism, was deleted from the genome to generate H. elongata HN6. While the Ect-deficient H. elongata KA1 could not grow in minimal media containing more than 4% NaCl, H. elongata HN6 thrived in the medium containing 8% NaCl by accumulating Pro in the cell instead of Ect, reaching a concentration of 353.1 ± 40.5 µmol/g cell fresh weight, comparable to the Ect accumulated in H. elongata OUT30018 in response to salt stress. With its genetic background, H. elongata HN6 has the potential to be developed into a Pro-rich cell factory for upcycling biomass waste into single-cell feed additives, contributing to a more sustainable aquaculture industry.IMPORTANCEWe report here the evidence for de novo biosynthesis of Pro to be used as a major osmolyte in an ectoine-deficient Halomonas elongata. Remarkably, the concentration of Pro accumulated in H. elongata HN6 (∆ectABC::mCherry-proBm1AC ∆putA) is comparable to that of ectoine accumulated in H. elongata OUT30018 in response to high-salinity stress. We also found that among the two γ-glutamate kinase mutants (γ-GKD118N/D119N and γ-GKD154A/E155A) designed to resemble the two known Escherichia coli feedback-inhibition insensitive γ-GKD107N and γ-GKE143A, the γ-GKD118N/D119N mutant is the only one that became insensitive to feedback inhibition by Pro in H. elongata. As Pro is one of the essential feed additives for the poultry and aquaculture industries, the genetic makeup of the engineered H. elongata HN6 would allow for the sustainable upcycling of high-salinity waste biomass into a Pro-rich single-cell eco-feed.

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来源期刊
Applied and Environmental Microbiology
Applied and Environmental Microbiology 生物-生物工程与应用微生物
CiteScore
7.70
自引率
2.30%
发文量
730
审稿时长
1.9 months
期刊介绍: Applied and Environmental Microbiology (AEM) publishes papers that make significant contributions to (a) applied microbiology, including biotechnology, protein engineering, bioremediation, and food microbiology, (b) microbial ecology, including environmental, organismic, and genomic microbiology, and (c) interdisciplinary microbiology, including invertebrate microbiology, plant microbiology, aquatic microbiology, and geomicrobiology.
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