• Biotechnology and Bioprocess Engineering:BBE
• /
• 제9권4호
• /
• pp.245-251
• /
• 2004

The fungal species of Rhizopus oryzae 2062 has the capacity to carry out a single stage fermentation process for lactic acid production from potato starch wastewater. Starch hydrolysis, reducing sugar accumulation, biomass formation, and lactic acid production were affected with variations in pH, temperature, and starch source and concentration. A growth condition with starch concentration approximately 20 g/ L at pH 6.0 and 30$^{\circ}C$ was favourable for starch fermentation, resulting in a lactic acid yield of 78.3%∼85.5% associated with 1.5∼2.0 g/L fungal biomass produced in 36 h of fermentation.

• Journal of Microbiology and Biotechnology
• /
• 제2권4호
• /
• pp.288-292
• /
• 1992

Kinetics of anaerobic ethanol fermentation by Clostridium thermohydrosulfuricum were investigated for the one-step production of ethanol from starch. A mutant strain with a high ethanol yield was induced from C. thermohydrosulfuricum. The mutant, designated as ME4, produced anaerobically 6.1 g/l of ethanol, 3.1 g/l of lactate and 0.1 g/l of acetate from 20 g/l of starch at $68^{\circ}C.

• 한국미생물·생명공학회지
• /
• 제11권3호
• /
• pp.181-185
• /
• 1983

증자하지 않은 Cassava의 생전분의 ethanol 발효생산을 위하여 Aspergilius shirousami 가생산하는 당화효소를 이용하여 단순당화 및 동시당화 발효를 하였다. Cassava 생전분의 당화률은 증자한 것에 비해 30% 정도였으며 10배의 효소를 가하여도 60%밖에 안되었으나. 동시당화-발효에서는 당화율이 크게 증가하여 ethanol 생성량이 증자한 전분에 비해 90% 이상이 되었다.

• 한국식품영양과학회지
• /
• 제31권3호
• /
• pp.405-410
• /
• 2002

생전분 분해효소를 이용한 타피오카의 당화 및 알콜 병행복발효에 적합한 조건을 조사하였다. 그 결과 가수량 250% (v/w), 효소제 사용량 0.5%(w/w)를 사용하여 96시간 발효하였을 때 알콜 함량이 가장 높았다. 알콜발효 96시간째에 알콜함량 및 환원당은 11.7% 및 306mg%으로 각각 나타났다. pH 변화는 발효초기 pH 6.2에서 발효 후 pH 4.2 범위로 감소하였으며, 총산은 발효초기 0.11에서 0.43가지 증가하였으나 큰 변화는 없었다. 알콜성분은 ethanol, methanol, iso-propanol, n-proylalcohol, iso-butylalcohol 및 iso-amylalcohol이 분석되었으며 그외에 acetaldehyde가 확인되었다. 생전분분해효소제를 이용한 타피오카의 알콜발효 조건은 가수량250%, 효소제 0.5%로 설정할 수 있었다. 그러나 전반적인 발효수율은 증자방법에 비하여 낮게 나타났다.

• 한국미생물·생명공학회지
• /
• 제24권6호
• /
• pp.726-732
• /
• 1996

To improve the fermentation characteristics(such as starch-degradability, ethanol tolerance, sugar and high-temperature tolerance) of recombinant haploid yeast Saccharomyces diastaticus K114, hybridization technique was used. The hybridization partner was S. diastaticus 1177 which had good glucoamylase activity and fermentabi- lity. The best hybrid HH64 showed improved ethanol tolerance, sugar and high-temperature tolerance. Especia- lly, the starch-fermentability was significantly improved, since the hybrid produced 1.60% (w/v) ethanol from 4% (w/v) starch, while the recombinant haploid K114 produced 1.30% (w/v) ethanol. The optimum temperature and pH for the starch-fermentation by the hybrid HH64 was 30$\circ$C and 5, respectively. The hybrid yeast HH64 produced 7.5% (w/v) ethanol directly from 20% (w/v) starch.

• 한국식품과학회지
• /
• 제27권5호
• /
• pp.773-775
• /
• 1995

The effect of alum$(Al{\cdot}K(SO_4)_2{\cdot}12H_{2}O)$ on the activity of raw starch-digesting enzyme produced by alkali-tolerant Bacillus sp. was investigated. In adding alum of 0.5%(w/w), activities of raw starch-digesting enzyme on the gelatinized and raw rice starches have not been inhibited. In case of adding alum of 5%(w/w), competitive and uncompetitive inhibition were observed for the gelatinized and raw rice starches, respectively. The inhibitory effect on the raw starch was much higher than that on the gelatinized starch.

• 한국식품과학회지
• /
• 제53권5호
• /
• pp.514-520
• /
• 2021

본 연구에서는 찹쌀풀 첨가량에 따른 김치를 제조하여 저장기간에 따라 김치의 품질 특성, 당과 관련된 대사산물, 전분 구조 변화를 분석하였다. 찹쌀풀 함량이 높을수록 김치의 발효과정이 가속화하여 pH의 감소와 총균수의 증가 속도가 빠른 경향을 보여 상대적으로 빠르게 김치의 적숙기에 도달하였다. 이러한 결과는 찹쌀풀의 전분을 빠르게 가수분해하여 많은 양의 전분 유래대사산물인 glucose, maltose, mannitol을 생성하였으며, 반대로 fructose와 sorbitol 함량은 낮은 경향을 나타냈다. 김치발효 중 찹쌀풀 함량이 높을수록 아밀로펙틴 긴 사슬은 감소한 반면 짧은 사슬의 비율은 증가하였다. 결과적으로 김치 제조 시 첨가되는 찹쌀풀의 함량에 따라 전분 구조의 차이를 나타냈으며 이에 따른 대사산물과 이화학적 특성에 영향을 미치는 것을 확인하였다.

• Journal of Microbiology and Biotechnology
• /
• 제20권4호
• /
• pp.718-726
• /
• 2010

A selected fungal strain, for production of the raw-starchdigesting enzyme by solid-state fermentation, was improved by two repeated sequential exposures to ${\gamma}$-irradiation of $Co^{60}$, ultraviolet, and four repeated treatments with Nmethyl-N'-nitrosoguanidine. The mutant strain Aspergillus sp. XN15 was chosen after a rigorous screening process, with its production of the raw-starch-digesting enzyme being twice that of usual wild varieties cultured under preoptimized conditions and in an unsupplemented medium. After 17 successive subculturings, the enzyme production of the mutant was stable. Optimal conditions for the production of the enzyme by solid-state fermentation, using wheat bran as the substrate, were accomplished for the mutant Aspergillus sp. XN15. With the optimal fermentation conditions, and a solid medium supplemented with nitrogen sources of 1% urea and 1% $NH_4NO_3$, 2.5 mM $CoSO_4$, 0.05% (v/w) Tween 80, and 1% glucose, the mutant Aspergillus sp. XN15 produced the raw-starch-digesting enzyme in quantities 19.4 times greater than a typical wild variety. Finally, XN15, through simultaneous saccharification and fermentation of a raw rice corn starch slurry, produced a high level of ethanol with $Y_{p/s}$ of 0.47 g/g.

• Journal of Microbiology and Biotechnology
• /
• 제19권10호
• /
• pp.1161-1168
• /
• 2009

Ethanol production by the simultaneous saccharification and fermentation (SSF) of low-value rice wine cake (RWC) without cooking was investigated. RWC is the filtered solid waste of fermented rice wine mash and contains 53% raw starch. For the SSF, the RWC slurry was mixed with the raw-starch-digesting enzyme of Rhizopus sp. and yeast, where the yeast strain was selected from 300 strains and identified as Saccharomyces cerevisiae KV25. The highest efficiency (94%) of ethanol production was achieved when the uncooked RWC slurry contained 23.03% starch. The optimal SSF conditions were determined as 1.125 units of the raw-starch-digesting enzyme per gram of RWC, a fermentation temperature of $30^{\circ}C$, slurry pH of 4.5, 36-h-old seeding culture, initial yeast cell number of $2{\times}10^7$ per ml of slurry, 17 mM of urea as the nitrogen additive, 0.25 mM of $Cu^{2+}$ as the metal ion additive, and a fermentation time of 90 h. Under these optimal conditions, the ethanol production resulting from the SSF of the uncooked RWC slurry was improved to 16.8% (v/v) from 15.1% (v/v) of pre-optimization.

• Asian-Australasian Journal of Animal Sciences
• /
• 제31권10호
• /
• pp.1611-1618
• /
• 2018

Objective: The objective of this experiment was to examine the effects of different amylose/amylopectin ratios on rumen fermentation and development of fattening lambs. Methods: Forty-eight 7-day-old male Small-tailed Han sheep${\times}$Northeast fine wool sheep were randomly assigned to four treatments of dietary amylose/amylopectin ratios (0.12, 0.23, 0.24, and 0.48 in tapioca starch, corn starch, wheat starch and pea starch diets, respectively). Three lambs from each treatment were slaughtered at 21, 35, 56, and 77 days of age to determine the rumen fermentation and development. Results: Compared with tapioca starch diet, the pea starch diet significantly increased the concentration of ammonia nitrogen in the ruminal fluid of lambs but significantly decreased the bacterial protein content. At 56 and 77 d, the rumen propionate concentration tended to be greatest in the tapioca starch group than in other groups. The rumen butyrate concentration was the greatest in lambs fed on pea starch compared with those fed on other starch diets. Furthermore, the pea starch diet significantly stimulated rumen development by increasing the papillae height, width and surface area in the rumen ventral or dorsal locations in lambs. However, different amylose/amylopectin ratios diets did not significantly affect the feed intake, body weight, average daily gain, the relative weight and capacity of the rumen in lambs with increasing length of trial periods. Conclusion: Lambs early supplemented with a high amylose/amylopectin ratio diet had favourable morphological development of rumen epithelium, which was not conducive to bacterial protein synthesis.