1.Production of mucic acid from pectin-derived D-galacturonic acid: a review.
Huanghong TAN ; Jing WANG ; Qing LIU ; Zhaojuan ZHENG ; Jia OUYANG
Chinese Journal of Biotechnology 2022;38(2):666-677
Mucic acid is a hexaric acid that can be biosynthesized by oxidation of D-galacturonic acid, which is the main constituent of pectin. The structure and properties of mucic acid are similar to that of glucaric acid, and can be widely applied in the preparation of important platform compounds, polymers and macromolecular materials. Pectin is a cheap and abundant renewable biomass resource, thus developing a process enabling production of mucic acid from pectin would be of important economic value and environmental significance. This review summarized the structure and hydrolysis of pectin, the catabolism and regulation of D-galacturonic acid in microorganisms, and the strategy for mucic acid production based on engineering of corresponding pathways. The future application of mucic acid are prospected, and future directions for the preparation of mucic acid by biological method are also proposed.
Hexuronic Acids/metabolism*
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Pectins/metabolism*
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Sugar Acids/metabolism*
2.Effect of High Glucose on the Oxidative Stress in Trabecular Meshwork Cells.
Jae Woo KIM ; Chang Beum BAE ; Jeong Hun LEE
Journal of the Korean Ophthalmological Society 2009;50(10):1563-1568
PURPOSE: To investigate the effect of high glucose (HG) on the oxidative stress in cultured human trabecular meshwork cells (HTMC). METHODS: Primarily cultured HTMC were exposed to low glucose (5 mM) and HG (25 mM) for 7 days. Additionally, 1 mM L-arginine, 5 mM DAHP, 10 microgram/ml insulin, 100 micrometer L-ascorbic acid, 10, and 100 micrometer sepiapterin were co-exposed. The cellular survival and nitric oxide (NO) production were assessed by MTT assay and Griess assay, respectively. Superoxide production was measured by modified cytochrome c assay. RESULTS: HG did not affect the survival of cultured HTMC significantly. HG decreased NO production. Co-exposed DAHP decreased but DAHP and insulin increased NO production. In addition, HG increased superoxide production, which was decreased by insulin, L-ascorbic acid, and sepiapterin. CONCLUSIONS: HG decreased NO production accompanied with increased superoxide production in HTMC. Thus HG induces oxidative stress in HTMC and may cause cellular dysfunction and damage of the trabecular meshwork.
Arginine
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Ascorbic Acid
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Cytochromes c
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Glucose
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Humans
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Insulin
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Nitric Oxide
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Oxidative Stress
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Pterins
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Sugar Acids
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Superoxides
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Trabecular Meshwork
3.Fitness analysis between the L-sorbosone dehydrogenase modules and Ketogulonigenium vulgare chassis.
Si CHEN ; Nan JIA ; Mingzhu DING ; Yingjin YUAN
Chinese Journal of Biotechnology 2016;32(9):1224-1232
Ketogulonigenium vulgare is an acid-producing strain in the process of two-step vitamin C fermentation. L-sorbosone dehydrogenase (SNDH) is one of the key enzymes during the biosynthesis of 2-keto-L-gulonic acid (2-KGA), the precursor of vitamin C. However, the catalytic mechanism of SNDH is unclear. According to the whole genome sequencing of K. vulgare, two genes encoding sorbosone dehydrogenases, one derived from the chromosome (named as sndhg) and one from plasmid (named as sndhp), were introduced into an industrial strain K. vulgare. The overexpression of gene sndhg had hardly effect on 2-KGA production, and the overexpression of gene sndhp produced an obvious byproduct in the fermentation broth. Combinational expression of sndhg/sndhp with pqqA (obtaining sndhg-pqqA and sndhp-pqqA modules) in K. vulgare resulted in the similar fermentation phenotype to two previous strains. After serial sub-cultivation of co-cultured Bacillus endophyticus with each engineered K. vulgare for 50 d, the conversion rate of 2-KGA increased by 15.4%, 179%, 0.65% and 125% compared with that of the parental K. vulgare with B. endophyticus. This study shows that adaptive evolution of microbial consortium is an effective strategy to increase the fitness between functional modules and chassis, thus quickly getting better strains for production of 2-KGA.
Aldehyde Oxidoreductases
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genetics
;
metabolism
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Ascorbic Acid
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Bacillus
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Bacterial Proteins
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genetics
;
metabolism
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Coculture Techniques
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Fermentation
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Industrial Microbiology
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Microorganisms, Genetically-Modified
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Rhodobacteraceae
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enzymology
;
genetics
;
Sugar Acids
;
metabolism
4.Suppression of CFTR-mediated Cl- Secretion of Airway Epithelium in Vitamin C-deficient Mice.
Yeryung KIM ; Hyemin KIM ; Hae Young YOO ; Jae Seung KANG ; Sung Joon KIM ; Jin Kyoung KIM ; Hyun Sung CHO
Journal of Korean Medical Science 2011;26(3):317-324
Hyperoxic ventilation induces detrimental effects on the respiratory system, and ambient oxygen may be harmful unless compensated by physiological anti-oxidants, such as vitamin C. Here we investigate the changes in electrolyte transport of airway epithelium in mice exposed to normobaric hyperoxia and in gulonolacton oxidase knock-out (gulo[-/-]) mice without vitamin C (Vit-C) supplementation. Short-circuit current (Isc) of tracheal epithelium was measured using Ussing chamber technique. After confirming amiloride-sensitive Na+ absorption (DeltaIsc,amil), cAMP-dependent Cl- secretion (DeltaIsc,forsk) was induced by forskolin. To evaluate Ca2+-dependent Cl- secretion, ATP was applied to the luminal side (DeltaIsc,ATP). In mice exposed to 98% PO2 for 36 hr, DeltaIsc,forsk decreased, DeltaIsc,amil and DeltaIsc,ATP was not affected. In gulo(-/-) mice, both DeltaIsc,forsk and DeltaIsc,ATP decreased from three weeks after Vit-C deprivation, while both were unchanged with Vit-C supplementation. At the fourth week, tissue resistance and all electrolyte transport activities were decreased. An immunofluorescence study showed that the expression of cystic fibrosis conductance regulator (CFTR) was decreased in gulo(-/-) mice, whereas the expression of KCNQ1 K+ channel was preserved. Taken together, the CFTR-mediated Cl- secretion of airway epithelium is susceptible to oxidative stress, which suggests that supplementation of the antioxidant might be beneficial for the maintenance of airway surface liquid.
Animals
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Ascorbic Acid Deficiency/*metabolism
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Biological Transport/drug effects
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Chlorides/*metabolism
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Cystic Fibrosis Transmembrane Conductance Regulator/antagonists & inhibitors/drug
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Forskolin/pharmacology
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Hyperbaric Oxygenation
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Hyperoxia/*physiopathology
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Ion Transport/drug effects
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Mice
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Mice, Inbred C57BL
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Mice, Inbred ICR
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Mice, Knockout/metabolism
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Mice, Transgenic
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Microscopy, Fluorescence
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Oxidative Stress
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Oxygen/adverse effects/pharmacology
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Potassium Channels/metabolism
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Respiratory Mucosa/drug effects/*metabolism/secretion
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Sodium
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Sugar Acids/metabolism
5.Metabolite Profiling during Fermentation of Makgeolli by the Wild Yeast Strain Saccharomyces cerevisiae Y98-5.
Hye Ryun KIM ; Jae Ho KIM ; Byung Hak AHN ; Dong Hoon BAI
Mycobiology 2014;42(4):353-360
Makgeolli is a traditional Korean alcoholic beverage. The flavor of makgeolli is primarily determined by metabolic products such as free sugars, amino acids, organic acids, and aromatic compounds, which are produced during the fermentation of raw materials by molds and yeasts present in nuruk, a Korean fermentation starter. In this study, makgeolli was brewed using the wild yeast strain Saccharomyces cerevisiae Y98-5, and temporal changes in the metabolites during fermentation were analyzed by ultra-high-performance liquid chromatography-quadrupole-time-of-flight mass spectrometry. The resultant data were analyzed by partial least squares-discriminant analysis (PLS-DA). Various metabolites, including amino acids, organic acids, sugar alcohols, small peptides, and nucleosides, were obviously altered by increasing the fermentation period. Changes in these metabolites allowed us to distinguish among makgeolli samples with different fermentation periods (1, 2, 3, 6, 7, and 8 days) on a PLS-DA score plot. In the makgeolli brewed in this study, the amounts of tyrosine (463.13 microg/mL) and leucine (362.77 microg/mL) were high. Therefore, our results indicate that monitoring the changes in metabolites during makgeolli fermentation might be important for brewing makgeolli with good nutritional quality.
Alcoholic Beverages
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Amino Acids
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Amino Sugars
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Fermentation*
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Fungi
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Leucine
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Mass Spectrometry
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Nucleosides
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Nutritive Value
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Peptides
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Saccharomyces cerevisiae*
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Sugar Acids
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Tyrosine
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Yeasts*
6.Systems Biological Approaches Reveal Non-additive Responses and Multiple Crosstalk Mechanisms between TLR and GPCR Signaling.
Jayalakshmi KRISHNAN ; Sangdun CHOI
Genomics & Informatics 2012;10(3):153-166
A variety of ligands differ in their capacity to bind the receptor, elicit gene expression, and modulate physiological responses. Such receptors include Toll-like receptors (TLRs), which recognize various patterns of pathogens and lead to primary innate immune activation against invaders, and G-protein coupled receptors (GPCRs), whose interaction with their cognate ligands activates heterotrimeric G proteins and regulates specific downstream effectors, including immuno-stimulating molecules. Once TLRs are activated, they lead to the expression of hundreds of genes together and bridge the arm of innate and adaptive immune responses. We characterized the gene expression profile of Toll-like receptor 4 (TLR4) in RAW 264.7 cells when it bound with its ligand, 2-keto-3-deoxyoctonate (KDO), the active part of lipopolysaccharide. In addition, to determine the network communications among the TLR, Janus kinase (JAK)/signal transducer and activator of transcription (STAT), and GPCR, we tested RAW 264.7 cells with KDO, interferon-beta, or cAMP analog 8-Br. The ligands were also administered as a pair of double and triple combinations.
Arm
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Gene Expression
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GTP-Binding Proteins
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Heterotrimeric GTP-Binding Proteins
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Immunity, Innate
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Interferon-beta
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Ligands
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Macrophages
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Phosphotransferases
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Sugar Acids
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Toll-Like Receptor 4
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Toll-Like Receptors
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Transcriptome
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Transducers
7.Enhancing 2-keto-L-gulonic acid production under hyperosmotic stress by adding sucrose.
Kejie CHEN ; Jingwen ZHOU ; Liming LIU ; Jie LIU ; Guocheng DU ; Jian CHEN
Chinese Journal of Biotechnology 2010;26(11):1507-1513
This study aimed to further enhance 2-keto-L-gulonic acid (2-KLG) production efficiency. A strategy for enhancing Ketogulonigenium vulgare growth and 2-KLG production by improving B. megaterium growth with sucrose was developed based on the time course of osmolality during 2-KLG industrial scale fermentation and effects of osmolality on cells growth and 2-KLG production. Results showed that the accumulation of 2-KLG and the feeding of alkaline matter led to an osmolality rise of 832 mOsmol/kg in the culture broth. High osmotic stress (1 250 mOsmol/kg) made the growth ofB. megaterium and K. vulgare decreased 15.4% and 31.7%, respectively, and consequently the titer and productivity of 2-KLG reduced 67.5% and 69.3%, respectively. When supplement sucrose under high osmotic condition (1 250 mOsmol/kg), B. megaterium growth was significantly improved, with the result that 2-KLG production was increased 87%. Furthermore, by applying this sucrose addition strategy further to batch fermentation in 3 L fermentor, the productivity of 2-KLG increased 10.4%, and the duration of fermentation declined 10.8%. The results presented here provide a potential strategy for enhancing the target metabolites produced by mixed strains at environmental stress.
Bacillus megaterium
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genetics
;
growth & development
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metabolism
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Fermentation
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Industrial Microbiology
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Osmosis
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Rhodobacteraceae
;
genetics
;
growth & development
;
metabolism
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Stress, Physiological
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Sucrose
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pharmacology
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Sugar Acids
;
metabolism
8.Enhancement of 2-keto-L-gulonic acid production using three-stage pH control strategy.
Jing ZHANG ; Jingwen ZHOU ; Liming LIU ; Jie LIU ; Kejie CHEN ; Guocheng DU ; Jian CHEN
Chinese Journal of Biotechnology 2010;26(9):1263-1268
The aim of this study was to improve the 2-keto-L-gulonic acid (2-KLG) production efficiency by Ketogulonicigenium vulgare and Bacillus megaterium by using multi-stage pH control strategy. The effect of pH on the cell growths and 2-KLG production showed that the optimum pH for K. vulgare and B. megaterium cell growth were 6.0 and 8.0, respectively, while the optimum pH for 2-KLG production was 7.0. Based on the above results, we developed a three-stage pH control strategy: the pH was kept at 8.0 during the first 8 h, then decreased to 6.0 for the following 12 h, and maintained at 7.0 to the end of fermentation. With this strategy, the titer, productivity of 2-KLG and L-sorbose consumption rate were achieved at 77.3 g/L, 1.38 g/(L x h) and 1.42 g/(L x h), respectively, which were 9.7%, 33.2% and 25.7% higher than the corresponding values of the single pH (pH 7.0) control model.
Bacillus megaterium
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growth & development
;
metabolism
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Culture Media
;
chemistry
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Fermentation
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Hydrogen-Ion Concentration
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Rhodobacteraceae
;
growth & development
;
metabolism
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Sorbose
;
metabolism
;
Sugar Acids
;
metabolism
9.Purification of L-sorbose/L-sorbosne dehydrogenase from Ketogulonigenium vulgare and construction and selection of genomic library.
Li XIE ; Duo ZHANG ; Yan-Feng DOU ; Li-Ping ZHANG ; Bao-Hua ZHAO
Chinese Journal of Biotechnology 2007;23(5):891-895
L-sorbose/L-sorbosone dehydrogenase from Ketogulonigenium vulgare S2 can transform L-sorbose to 2-KLG, which is widely used in production of Vitamin C. In order to obtain the engineering strain producing L-sorbose/L-sorbosone dehydrogenase and simplify the fermentation technology, firstly, this enzyme was purified by the methods of ammonium sulfate precipitation, DEAE Sepharose Fast Flow and Q Sepharose High Performance. Then, the purified L-sorbose/L-sorbosone dehydrogenase was injected to rabbit to obtain antibody. Next, the genomic library of Ketogulonigenium vulgare S2 was constructed by inserting the restriction fragments of chromatosomal DNA digested with Sau3A I into cosmid pKC505 vector digested by Hpa I and Pst I, which were packed with lamda phage package protein and transferred into E. coli DH5alpha in vitro. Finally, the positive strain K719# was selected from more than 12,000 clones via Dot-ELISA. Through the test of SDS-PAGE and thin layer chromatography, the results showed that the engineering strain K719# had the same biological activity as Ketogulonigenium vulgare S2 after adding coenzyme PQQ.
Carbohydrate Dehydrogenases
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genetics
;
isolation & purification
;
metabolism
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Cloning, Molecular
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Escherichia coli
;
genetics
;
metabolism
;
Genomic Library
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Gluconobacter oxydans
;
enzymology
;
genetics
;
growth & development
;
Sorbose
;
metabolism
;
Sugar Acids
;
metabolism
;
Transformation, Bacterial
10.Two Cases of Iatrogenic Calcinosis Cutis Following Extravasation of Calcium Gluconate in Neonates.
Eunjin KIM ; Hyunchul PARK ; Jeongeun KIM ; Jooyeon KO ; Youngsuck RO
Korean Journal of Dermatology 2013;51(2):160-161
No abstract available.
Calcinosis
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Calcium
;
Calcium Gluconate
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Gluconates
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Humans
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Infant, Newborn