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Fundamental Food Microbiology, Third Edition - Fuad Fathir

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152 FUNDAMENTAL FOOD MICROBIOLOGY<br />

6. Production of Folic Acid and Riboflavin ..................................164<br />

7. Enhancing Proteolysis by Cell Lysis .........................................164<br />

C. Protein Targeting ..............................................................................164<br />

1. Expression of Interleukin ...........................................................165<br />

2. Drug-Delivery System ...............................................................165<br />

3. Production of Pediocin in Heterologous Hosts .........................165<br />

D. Protein Engineering .........................................................................166<br />

1. Production of Hybrid Prepediocin .............................................166<br />

2. Amino Acid Variants of Pediocin ..............................................166<br />

V. Genome Mapping and Sequencing ..........................................................166<br />

A. Lactic Acid Bacteria ........................................................................167<br />

B. Bacteriophages .................................................................................168<br />

C. The lac and las Genes .....................................................................168<br />

VI. Conclusion ................................................................................................170<br />

References ............................................................................................................170<br />

Questions ..............................................................................................................171<br />

I. INTRODUCTION<br />

Since the 1930s, it has been recognized that many important characteristics (traits<br />

or phenotypes) in dairy starter-culture bacteria are unstable. For example, a<br />

Lactococcus lactis strain, while growing in milk, once able to ferment lactose<br />

and coagulate the milk, was found to no longer ferment lactose and became<br />

useless commercially. Similar losses of other commercially important traits of<br />

starter cultures used in dairy and nondairy fermentations, such as ability to<br />

hydrolyze proteins (necessary for some cheese production), ability to utilize<br />

citrate (for diacetyl production), resistance to bacteriophages, and hydrolysis of<br />

sucrose, were observed. However, the specific mechanisms involved in the instability<br />

of these important phenotypes were not understood. In the 1960s, the<br />

genetic basis of instability of different microbial phenotypes started unfolding.<br />

Similar studies, when extended to dairy starter-culture bacteria, revealed the<br />

genetic basis of the instability of the important traits. In those days, only a few<br />

laboratories were conducting research in the genetics of lactic acid bacteria<br />

(notably, Dr. Larry McKay's laboratory at the University of Minnesota). Since<br />

the late 1970s, many other laboratories started working in this area and, at present,<br />

genetic research of starter-culture bacteria has generated a major interest in many<br />

laboratories worldwide. The genetic basis of some of the commercially important<br />

phenotypes in some lactic acid bacteria; methods of transfer of desirable traits<br />

from one bacterial strain to another to develop a better strain for use in food<br />

fermentation; and current advances in genetic studies, such as metabolic engineering<br />

and genome sequencing in lactic acid bacteria, are discussed briefly in<br />

this chapter.

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