• 제목/요약/키워드: Spore production

검색결과 181건 처리시간 0.023초

표고 톱밥재배용 무포자 신품종 '대담' 육성 및 특성 (Characteristics of newly bred spore-less cultivar Lentinula edodes 'Daedam' for sawdust cultivation)

  • 김정한;강영주;이채영;김연진;최준영;이찬중;하태문;임갑준
    • 한국버섯학회지
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    • 제21권3호
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    • pp.154-159
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    • 2023
  • 표고 톱밥재배용 무포자 품종의 육성을 위해 수집균주 중 우량계통의 단포자 교배를 통해 육성된 '대담'의 주요 특성은 다음과 같다. '대담'의 균사생장 적온은 22~.25℃, 발이 및 생육온도는 16~18℃이었으며, 자실체 형태는 평반구형이며 갓을 형성하지 않는 무포자품종이다. '대담'은 배양기간이 21일, 갈변기간 96일로 대조품종('화담')과 유사하였고, 발이기간은 5일, 생육기간은 9일로 전체 재배기간은 134일로 같았다. '대담'의 개체중은 32.4g으로 대조품종과 유사하였고, 유효개체수는 6.8개로 대조품종 보다 1.3개 낮았으며, 총수량은 222g으로 대조품종의 266g에 비해 낮았다. '대담'의 자실체는 대조품종 대비 갓이 두껍고, 갓 직경은 다소 작았으며, 대의 굵기는 작고 긴 특성을 보였다. '대담'의 배지형태별 생산성 분석결과, 1.2kg 원통형 배지에서 생물학적 효율이 26.7%로 3kg 봉형배지보다 높았으며, '하나참'와 비교 시 재배기간이 40일 짧고 수량도 유사하여, 단기 재배용 품종으로 활용이 가능할 것으로 생각된다.

Fungal bioconversion of Korean food wastes for the production of animal feed additive enzymes

  • 정윤승;정상원;조아라;권순우;한승호
    • 한국생물공학회:학술대회논문집
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    • 한국생물공학회 2001년도 추계학술발표대회
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    • pp.529-532
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    • 2001
  • Korean food waste, one of the abundantly available but environmentally problematic organic wastes in Korea, was utilized as solid-substrate by fungal strain Aspergillus niger ATcC 6275 for the production of enzymemixture containing amylase, cellulase and xylanase. The enzyme mixture can be used as high value-added animal feed. Solid-state fermentation method yielded a 84-fold enhancement in xylanase activity compared with submerged fermentation method. The effect of incubation period, incubation temperature, pH of medium, moisture content, inoculum size and enrichment of the medium with nitrogen and carbon sources were observed for optimal production of these enzymes The optimal amylase activity of 33.10 U/g, cellulase activity of 24.41 U/g, xylanase activity of 328.84 U/g were obtained at 8 days incubation with 50%(w/w) soy bean flake, with incubation temperature of $25^{\circ}C$, pH of 6.38, optimal moisture content of 55% and with inoculum size of $3.8{\times}10^6$spore/g. Enzyme activities were enhanced when ImM $CaSO_4$, 2% Malt extract and 2% galactose were added as mineral, nitrogen and carbon enrichment respectively.

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신규의 Aminopeptidase M 저해제 MR-387A와 B를 생산하는 균주의 동정 및 저해제의 생산 (Taxonobic Characteristics of Strain Producing MR-387A and B,New Inhibitors of Aminopeptidase M,and their Production)

  • 정명철;전효곤;이호재;고영희
    • 한국미생물·생명공학회지
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    • 제22권5호
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    • pp.447-452
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    • 1994
  • The strain SL-387 which produces new inhibitors of aminopeptidase M, MR-387A and B, was isolated from a soil sample. The strain has branched substrate mycelia, from which aerial hyphae develop in the form of open spirals. Spore surface is smooth. Melanoid and soluble pigme- nts were observed. The isolate contains LL-diaminopimelic acid in its cell wall hydrolysate, and has no pectinolytic activity. The strain SL-387 is closely related to Streptomyces griseoruber and S. naganishii, but is different from these strains in some cultural and physiological characteristics. This strain was, therefore, designated as Streptomyces sp. SL-387. The effects of several carbon and nitrogen sources on the production of the inhibitor were examined. Among them, glucose, galactose, mannose, and xylose were effective as a carbon source and soybean meal, soytone, fish meal, and gluten meal were effective as a nitrogen source. The maximum peak of the inhibitor production in jar fermentor was obtained on the fifth day of culture.

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Heterologous Expression of Streptomyces albus Genes Linked to an Integrating Element and Activation of Antibiotic Production

  • Kwon, Hyung-Jin;Lee, Soon-Youl;Hong, Soon-Kwang;Park, Uhn-Mee;Suh, Joo-Won
    • Journal of Microbiology and Biotechnology
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    • 제9권4호
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    • pp.488-497
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    • 1999
  • Probing Streptomyces albus ATCC 21838 chromosomal DNA with a proline tRNA sequence resulted in an isolation of a putative integrating element in the 6.4-kb EcoRI fragment. It was found that Streptomyces lividans TK-24 transformed with a cloned DNA fragment on a multicopy plasmid, produced a higher level of spore pigment and mycelial red pigment on a regeneration agar. Furthermore, the transformant S. lividans TK-24 produced a markedly increased level of undecylprodigiosin in a broth culture. A nucleotide sequence analysis of the cloned region revealed several open reading frames homologous to the integrases of integrating plasmids or temperate bacteriophages, signal-transducing regulatory proteins with a conserved ATP-binding domain, oxidoreductases ($\beta$-ketoacyl reductase), and an AraC-like transcriptional regulator. To examine the effect on antibiotic production, each coding region was overexpressed separately from the other genes in the region in S. lividans TK-24 with; pJHS3044 for the expression of the signal-transducing regulatory protein homologue, pJHS3045 for the homologue of oxidoreductase, and pJHS3051 for the homologue of the AraC-like transcriptional regulator. Phenotypic studies of S. lividans TK-24 strains harboring plasmids for the overexpression of individual genes suggested the following effects of the genes on antibiotic production: The oxidoreductase homologue stimulated the production of actinorhodin and undecylprodigiosin, which was influenced by the culture conditions; the homologue of the AraC-like transcriptional regulator was the most effective factor in antibiotic production within all the culture conditions tested; the signal-transducing regulatory protein homologue repressed the effect due to the homologue of the AraC-like transcriptional regulator, however, the antibiotic production was derepressed upon entering the stationary phase.

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Three Non-Aspartate Amino Acid Mutations in the ComA Response Regulator Receiver Motif Severely Decrease Surfactin Production, Competence Development, and Spore Formation in Bacillus subtilis

  • Wang, Xiaoyu;Luo, Chuping;Liu, Youzhou;Nie, Yafeng;Liu, Yongfeng;Zhang, Rongsheng;Chen, Zhiyi
    • Journal of Microbiology and Biotechnology
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    • 제20권2호
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    • pp.301-310
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    • 2010
  • Bacillus subtilis strains produce a broad spectrum of bioactive peptides. The lipopeptide surfactin belongs to one well-known class, which includes amphiphilic membrane-active biosurfactants and peptide antibiotics. Both the srfA promoter and the ComP-ComA signal transduction system are an important part of the factor that results in the production of surfactin. Bs-M49, obtained by means of low-energy ion implantation in wild-type Bs-916, produced significantly lower levels of surfactin, and had no obvious effects against R. solani. Occasionally, we found strain Bs-M49 decreased spore formation and the development of competence. Blast comparison of the sequences from Bs-916 and M49 indicate that there is no difference in the srfA operon promoter PsrfA, but there are differences in the coding sequence of the comA gene. These differences result in three missense mutations within the M49 ComA protein. RT-PCR analyses results showed that the expression levels of selected genes involved in competence and sporulation in both the wild-type Bs-916 and mutant M49 strains were significantly different. When we integrated the comA ORF into the chromosome of M49 at the amyE locus, M49 restored hemolytic activity and antifungal activity. Then, HPLC analyses results also showed the comA-complemented strain had a similar ability to produce surf actin with wild-type strain Bs-916. These data suggested that the mutation of three key amino acids in ComA greatly affected the biological activity of Bacillus subtilis. ComA protein 3D structure prediction and motif search prediction indicated that ComA has two obvious motifs common to response regulator proteins, which are the N-terminal response regulator receiver motif and the C-terminal helix-turn-helix motif. The three residues in the ComA N-terminal portion may be involved in phosphorylation activation mechanism. These structural prediction results implicate that three mutated residues in the ComA protein may play an important role in the formation of a salt-bridge to the phosphoryl group keeping active conformation to subsequent regulation of the expression of downstream genes.

바실러스 미생물을 이용한 하수처리에서 포기조의 DO농도 변화에 따른 EPS 물질생성과 슬러지 침강성에 관한 연구 (Sedimentation and EPS Production by the Change of Dissolved Oxygen Concentration for the Aeration Tank to treat Wastewater with Bacillus sp.)

  • 이상호;손한형
    • 한국산학기술학회논문지
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    • 제8권3호
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    • pp.627-631
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    • 2007
  • 슬러지의 침전성에 영향을 미치는 인자는 F/M비, 유입수의 성분과 조성, 처리수온, 포기조의 pH, 슬러지 일령, 사상성세균의 증식 등으로 알려져 있으며, 유기산의 잔류량이 EPS의 분비에 영향을 미쳐 슬러지의 침강성에 영향을 주게 된다. 바실러스를 이용한 공법에서 생물 반응조는 특히 바실러스 종의 우점화를 위한 포자화의 진행을 이루는데 중요한 것으로 알려져 있으나 이에 대한 기작 설명은 아직 미흡한 실정이다. 바실러스를 이용한 B3 공법과 RABC 공법으로 운전 중인 처리장의 생물반응조는 점감포기를 하고 있으며 침전조에서 포자를 형성한 바실러스가 생물반응조로 반송되면 1.6mg/L로 높아진 DO농도와 유기물질 유입으로 바실러스가 발아를 하고 활성도가 높아지며, 0.5mg/L로 낮아진 DO농도로 인하여 포자를 형성하면 EPS 추출물질 중 Protein의 함량이 109.95mgEPS/gSS에서 131.77 mg EPS/gSS로 증가하고 SVI는 85mL/g에서 96mL/g사이로 양호함에 따라 DO농도가 EPS 추출물질 중 Protein의 생성에 영향을 미치며 Protein의 함량이 침전에 영향을 미치는 것으로 판단된다. 또한 Protein/Carbohydrate 비율에 따라 침강성은 영향을 받는 것으로 나타났다. 특히 RABC 공법에서는 Protein/Carbohydrate의 비가 침전에 영향을 미치는 것으로 나타난 반면, B3 공법에서는 Protein/carbohydrate의 비에 영향을 크게 받지 않는 것으로 나타났다.

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알로에 베라가 Aspergillus parasiticus의 생육 및 aflatoxin 생성에 미치는 영향 (Effect of Aloe vera on the Growth and Aflatoxin Production of Aspergillus parasiticus)

  • 김종규;이용욱
    • 한국환경보건학회지
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    • 제21권3호
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    • pp.48-55
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    • 1995
  • This study was performed to investigate the inhibitory effect of Aloe vera on the growth and aflatoxin production of Aspergillus parasiticus. Spore suspension of A. parasiticus ATCC 15517 was inoculated on the yeast-extract sucrose broth containing 0.1%, 0.5%, 1.0% and 10.0% of chloroform extract of Aloe vera and then incubated at 30$\circ$C for 7 days. Mycelial weight was 160.7 mg/5ml in control group and decreased by the addition of the extract with no significance. The mold caused decrease in pH of the media with and without the extract. pH in the group contained 10.0% of the extract showed significantly higher value of 5.10 than that of 4.90 in control group (p<0.05). Fluorescence spots of four aflatoxins were observed under the 365 nm of UV light after extraction of the media and TLC. In the result of separation and determination by HPLC, the aflatoxins were produced in the order of $B_1, G_1, B_2$ and $G_2$ in all groups. Production of aflatoxins $B_1, B_2$ and $G_1$ was reduced by the addition of the extract and decreased as amount of the extract increased. The production of aflatoxins $B_1$ and $B_2$ significantly reduced when the media contained more than 1.0% of the extract, and $G_1$ more than 0.5%, respectively(p<0.05). No reduction and no significant difference among groups were observed in case of aflatoxin $G_2$. With the above result, the extract of Aloe vera reduced the production of aflatoxin by A. parasiticus though it did not inhibit mycelial growth.

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감귤과피를 기질로 한 Aspergillus niger의 구연산 발효 (Citric Acid Fermentation from Mandarin Orange Peel by Aspergillus niger)

  • 강신권;박형환;이재호;이윤수;권익부;성낙계
    • 한국미생물·생명공학회지
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    • 제17권5호
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    • pp.510-518
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    • 1989
  • 농산 폐자원 중에서도 감귤 가공공정에 따라 부생되는 감귤과피를 발효 기질로서의 이용을 목적으로 분리균 Asp. niger를 사용하여 구연산 발효에 미치는 배양조건 및 영향인자를 조사하였다. 그 결과 고 체 배양에서의 최적조건 즉 감귤과피와 물을 동량 혼합하고 여기에 NH$_4$NO$_3$0.2%, MgSO$_4$7$H_2O$ 0.1%, Methanol 2.5%를 첨가하여 PH4.5로 조절한 다음포자 현탁액(1x$10^8$ spore/$m\ell$) 2%를 접종하여 균체증식 초기에 35$^{\circ}C$, 20시간 배양하고 4시간 저온 처리한 다음 구연산 생성기에서 3$0^{\circ}C$로 48시간 배양했을 때 당에 대해 80.4%의 높은 수율의 구연산을 얻었다.

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Solid-State Fermentation for the Production of Meroparamycin by Streptomyces sp. strain MAR01

  • El-Naggar, Moustafa Y.;El-Assar, Samy A.;Abdul-Gawad, Sahar M.
    • Journal of Microbiology and Biotechnology
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    • 제19권5호
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    • pp.468-473
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    • 2009
  • The antibiotic meroparamycin was produced in the free culture system of Streptomyces sp. strain MAR01. Five solid substrates (rice, wheat bran, Quaker, bread, and ground corn) were screened for their ability to support meroparamycin production in solid-state fermentation. In batch culture, wheat bran recorded the highest antibacterial activity with the lowest residual substrate values. The highest residual substrate values were recorded for both ground corn and Quaker. On the other hand, no antibacterial activity was detected for rice as a solid substrate. The use of the original strength of starch-nitrate medium in the solid-state fermentation gave a lower antibacterial activity compared with the free culture system. Doubling the strength of this medium resulted in the increase in the activity to be equivalent to the free culture. The initial pH (7.0) of the culture medium and 2 ml of spore suspension (1 ml contains $5{\times}10^{9}spores/ml$) were the optima for antibiotic production. The water was the best eluent for the extraction of the antibiotic from the solid-state culture. Ten min was enough time to extract the antibiotic using a mixer, whereas, 60 min was required when shaking was applied. Semicontinuous production of meroparamycin using a percolation method demonstrated a more or less constant antibacterial activity over 4 runs ($450-480{\mu}g/ml$). The semicontinuous production of the antibiotic was monitored in a fixed-bed bioreactor and the maximum activity was attained after the fourth run ($510{\mu}g/ml$) and the overall process continued for 85 days.

수소생산균 Enterobacter sp. ES392의 분리 및 배양조건 (Isolation and Culture Conditions of Hydrogen Producing Bacterium Enterobacter sp. ES392)

  • 전숭종;이언석
    • 한국미생물·생명공학회지
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    • 제38권4호
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    • pp.399-404
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    • 2010
  • 수소 생산 균주 ES392sms 부산 소재 동의대학교에 위치한 연못 담수에서 분리하였다. 세포는 직경 $0.6\;{\mu}m$, 길이 $1.4\;{\mu}m$의 간균이고 편모와 포자를 형성하지 않았다. 분리된 균주의 16s rRNA 염기서열과 생화학적 특성을 바탕으로 계통학적으로 분류한 결과, ES392 균주는 Enterobacter sp.에 속하는 것으로 동정되었다. 수소생산을 위한 생육최적 pH와 온도는 각각 7.5와 $35^{\circ}C$이었다. 분리한 Enterobacter sp. ES392 균주의 수소생산을 최대화 하기 위해 배지성분을 최적화하였다. 그 결과 4%(w/v) sucrose, 0.5%(w/v) yeast extract, 50 mM potassium phosphate를 첨가한 배지 조건에서 최대수소생산량을 나타내었다. 회분식 배양 조건에서 최대 수소 생산량은 3481 mL/L이었고, 수소생산수율은 1.33mol/mol sucrose를 나타내었다.