• 한국식품영양학회지
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• 제27권1호
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• pp.59-65
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• 2014

들기름 및 미강유를 베이스로 개발한 혼합 식용유는 오메가-3 지방산인 리놀렌산 함량이 약 20% 정도로 매우 높다. 이는 기존의 일반 식용유 중 오메가-3 지방 함량이 매우 높은 콩기름과 카놀라유의 리놀렌산 함량이 각각 6% 및 10% 내외인 점을 감안하면, 이들 식용유에 비하여 새로 들기름과 미강유를 혼합한 식용유는 2~3배 높은 비율로 오메가-3 지방산을 제공할 수 있어서, 오메가-3 지방산 섭취가 부족한 현대인의 식단에서 중요한 오메가-3 지방산 급원으로서의 역할을 할 수 있을 것이다. 뿐만 아니라, 토코페롤 함량도 약 46.77 mg/100 g oil 정도인데, 가장 주목할 일은 토코페롤 동족류 중 비타민 E의 활성이 가장 강한 알파-토코페롤(31.71 mg/100 g oil)이 가장 많이 존재하여, 총 토코페롤의 64%를 차지하고 있어서 비타민 E로서의 기능이 높다. 혈중 콜레스테롤 함량을 낮추는 기능성이 알려진 파이토스테롤 함량이 들기름과 미강유를 혼합한 식용유에 약 7,200 ppm 함유되어 있어, 일반적인 식용유의 3,000 ppm의 약 2.3배에 달한다. 본 연구에서 개발한 들기름과 미강유를 혼합한 식용유는 일반적인 식용유인 콩기름과 거의 유사한 산화안정성을 갖는 것으로 확인되어, 일반 들기름에 비하여 현저히 높은 산화안정성이 확보되었다.

• 한국식품조리과학회지
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• 제4권2호
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• pp.21-30
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• 1988

경북북부지역의 전통음청유인 안동식혜를 Schme 1의 방법으로 제조하여 $12^{\circ}C$에서 48, 60, 72시간동안 발효숙성을 하고 40, 50, $60^{\circ}C$에서는 각각 2, 3, 4시간 발효시킨 후 $12^{\circ}C$에서 20시간 숙성하여 각 조건에서 생성된 비휘발성 유기산과 유리당을 측정하고 관능검사를 한 결과 다음과 같다. 1. 발효온도 $40^{\circ}C$에서 pH는 4.66으로 가장 낮았고 각 온도마다 시간경과에 따라 pH가 떨어지는 경향이었으나 $50^{\circ}C$와 $60^{\circ}C$에서는 2시간을 제외한 3,4시간에서는 시간경과에 따라 pH가 더 높았다. 당도는 12$^{\circ}C$에서 40, 50, $60^{\circ}C$로 온도상승과 2시간에서 3, 4시간 경과에 비례하여 높았다. 2. 총산도는 발효온도가 낮아짐에 따라 반비례적으로 높게 생성되었으며, Oxalate는 control에서만 검출되었을뿐 발효 식혜에서는 거의 생성되지 않았고, Maleate는 $50^{\circ}C$와 $60^{\circ}C$에서, Fumalate는 $60^{\circ}C$에서 생성되지 않았으며 전시료중 가장 많이 생성된 산은 Malate였다. 12$^{\circ}C$에서 48시간은 Malate와 Citrate, Fumalate가 실험조건중 가장 많이 생성되었고, Lactate와 Suc-cinate,그리고 Maleate는 $40^{\circ}C$의 3시간 발효에서 가장많이 생성되었다. 3. 유리당중 Fructose는 control에서 검출된 량과 각 온도별에서 검출된 량이 별 변화를 볼 수 없었으나 그 외 당은 온도상승에 따라 glucose는 2~3배정도, Maltose는 2배 이상 증가하였다. 4. 관능검사결과 $40^{\circ}C$에서 3시간 발효시켜 12$^{\circ}C$에서 20시간 숙성시킨 것이 Fructose 0.45%, Glucose 1.25% 그리고 Maltose 11.5%로서 당도는 14.6%였다 또한 유기산으로는 Lactate Succinate 그리고 Maleate가 실험시료중 제일 많이 생성되어 가장 맛이 있는 것으로 판단되었다.

• Journal of Nutrition and Health
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• 제45권5호
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• pp.429-436
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• 2012

본 연구는 폐기되는 홍게껍질의 단백질을 활용하기 위하여 홍게껍질 분말에 상업적으로 사용하는 6가지 protease를 단일 또는 혼합처리하여 획득한 가용성 가수분해물의 분자량 및 아미노산 조성 등을 비교 분석하여 기능성 소재 및 보충제로서의 활용 가능성을 확인하고자 하였다. 단일효소 6종 중 단백질 분해능은 Biuret assay과 280 nm assay 및 $^{\circ}Brix$로 분석한 결과 Protease A (PA)가 현저하게 높았다. 단일효소 처리로 생성된 가수분해물의 단백질 분자량은 150 kDa 이하의 밴드를 형성하였다. 단일효소 중 단백질 분해능이 가장 강력한 PA의 최적 가수분해 조건을 선정하여 PA에 Protamex (P), Flavourzyme (F), Alcalase (A), Protease M (PM)과 Protease A (PA)를 1대 1의 비로 혼합 (PA + P, PA + PM, PA + F, PA + A)하여 GC로 아미노산 조성을 확인하였다. 총 아미노산 함량은 PA + P 247.411 mg/g > PA + F (206.442 mg/g) > PA + A (133.385 mg/g) > PA + PM (59.131 mg/g) > PA (54.875 mg/g)의 순으로 혼합효소처리가 단일효소처리에 비해 높은 것을 확인할 수 있었다. 혼합효소처리 한 홍게껍질의 아미노산 조성은 사용 효소에 따라 다소 차이가 있었다. 주로 phenylalanine, glycine, alanine, leucine의 함량이 높았으며 tyrosine, cystine은 검출되지 않았다. 쌀을 주식으로 하는 우리나라 사람들에게 부족되기 쉬운 필수 아미노산인 lysine, phenylalnine, leucine, isoleucine의 함량이 높아 아미노산 보충효과를 기대할 수 있을 것으로 보인다.

• 한국구조물진단유지관리공학회 논문집
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• 제23권4호
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• pp.152-158
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• 2019

주차장 바닥재로 많이 사용되는 A사 에폭시 코팅제와 B사 바닥코팅제(A, B type)에 대하여 GC/MS(Gaschromatography/Mass spectrometer)를 이용하여 제품별로 함유하고 있는 휘발성유기화합물(VOCs)의 종류와 함량을 측정해보고, 휘발성유기화합물(VOCs)중 작업자나 입주자들에게 유해한 폼알데하이드(Formaldehyde), 톨루엔(Toluene), 크실렌(Xylene)을 외부 환경에 따른 오차를 줄이고자 가장 안 좋은(밀폐) 환경을 가정하고 가스검지관을 이용하여 가스배출량을 측정해 보았다. 그 결과 A사 에폭시코팅제가 제품 자체에도 휘발성유기화합물(VOCs)을 가장 많은 양 함유하고 있고, A사 에폭시코팅제에 비하여 B사 바닥코팅제 A type은 약 79%, B type은 약 96% 이상의 적은 양을 나타냈다. 또한, 밀폐된 환경 조건에서 1시간과 8시간 경과 후 가스검지관을 이용하여 폼알데하이드(Formaldehyde), 톨루엔(Toluene), 크실렌(Xylene)에 대한 가스배출량을 측정하고 TWA값으로 환산한 결과에서도 A사 에폭시코팅제가 가장 높게 측정되었다. A사 에폭시코팅제보다 B사 바닥코팅제 A type은 약 42.3%이상의 적은 측정값을 나타냈으며, B type의 경우 밀폐된 환경 조건에서도 시간가중평균노출기준(TWA)을 모두 만족하였다.

• Nutrition Research and Practice
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• 제15권3호
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• pp.367-381
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• 2021

BACKGROUND/OBJECTIVES: This study aimed to establish a mother and child cohort in the Chinese population, and investigate human breastmilk (HBM) composition and its relationship with maternal body mass index (BMI) and infant growth during the first 3 mon of life. SUBJECTS/METHODS: A total of 101 Chinese mother and infant pairs were included in this prospective cohort. Alterations in the milk macronutrients of Chinese mothers at 1 mon (T1), 2 mon (T2), and 3 mon (T3) lactation were analyzed. HBM fatty acid (FA) profiles were measured by gas chromatography (GC), and HBM proteomic profiling was achieved by matrix-assisted laser desorption/ionization time-of-flight (MALDI-TOF) mass spectrometry (MS). RESULTS: During the first 3 mon of lactation (P < 0.05), significant decreases were determined in the levels of total energy, fat, protein, and osteopontin (OPN), as well as ratios of long-chain saturated FA (including C16:0, C22:0 and C24:0), monounsaturated FA (including C16:1), and n-6 poly unsaturated FA (PUFA) (including C20:3n-6 and C20:4n-6, and n-6/n-3). Conversely, butyrate, C6:0 and n-3 PUFA C18:3n-3 (α-linolenic acid, ALA) were significantly increased during the first 3 mon (P < 0.05). HBM proteomic analyses distinguished compositional protein differences over time (P = 0.001). Personalized motherinfant analyses demonstrated that HBM from high BMI mothers presented increased total energy, fat, protein and OPN, and increased content of n-6 PUFA (including C18:3n-6, C20:3n-6 and n-6/n-3 ratio) as compared with low BMI mothers (P < 0.05). Furthermore, BMI of the mothers positively correlated with the head circumference (HC) of infants as well as the specific n-6 PUFA C20:3n-6 over the 3 time points examined. Infant HC was negatively associated with C18:0. CONCLUSION: This study provides additional evidence to the Chinese HBM database, and further knowledge of FA function. It also helps to establish future maternal strategies that support the healthy growth and development of Chinese infants.

• Mycobiology
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• 제50권1호
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• pp.66-78
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• 2022

The identification of oleaginous yeast species capable of simultaneously utilizing xylose and glucose as substrates to generate value-added biological products is an area of key economic interest. We have previously demonstrated that the Cutaneotrichosporon dermatis NICC30027 yeast strain is capable of simultaneously assimilating both xylose and glucose, resulting in considerable lipid accumulation. However, as no high-quality genome sequencing data or associated annotations for this strain are available at present, it remains challenging to study the metabolic mechanisms underlying this phenotype. Herein, we report a 39,305,439 bp draft genome assembly for C. dermatis NICC30027 comprised of 37 scaffolds, with 60.15% GC content. Within this genome, we identified 524 tRNAs, 142 sRNAs, 53 miRNAs, 28 snRNAs, and eight rRNA clusters. Moreover, repeat sequences totaling 1,032,129 bp in length were identified (2.63% of the genome), as were 14,238 unigenes that were 1,789.35 bp in length on average (64.82% of the genome). The NCBI non-redundant protein sequences (NR) database was employed to successfully annotate 11,795 of these unigenes, while 3,621 and 11,902 were annotated with the Swiss-Prot and TrEMBL databases, respectively. Unigenes were additionally subjected to pathway enrichment analyses using the Gene Ontology (GO), Kyoto Encyclopedia of Genes and Genomes (KEGG), Cluster of Orthologous Groups of proteins (COG), Clusters of orthologous groups for eukaryotic complete genomes (KOG), and Non-supervised Orthologous Groups (eggNOG) databases. Together, these results provide a foundation for future studies aimed at clarifying the mechanistic basis for the ability of C. dermatis NICC30027 to simultaneously utilize glucose and xylose to synthesize lipids.

• The Plant Pathology Journal
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• 제38권5호
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• pp.541-549
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• 2022

Potato late blight caused by Phytophthora infestans is a destructive disease in Korea. To elucidate the genomic variation of the mitochondrial (mt) genome, we assembled its complete mt genome and compared its sequence among different haplotypes. The mt genome sequences of four Korean P. infestans isolates were revealed by Illumina HiSeq. The size of the circular mt genome of the four major genotypes, KR_1_A1, KR_2_A2, SIB-1, and US-11, was 39,872, 39,836, 39,872, and 39,840 bp, respectively. All genotypes contained the same 61 genes in the same order, comprising two RNA-encoding genes, 16 ribosomal genes, 25 transfer RNA, 17 genes encoding electron transport and ATP synthesis, 11 open reading frames of unknown function, and one protein import-related gene, tatC. The coding region comprised 91% of the genome, and GC content was 22.3%. The haplotypes were further analyzed based on sequence polymorphism at two hypervariable regions (HVRi), carrying a 2 kb insertion/deletion sequence, and HVRii, carrying 36 bp variable number tandem repeats (VNTRs). All four genotypes carried the 2 kb insertion/deletion sequence in HVRi, whereas HVRii had two VNTRs in KR_1_A1 and SIB-1 but three VNTRs in US-11 and KR_2_A2. Minimal spanning network and phylogenetic analysis based on 5,814 bp of mtDNA sequences from five loci, KR_1_A1 and SIB-1 were classified as IIa-6 haplotype, and isolates KR_1_A2 and US-11 as haplotypes IIa-5 and IIb-2, respectively. mtDNA sequences of KR_1_A1 and SIB-1 shared 100% sequence identity, and both were 99.9% similar to those of KR_2_A2 and US-11.

• The Plant Pathology Journal
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• 제38권1호
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• pp.12-24
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• 2022

In this study, we conducted whole-genome sequencing with six species of Pectobacterium composed of seven strains, JR1.1, BP201601.1, JK2.1, HNP201719, MYP201603, PZ1, and HC, for the analysis of pathogenic factors associated with the genome of Pectobacterium. The genome sizes ranged from 4,724,337 bp to 5,208,618 bp, with the GC content ranging from 50.4% to 52.3%. The average nucleotide identity was 98% among the two Pectobacterium species and ranged from 88% to 96% among the remaining six species. A similar distribution was observed in the carbohydrate-active enzymes (CAZymes) class and extracellular plant cell wall degrading enzymes (PCWDEs). HC showed the highest number of enzymes in CAZymes and the lowest number in the extracellular PCWDEs. Six strains showed four subsets, and HC demonstrated three subsets, except hasDEF, in type I secretion system, while the type II secretion system of the seven strains was conserved. Components of human pathogens, such as Salmonella pathogenicity island 1 type type III secretion system (T3SS) and effectors, were identified in PZ1; T3SSa was not identified in HC. Two putative effectors, including hrpK, were identified in seven strains along with dspEF. We also identified 13 structural genes, six regulator genes, and five accessory genes in the type VI secretion system (T6SS) gene cluster of six Pectobacterium species, along with the loss of T6SS in PZ1. HC had two subsets, and JK2.1 had three subsets of T6SS. With the GxSxG motif, the phospholipase A gene did locate among tssID and duf4123 genes in the T6SSa cluster of all strains. Important domains were identified in the vgrG/paar islands, including duf4123, duf2235, vrr-nuc, and duf3396.

• Mycobiology
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• 제51권1호
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• pp.36-48
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• 2023

Xanthoria elegans is a lichen symbiosis, that inhabits extreme environments and can absorb UV-B. We reported the de novo sequencing and assembly of X. elegans genome. The whole genome was approximately 44.63 Mb, with a GC content of 40.69%. Genome assembly generated 207 scaffolds with an N50 length of 563,100 bp, N90 length of 122,672 bp. The genome comprised 9,581 genes, some encoded enzymes involved in the secondary metabolism such as terpene, polyketides. To further understand the UV-B absorbing and adaptability to extreme environments mechanisms of X. elegans, we searched the secondary metabolites genes and gene-cluster from the genome using genome-mining and bioinformatics analysis. The results revealed that 7 NR-PKSs, 12 HR-PKSs and 2 hybrid PKS-PKSs from X. elegans were isolated, they belong to Type I PKS (T1PKS) according to the domain architecture; phylogenetic analysis and BGCs comparison linked the putative products to two NR-PKSs and three HR-PKSs, the putative products of two NR-PKSs were emodin xanthrone (most likely parietin) and mycophelonic acid, the putative products of three HR-PKSs were soppilines, (+)-asperlin and macrolactone brefeldin A, respectively. 5 PKSs from X. elegans build a correlation between the SMs carbon skeleton and PKS genes based on the domain architecture, phylogenetic and BGC comparison. Although the function of 16 PKSs remains unclear, the findings emphasize that the genes from X. elegans represent an unexploited source of novel polyketide and utilization of lichen gene resources.

• Journal of Microbiology and Biotechnology
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• 제33권2호
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• pp.188-194
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• 2023

Microbacterium elymi KUDC0405^T was isolated from the rhizosphere of Elymus tsukushiensis from the Dokdo Islands. The KUDC0405^T strain was Gram-stain-positive, non-spore forming, non-motile, and facultatively anaerobic bacteria. Strain KUDC0405^T was a rod-shaped bacterium with size dimensions of 0.3-0.4 × 0.7-0.8 ㎛. Based on 16S rRNA gene sequences, KUDC0405^T was most closely related to Microbacterium bovistercoris NEAU-LLE^T (97.8%) and Microbacterium pseudoresistens CC-5209^T (97.6%). The dDDH (digital DNA-DNA hybridization) values between KUDC0405^T and M. bovistercoris NEAU-LLE^T and M. pseudoresistens CC-5209^T were below 17.3% and 17.5%, respectively. The ANI (average nucleotide identity) values among strains KUDC0405^T, M. bovistercoris NEAU-LLE^T, and M. pseudoresistens CC-5209^T were 86.6% and 80.7%, respectively. The AAI (average amino acid identity) values were 64.66% and 64.97%, respectively, between KUDC0405^T and its closest related type strains. The genome contained 3,596 CDCs, three rRNAs, 46 tRNAs, and three non-coding RNAs (ncRNAs). The genomic DNA GC content was 70.4%. The polar lipids included diphosphatydilglycerol, glycolipid, phosphatydilglycerol, and unknown phospholipid, and the major fatty acids were anteiso-C_17:0 and iso-C_16:0. Strain KUDC0405^T contained MK-12 as the major menaquinone. Based on genotypic, phylogenetic, and phenotypic properties, strain KUDC0405^T should be considered a novel species within the genus Microbacterium, for which we propose the name M. elymi sp. nov., and the type strain as KUDC0405^T (=KCTC 49411^T, =CGMCC1.18472^T).