• Biotechnology and Bioprocess Engineering:BBE
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• 제9권6호
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• pp.506-513
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• 2004

Spirulina produces $\gamma$-linolenic acid (GLA), an important pharmaceutical substance, in a relatively low level compared with fungi and plants, prompting more research to improve its GLA yield. In this study, metabolic flux analysis was applied to determine the cellular metabolic flux distributions in the GLA synthetic pathways of two Spiru/ina strains, wild type BP and a high­GLA producing mutant Z19/2. Simplified pathways involving the GLA synthesis of S. platensis formulated comprise of photosynthesis, gluconeogenesis, the pentose phosphate pathway, the anaplerotic pathway, the tricarboxylic cycle, the GLA synthesis pathway, and the biomass syn­thesis pathway. A stoichiometric model reflecting these pathways contains 17 intermediates and 22 reactions. Three fluxes - the bicarbonate (C-source) uptake rate, the specific growth rate, and the GLA synthesis rate - were measured and the remaining fluxes were calculated using lin­ear optimization. The calculation showed that the flux through the reaction converting acetyl­CoA into malonyl-CoA in the mutant strain was nearly three times higher than that in the wild­type strain. This finding implies that this reaction is rate controlling. This suggestion was sup­ported by experiments, in which the stimulating factors for this reaction $(NADPH\;and\;MgCl_{2})$ were added into the culture medium, resulting in an increased GLA-synthesis rate in the wild type strain.

• International Journal of Industrial Entomology and Biomaterials
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• 제33권1호
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• pp.15-23
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• 2016

One major constraint in the development and implementation of a successful and cost-effective area-wide integrated pest management (AW-IPM) programme with a SIT component for Bactrocera oleae (Diptera: Tephritidae) is the ability to produce a large number of high quality mass-reared individuals. The aim of this study was to develop a more efficient and practical egg collection system in an attempt to improve the mass-rearing of this species. The following basic parameters were examined: egg production per female, egg hatch, pupal recovery, pupal weight, adult emergence and percentage of fliers. Three different strains (Israel wild-type, France wild-type, and Greece laboratory) were tested and each strain was evaluated for six generations. Female flies of the Israel strain produced significantly more eggs per female than the other two strains, but egg hatch was significantly lower. Egg hatch of the France wild type and the Greece laboratory strain was similar. For all other parameters, there was no significant difference between strains; however, there was a significant generational effect for all parameters observed. As a result of this study, a protocol was developed for the mass-rearing of this species that included the use of large adult holding cages that could house up to 96,000 flies per cage. The newly developed method of egg collection using a flat wax panel as one of the sides of an adult holding cage proved to be cost-effective, efficient, making colony growth easier for industrial mass-rearing.

• KSBB Journal
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• 제21권2호
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• pp.90-95
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• 2006

라이코펜 생산성을 향상시키기 위하여 몇 가지 대장균 균주들을 대상으로 생산성 시험을 한 결과 MG1655 균주가 가장 우수하였다. 대장균 MG1655 균주의 염색체 DNA 내에 존재하는 특정 유전자의 기능이 상실되었을 때 라이코펜 생산성이 증가되는 변이체를 선발하기 위해 transposon 돌연변이를 수행하였으며, 5종의 우수 transposon 변이체를 얻었다. 특히, Tn4 변이체는 야생형 MG1655에 비해서 라이코펜 생산량은 6배, 균체 내 함량은 7배로 가장 높았다. Transposon 삽입에 의해 결손된 유전자를 파악하기 위해 inverse PCR을 통해 염기서열을 확인하였으며, 결손된 유전자는 rfaH, treB, B2436으로 규명되었다. 또한 특정 유전자 기능의 상실뿐만 아니라 기능의 강화나 변화 등에 의한 라이코펜 생산성이 증가된 변이체를 선발하기 위해 NTG 돌연변이를 수행하였으며, 4개의 우수한 NTG 변이체를 얻었다. 이들 중에 NTG4 변이체가 가장 높은 라이코펜 생산량을 보였다. 특히, NTG4 변이체는 발현유도물질인 arabinose의 소량(0.013mM) 첨가 시에 라이코펜 농도, 6 mg/L와 균체 내 함량 4 mg/g DCW로 최대의 라이코펜 생산성을 보였고, 이것은 야생형 MG1655에 비해서 각각 18배와 12배 높은 생산성이다.

• 생명과학회지
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• 제34권2호
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• pp.79-85
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• 2024

SlyA는 Salmonella와 같은 장내세균과(Enterobacteriaceae)에 속하는 E. coli에서 용혈소(HlyE)의 발현을 조절하는 전사 조절인자로 알려져 있다. 그러나 Salmonella에는 slyA 유전자가 있지만 hlyE 유전자는 없다. Salmonella에서 SlyA의 역할을 탐구하기 위해 slyA 유전자가 결실된 돌연변이주를 사용하였다. S. Typhimurium CK295 (ΔslyA)는 allelic exchange 방법으로 제작되었다. 야생형 균주와 CK295 균주의 비교시험에서 생육 특성, 운동성, 총 단백질 분석, 분비 단백질 분석 등에서 특별한 차이가 발견되지 않았다. CK295 균주는 야생형에 비해 생물막을 약간 적게 생성하는 패턴을 보였다. 흥미롭게도, 대식세포에서의 생존능력을 비교한 결과, CK295 균주는 야생형에 비해 생존능력이 60% 감소하는 것으로 나타났다. 마우스의 독성을 테스트하기 위해 6주령 BALB/c 마우스에 경구 투여한 후 사망률을 측정하였다. 그 결과, BALB/c에서 CK295 (ΔslyA)의 LD₅₀ 값이 야생형 S. Typhimurium 𝜒3339의 값보다 100배 이상 높게 나타났다. 종합적으로, SlyA는 살모넬라균의 in vivo 생존에 관여하는 독성 인자를 코딩하는 유전자의 발현을 조절하는 것으로 추정된다.

• Journal of Microbiology and Biotechnology
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• 제26권4호
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• pp.700-709
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• 2016

The mitogen-activated protein kinase HOG1 (high-osmolarity glycerol response pathway) plays a crucial role in the response of yeast to hyperosmotic shock. Trichosporonoides oedocephalis produces large amounts of polyols (e.g., erythritol and glycerol) in a culture medium. However, the effects of HOG1 gene knockout and environmental stress on the production of these polyols have not yet been studied. In this study, a To-HOG1 null mutation was constructed in T. oedocephalis using the loxP-Kan-loxP/Cre system as replacement of the targeted genes, and the resultant mutants showed much smaller colonies than the wild-type controls. Interestingly, compared with the wild-type strains, the results of shake-flask culture showed that To-HOG1 null mutation increased erythritol production by 1.44-fold while decreasing glycerol production by 71.23%. In addition, this study investigated the effects of citric acid stress on the T. oedocephalis HOG1 null mutants and the wild-type strain. When the supplementation of citric acid in the fermentation medium was controlled at 0.3% (w/v), the concentration of erythritol produced from the wild-type and To-HOG1 knockout mutant strains improved by 18.21% and 21.65%, respectively.

• 대한수의학회지
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• 제53권2호
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• pp.95-101
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• 2013

The study was carried out to evaluate and compare the immune responses in mice experimentally infected with either wild-type or isogenic mutants of Salmonella enterica serovars Enteritidis (SE), Salmonella Typhimurium (ST) and Gallinarum (SG). The mutant strains were constructed by allelic replacement of some virulence-associated genes in the wild-type strains. Seven-week-old female BALB/c mice were orally or intraperitoneally inoculated by injecting bacterial suspension. To evaluate the immune responses, enzyme-linked immunosorbent assay (ELISA) and enzyme-linked immunospot (ELISPOT) assay were conducted with serum and fecal samples. As a result, the mice group infected orally with the SE mutant strain showed the highest level of specific IgA-secreting splenocytes, compared to the other groups. The peritoneally injected groups showed the greater levels of IgG1 than the orally injected groups, which was in a good agreement with the previous studies. In addition, the mutant infected groups had the similar secretion levels of antibodies with the wild-type infected groups. These results demonstrated that the SE mutant strain elicited humoral immune response as much as wild-type, implying that it can be useful as a delivery vehicle as well as a candidate of a live attenuated vaccine.

• Journal of Microbiology and Biotechnology
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• 제20권12호
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• pp.1702-1710
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• 2010

Korean traditional rice wines yakju and takju are generally brewed with nuruk as the source of the saccharogenic enzymes by natural fermentation. To improve the quality of Korean rice wine, the microorganisms in the nuruk need to be studied. The objective of this research was to improve the quality of Korean wine with the wild-type yeast strains isolated from the fermentation starter, nuruk. Only strain YA-6 showed high activity in 20% ethanol. Precipitation of Y89-5-3 was similar to that of very flocculent yeast (>80%) at 75.95%. Using 18S rRNA sequencing, all 10 strains were identified as Saccharomyces cerevisiae. Volatile compounds present in yakju were analyzed by gas chromatography-mass selective detector. The principal component analysis (PCA) of the volatile compounds grouped long-chain esters on the right side of the first principal component, PC1; these compounds were found in yakju that was made with strains YA-6, Y89-5-3, Y89-5-2, Y90-9, and Y89-1-1. On the other side of PC1 were short-chain esters; these compounds were found in wines that were brewed with strains Y183-2, Y268-3, Y54-3, Y98-4, and Y88-4. Overall, the results indicated that using different wild-type yeast strains in the fermentation process significantly affects the chemical characteristics of the glutinous rice wine.

• 한국버섯학회지
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• 제12권3호
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• pp.181-186
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• 2014

본 연구는 느티만가닥버섯 20품종 버섯, 잿빛만가닥 3품종 버섯, 땅지만가닥 1품종 및 돌연변이 느티만가닥버섯 20종류의 유전적 변이를 RAPD 방법에 의해 분석하고자 수행하였다. 이들은 한국, 중국, 일본, 대만 등에서 유래한 것들이다. 느티만가닥버섯에 감마선을 조사하여 돌연변이체를 만들었다. 본 연구에 이용한 primer들은 40종류였고 이 중 31종류의 primer등이 반응을 나타내었다. RAPD 결과들을 분석한 결과 이 들 품종으로는 7개의 cluster로 나뉘어 졌다. 돌연변이체들은 유전적으로 유의적 차이가 있는 subgroup으로 나눌 수 있었다. 이상의 결과들은 본 실험에 사용한 primer들과 포자의 감마선 조사 등을 버섯의 신품종 개발에 유용한 도구가 될 것으로 생각된다.

• Journal of Microbiology and Biotechnology
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• 제26권8호
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• pp.1452-1456
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• 2016

Overexpression of the genes encoding phosphoeneolpyruvate carboxykinase (pckA) and NAD-dependent malic enzyme (maeA) facilitates higher intracellular ATP and NAD(P)H concentrations, respectively, under aerobic conditions in Escherichia coli. To verify a hypothesis that higher intracellular energy reserves might contribute to H₂ fermentation, wild-type E. coli strains overexpressing pckA and maeA were cultured under anaerobic conditions in a glucose minimal medium. Overexpression of pckA and maeA enabled E. coli to produce 3-times and 4-times greater H₂ (193 and 284 nmol, respectively) than the wild type (66 nmol H₂). The pckA and maeA genes were further overexpressed in a hydrogenase-3-enhanced E. coli strain. The hydrogenase-3-enhanced strain (W3110+fhlA) produced 322 nmol H₂, whereas the ATP-enhanced strain (W3110+fhlA+pckA) produced 50% increased H₂ (443 nmol). Total H₂ in the NAD(P)H-enhanced strain (W3110+fhlA+maeA) was similar to that in the control strain at 319 nmol H₂. Possible explanations for the contribution of the increased cellular energy reserves to the enhanced hydrogen fermentation observed are discussed based on the viewpoint of metabolic engineering strategy.

• Journal of Microbiology and Biotechnology
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• 제28권12호
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• pp.2009-2018
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• 2018

Leuconostoc mesenteroides can be used to produce mannitol by fermentation, but the mannitol productivity is not high. Therefore, in this study we modified the chromosome of Leuconostoc mesenteroides by genetic methods to obtain high-yield strains for mannitol production. In this study, gene knock-out strains and gene knock-in strains were constructed by a two-step homologous recombination method. The mannitol productivity of the pat gene (which encodes phosphate acetyltransferase) deletion strain (${\Delta}pat::amy$), the fk gene (which encodes fructokinase) deletion strain (${\Delta}fk::amy$) and the stpk gene (which encodes serine-threonine protein kinase) deletion strain (${\Delta}stpk::amy$) were all increased compared to the wild type, and the productivity of mannitol for each strain was 84.8%, 83.5% and 84.1%, respectively. The mannitol productivity of the mdh gene (which encodes mannitol dehydrogenase) knock-in strains (${\Delta}pat::mdh$, ${\Delta}fk::mdh$ and ${\Delta}stpk::mdh$) was increased to a higher level than that of the single-gene deletion strains, and the productivity of mannitol for each was 96.5%, 88% and 93.2%, respectively. The multi-mutant strain ${\Delta}dts{\Delta}ldh{\Delta}pat::mdh{\Delta}stpk::mdh{\Delta}fk::mdh$ had mannitol productivity of 97.3%. This work shows that multi-gene knock-out and gene knock-in strains have the greatest impact on mannitol production, with mannitol productivity of 97.3% and an increase of 24.7% over wild type. This study used the methods of gene knock-out and gene knock-in to genetically modify the chromosome of Leuconostoc mesenteroides. It is of great significance that we increased the ability of Leuconostoc mesenteroides to produce mannitol and revealed its broad development prospects.