Earticle

현재 위치 Home

Asian Federation of Biotechnology International Symposium :Co-organized by Asian Federation of Biotechnology : Chairs: Duk Jae OH(Sejong University, Korea), Virendra S. BISARIA(Indian Institute of Technology Delhi, India)

Continuous and Pulse Feedings of Crude Glycerol for Bio-molecule Production: the production of L-phenylalanine by recombinant Escherichai coli

첫 페이지 보기
  • 발행기관
    한국생물공학회 바로가기
  • 간행물
    한국생물공학회 학술대회 바로가기
  • 통권
    2010 추계학술대회 및 국제심포지움 (2010.10)바로가기
  • 페이지
    pp.89-89
  • 저자
    Penjit SRINOPHAKUN, A. Thanapimmetha, M. Saisriyoot, K. Thaneeto, M. Khamduang
  • 언어
    영어(ENG)
  • URL
    https://www.earticle.net/Article/A129152

※ 원문제공기관과의 협약기간이 종료되어 열람이 제한될 수 있습니다.

원문정보

초록

영어
In various fermentation products, cost of the carbon source is a significant contributor to the overall cost of the production. Molasses, a by‐product of the sugar factory, is one of the most common carbon sources. However, glycerol is becoming available and inexpensive as the sequence of the rapid growth of biodiesel industry. Generally, every ton of biodiesel produced, nearly a hundred kilograms of crude glycerol is also produced. In fact, pure glycerol has been used in some fermentation processes and additional cost is added to purify glycerol. Therefore, the application of pure glycerol as a carbon source is limited. Escherichai coli is a common microorganisms frequently used as a host in various industrial applications. Interestingly, E. coli is capable of utilizing a variety of carbon sources that are glucose, xylose and fatty acids including glycerol. L‐phenylalanine is the product from E. coli and it is a raw material of low‐caloric sweetener aspartame production. Due to the increasing demand for soft drinks and low‐caloric food, the commercial value of L‐phenylalanine has increased greatly over the past few years. This work presents the production of L‐phenylalanine from crude glycerol using recombinant E. coli BL21 (DE3). The experiment was divided into two parts. The first part was to optimize the medium formula of E. coli BL21 (DE3) for the biomass and L‐phenylalanine productions using Plackett‐Burman Design (P‐BD) and Central Composite Design (C‐CD). The condition of the first part cultivation was 200 rpm of shaking speed and 7.4 of initial pH at constant cultivation temperature of 37˚C. The results showed that, optimum medium formula for the biomass production were crude glycerol of 46.71 g/l, (NH4)2SO4 of 40.55 g/l, KH2PO4 of 1.742 g/l, K2HPO4 of 1.742 g/l, NaCl of 2.554 g/l, MgCl2 of 0.5800 g/l, CaCl2 of 0.0560 g/l, CoCl2 of 0.0036 g/l, ZnSO4 of 0.0113 g/l, CuSO4 of 0.0064 g/l, Na2MoO4 of 0.0069 g/l and yeast extract of 1.411 g/l. In addition, different medium formula was recommended for the L‐phenylalanine production which were crude glycerol of 25.27 g/l, (NH4)2SO4 of 11.53 g/l, KH2PO4 of 0.585 g/l, K2HPO4 of 0.585 g/l, NaCl of 0.859 g/l, MgCl2 of 0.195 g/l, CaCl2 of 0.0567 g/l, CoCl2 of 0.0036 g/l, ZnSO4 of 0.0115 g/l, CuSO4 of 0.0065 g/l, Na2MoO4 of 0.0069 g/l and yeast extract of 1.4263 g/l. In the second part, the fed‐batch cultivation of E. coli BL21 (DE3) was performed. The optimum medium for the biomass production was applied during 0–16 h of cultivation.
After 16th h, the comparison of two different feedings, continuous and pulse feeding operations was carried out. For both feeding the investigation of single substrate feed of crude glycerol and double substrate feeds of crude glycerol and ammonia solution were prepared. The optimum condition of the second part cultivation was 400 rpm of agitation speed, and 6.0 l/min (during 0–16 h and 56–72 h) and 4.0 l/min (during 16–56 h) of aeration rates. The initial volume was 1.3 l, while cultivation temperature and pH were kept constant at 37°C and 7.4. It is obvious that the pulse feeding of crude glycerol and ammonia solution gave the highest biomass and L‐phenylalanine production of 22.71 and 0.781 g/l.

저자

  • Penjit SRINOPHAKUN [ Bioengineering Laboratory, Chemical Engineering Department, Engineering Faculty, Kasetsart University, Thailand. ]
  • A. Thanapimmetha [ Bioengineering Laboratory, Chemical Engineering Department, Engineering Faculty, Kasetsart University, Thailand. ]
  • M. Saisriyoot [ Bioengineering Laboratory, Chemical Engineering Department, Engineering Faculty, Kasetsart University, Thailand. ]
  • K. Thaneeto [ Bioengineering Laboratory, Chemical Engineering Department, Engineering Faculty, Kasetsart University, Thailand. ]
  • M. Khamduang [ Bioengineering Laboratory, Chemical Engineering Department, Engineering Faculty, Kasetsart University, Thailand. ]

참고문헌

자료제공 : 네이버학술정보

간행물 정보

발행기관

  • 발행기관명
    한국생물공학회 [The Korean Society for Biotechnology and Bioengineering]
  • 설립연도
    1984
  • 분야
    공학>생물공학
  • 소개
    이 법인은 생물 공학의 발전과 보급에 이바지하고, 회원 상호 간의 연구 협력과 친목을 도모함을 목적으로 한다 1. 생물공학 분야의 발전을 위한 연구 협력 2. 생물공학의 실용화를 촉진시키기 위한 산학 협동 3. 학술연구 발표회, 강연회, 연수회 등 학술활동의 개최 4. 국,영문 학술지,소식지,학술회의 Proceedings 및 학술도서의 발간 5. 생물공학 발전을 위한 정책 건의 6. 기타 국제 교류 등 본 학회의 목적 달성을 위한 제반 활동

간행물

  • 간행물명
    한국생물공학회 학술대회
  • 간기
    반년간
  • 수록기간
    1985~2013
  • 십진분류
    KDC 476 DDC 576

이 권호 내 다른 논문 / 한국생물공학회 학술대회 2010 추계학술대회 및 국제심포지움

    피인용수 : 0(자료제공 : 네이버학술정보)

    함께 이용한 논문 이 논문을 다운로드한 분들이 이용한 다른 논문입니다.

      페이지 저장