Literature DB >> 28529931

Incorporating Fermentation into Undergraduate Laboratory Courses.

Claire Gober1, Madeleine Joullie2.   

Abstract

Laboratory courses in universities have a responsibility to introduce current research practices and trends in scientific research to adequately prepare students for work in the field. One such research practice gaining popularity in recent years is that of green chemistry. Since the 1960s, increasing concern over the release of toxic chemicals into the environment has led to a push for more environmentally responsible chemistry. A growing faction of chemists has begun to adopt methods to eliminate chemical waste and support green chemistry. Fermentation is an ideal technique to demonstrate environmentally sustainable chemistry in an undergraduate laboratory class. Fermentation of complex natural products, as opposed to traditional organic synthesis, is beneficial as it supports a number of principles of green chemistry; it is conducted at ambient temperature and pressure, uses inexpensive and innocuous materials, makes use of renewable resources, and does not require a fume hood. Skills implemented during fermentation can be easily taught to upper-level Chemistry and Biochemistry undergraduate students, who typically have limited exposure to complex natural products in their coursework. Such a course would be interdisciplinary in nature, incorporating fungal biology and metabolism as well as organic chemistry. Students would learn a variety of skills, including growth media selection and preparation, inoculation of fungal cultures, extraction of natural products, and purification and characterization of metabolites. Experiments of this nature would allow for discussions of several areas of research: green chemistry, natural products and their application to medicine, identification of functional groups in complex molecules by spectroscopy, and introduction to biochemistry and metabolism. Roquefortine C, a prenylated indole alkaloid readily produced by a variety of species of Penicillia, is an excellent candidate for demonstrating fermentation in a laboratory classroom setting, owing to its ease of purification from other metabolites and its unique structural features.

Entities:  

Keywords:  Fermentation; Green chemistry; Laboratory instruction; Natural products; Roquefortine C

Year:  2015        PMID: 28529931      PMCID: PMC5438208     

Source DB:  PubMed          Journal:  Athens J Sci        ISSN: 2241-8466


  11 in total

1.  iTRAQ-based proteomic profiling of the barnacle Balanus amphitrite in response to the antifouling compound meleagrin.

Authors:  Zhuang Han; Jin Sun; Yu Zhang; Fei He; Ying Xu; Kiyotaka Matsumura; Li-Sheng He; Jian-Wen Qiu; Shu-Hua Qi; Pei-Yuan Qian
Journal:  J Proteome Res       Date:  2013-04-24       Impact factor: 4.466

2.  A natural short pathway synthesizes roquefortine C but not meleagrin in three different Penicillium roqueforti strains.

Authors:  K Kosalková; R Domínguez-Santos; M Coton; E Coton; C García-Estrada; P Liras; J F Martín
Journal:  Appl Microbiol Biotechnol       Date:  2015-05-22       Impact factor: 4.813

3.  A single cluster of coregulated genes encodes the biosynthesis of the mycotoxins roquefortine C and meleagrin in Penicillium chrysogenum.

Authors:  Carlos García-Estrada; Ricardo V Ullán; Silvia M Albillos; María Ángeles Fernández-Bodega; Pawel Durek; Hans von Döhren; Juan F Martín
Journal:  Chem Biol       Date:  2011-11-23

4.  Molecular requirements for inhibition of cytochrome p450 activities by roquefortine.

Authors:  C Aninat; Y Hayashi; F André; M Delaforge
Journal:  Chem Res Toxicol       Date:  2001-09       Impact factor: 3.739

5.  Total synthesis of isoroquefortine C.

Authors:  Bruno M Schiavi; David J Richard; Madeleine M Joullié
Journal:  J Org Chem       Date:  2002-02-08       Impact factor: 4.354

Review 6.  Recent advances in the biosynthesis of penicillins, cephalosporins and clavams and its regulation.

Authors:  Gulay Ozcengiz; Arnold L Demain
Journal:  Biotechnol Adv       Date:  2012-12-07       Impact factor: 14.227

7.  Oxaline, a fungal alkaloid, arrests the cell cycle in M phase by inhibition of tubulin polymerization.

Authors:  Yukio Koizumi; Masayoshi Arai; Hiroshi Tomoda; Satoshi Omura
Journal:  Biochim Biophys Acta       Date:  2004-07-23

8.  The total synthesis of roquefortine C and a rationale for the thermodynamic stability of isoroquefortine C over roquefortine C.

Authors:  Ning Shangguan; Warren J Hehre; William S Ohlinger; Mary Pat Beavers; Madeleine M Joullié
Journal:  J Am Chem Soc       Date:  2008-04-16       Impact factor: 15.419

9.  Novel key metabolites reveal further branching of the roquefortine/meleagrin biosynthetic pathway.

Authors:  Marco I Ries; Hazrat Ali; Peter P Lankhorst; Thomas Hankemeier; Roel A L Bovenberg; Arnold J M Driessen; Rob J Vreeken
Journal:  J Biol Chem       Date:  2013-11-13       Impact factor: 5.157

10.  A branched biosynthetic pathway is involved in production of roquefortine and related compounds in Penicillium chrysogenum.

Authors:  Hazrat Ali; Marco I Ries; Jeroen G Nijland; Peter P Lankhorst; Thomas Hankemeier; Roel A L Bovenberg; Rob J Vreeken; Arnold J M Driessen
Journal:  PLoS One       Date:  2013-06-12       Impact factor: 3.240

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  2 in total

1.  Fermentation revival in the classroom: investigating ancient human practices as CUREs for modern diseases.

Authors:  Jennifer K Lyles; Monika Oli
Journal:  FEMS Microbiol Lett       Date:  2020-11-23       Impact factor: 2.742

2.  OxaD: A Versatile Indolic Nitrone Synthase from the Marine-Derived Fungus Penicillium oxalicum F30.

Authors:  Sean A Newmister; Claire M Gober; Stelamar Romminger; Fengan Yu; Ashootosh Tripathi; Lizbeth Lorena L Parra; Robert M Williams; Roberto G S Berlinck; Madeleine M Joullié; David H Sherman
Journal:  J Am Chem Soc       Date:  2016-08-24       Impact factor: 15.419

  2 in total

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