No abstract

Fourteen isolates of two different bacterial species isolated from the surface of smear-ripened cheeses were found to exhibit many characteristics of the genus Arthrobacter. The isolates were aerobic, Gram-positive, catalase-positive, non-spore-forming and non-motile. The cell-wall peptidoglycan contained lysine, alanine and glutamic acid. rrs sequence analysis indicated that the new isolates Re117T and Ca106T are closely related to the Arthrobacter nicotianae group and showed highest sequence similarity (>98 %) to Arthrobacter nicotianae and Arthrobacter protophormiae. However, DNA–DNA hybridization studies indicated that the strains represented two novel genomic species within the genus Arthrobacter and did not belong to A. nicotianae or A. protophormiae (<43 % DNA–DNA relatedness). On the basis of the phylogenetic and phenotypic distinctiveness of the new isolates, these bacteria should be classified as two novel Arthrobacter species, for which the names Arthrobacter bergerei sp. nov. and Arthrobacter arilaitensis sp. nov. are proposed. Type strains have been deposited in culture collections as Arthrobacter bergerei Ca106T (=CIP 108036T=DSM 16367T) and Arthrobacter arilaitensis Re117T (=CIP 108037T=DSM 16368T).

The enzymatic degradation of L-methionine and subsequent formation of volatile sulfur compounds (VSCs) is believed to be essential for flavor development in cheese. L-Methionine-␥-lyase (MGL) can convert Lmethionine to methanethiol (MTL), ␣-ketobutyrate, and ammonia. The mgl gene encoding MGL was cloned from the type strain Brevibacterium linens ATCC 9175 known to produce copious amounts of MTL and related VSCs. The disruption of the mgl gene, achieved in strain ATCC 9175, resulted in a 62% decrease in thiolproducing activity and a 97% decrease in total VSC production in the knockout strain. Our work shows that L-methionine degradation via ␥-elimination is a key step in the formation of VSCs in B. linens.Due to their low detection threshold and diversity, volatile sulfur compounds (VSCs) are of prime importance in the overall flavor of cheese and make a significant contribution to the typical aromas of different cheeses (12,14,33). VSCs arise primarily from the degradation of L-methionine to methanethiol (MTL) by the cheese microflora. This thiol is a common precursor for a variety of other sulfur-bearing compounds including the auto-oxidation products (11), dimethyl disulfide (DMDS), dimethyl trisulfide (DMTS), and S-methylthioesters, primarily arising from chemical reaction of MTL with acyl coenzyme A (acyl-CoA) (22). Numerous studies have therefore been done to control and/or diversify VSC synthesis during the ripening process by the use of properly selected microorganisms (4, 6, 15, 43). Many cheese microorganisms are capable of producing VSCs from L-methionine. Some of them, such as brevibacteria, especially Brevibacterium linens (17), are known to be very good VSC producers while others, such as lactic acid bacteria (LAB), can produce only limited amounts of VSCs (14).The most direct route for MTL biosynthesis, is the L-methionine ␥-elimination that directly produces MTL, ␣-ketobutyrate, and ammonia from L-methionine. This L-methionine ␥-elimination activity is quite high in B. linens and corynebacteria (17) and is also suspected in several other cheese surface bacteria, such as Micrococcus luteus, Arthrobacter sp., and Staphylococcus equorum (8). In contrast, such activity is quite low in LAB (14). In B. linens, the methionine ␥-elimination is catalyzed by a L-methionine-␥-lyase (MGL), a pyridoxal phosphate (PLP)-dependent enzyme for which L-methionine is the best substrate (16). In contrast, in LAB the reaction is catalyzed by a cystathionine ␤-lyase (CBL) and a cystathionine ␥-lyase (CGL) which are only slightly active towards L-methionine (1, 10, 18). In LAB, another pathway for L-methionine conversion to VSCs also exists but produces limited amounts of MTL (7,35).Coryneform bacteria are generally found on the surface of smear cheeses and give the typical sulfur notes to cheeses such as Limburger, Tilsiter, Livarot, Epoisses, and Munster. To date, B. linens is the only food-grade bacterium from which MGL has been purified and characterized (16,26,31,38,39), but neither its protein sequence nor its gene...

Aims:  This work aimed at clarifying the physiological responses of Lactobacillus delbrueckii subsp. bulgaricus CFL1 cells after exposure to acidification at the end of fermentation, in relation to their cryotolerance. Methods and Results:  Cells acidified at the end of the fermentation (pH 5·25 for 30 min) had their cryotolerance improved as compared to the reference condition (pH 6·0). By analyzing the cytosolic proteome, it was established that changes occurred in the synthesis of 21 proteins, involved in energy metabolism, nucleotide and protein synthesis and stress response. Acidification also induced a slight decrease in unsaturated to saturated and cyclic to saturated membrane fatty acid ratios. Conclusions:  Lactobacillus bulgaricus CFL1 was able to develop a combined physiological response at both membrane and cytosolic levels. This acid adaptation was referred as a cross‐protection phenomenon as it allowed the cells to become more tolerant to cold stress. Significance and Impact of the Study:  This study increased knowledge concerning the physiological mechanisms that explained the cross‐protection by acid adaptation. It may be useful for improving cryotolerance of lactic acid bacteria, either in cells banks or in an industrial context.

The platform molecule 3-hydroxypropionic acid (3-HP) can be produced using Lactobacillus reuteri through a two-step bioprocess that involves a growth phase followed by a bioconversion phase. The bioproduction is performed by resting cells that convert glycerol into 3-HP and 1,3propanediol in fed-batch mode. This work aimed at studying the effect of the growth conditions of L. reuteri DSM 17938 during the first step, on the glycerol bioconversion into 3-HP during the second step. A Plackett and Burman design was carried out to test, in controlled bioreactors, the effect of 11 growth conditions simultaneously, at fixed bioconversion conditions. The supplementation of the growth medium with vitamin B12 and cysteine displayed a negative effect on the 3-HP bioproduction.

Aims:  To help gain a better understanding of factors influencing the establishment within the oral cavity of Streptococcus salivarius K12, a commensal oral bacterium, we characterized its behaviour in artificial saliva. Methods and Results:  Streptococcus salivarius K12 was grown in artificial saliva complemented with a representative meal, under oral pH and temperature conditions. Exponential growth phase was characterized by a high specific growth rate (2·8 h−1). During maintenance phase, an uncoupling between growth and lactic acid production occurred, which allowed maintaining viability (95%), intracellular pH (6·6) and membrane polarisation (95%), and thus proton motive force. However, in late stationary phase, viability (64%) and vitality were degraded as a result of lower synthesis of energetic and glycogen‐related proteins as compared to a richer medium. Conclusions:  Streptococcus salivarius was able to rapidly grow in complemented artificial saliva. Nevertheless, a degradation of its physiological state was observed in late‐stationary phase. Significance and Impact of the Study:  This work demonstrates, for the first time, that artificial saliva was a convenient medium that permitted Strep. salivarius to grow in oral conditions (physico‐chemical environment, addition of meals) but not to maintain cellular viability and vitality in starvation conditions.

-The aromatic potential of various cocultures of yeasts, Brevibacterium linens and lactic acid bacteria (LAB) was studied in cheese-based medium. Three yeasts (Debaryomyces hansenii, Geotrichum candidum and Kluyveromyces lactis) were cultivated in association with B. linens, in the presence or in the absence of LAB -added as the commercial lactic acid starter Flora Danica ® . Various parameters were analysed such as aroma compound production, the growth of each microorganism and lactose/lactate degradation. All tested yeasts could grow in all the associations regardless of the presence or the absence of LAB. LAB enhanced the growth of B. linens in D. hansenii associations, but they reduced B. linens' growth when associated with K. lactis. When cultivated alone, LAB produced very few aroma compounds and in lesser amount than the yeast-B. linens associations. In pure cultures of LAB, ethanol was the major volatile compound, and only scanty amounts of other volatile compounds were produced. The K. lactis-B. linens association exhibited the most diversified aroma compound profile with high quantities of S-methyl thioacetate and ethyl acetate. LAB promoted the synthesis of volatile sulphur compounds in this association.

The relationship between lactose starvation and cryotolerance was investigated in Lactobacillus acidophilus RD758. Cryotolerance was measured from the acidification activity of cells recovered after 18-h lactose starvation. It was compared to that of nonstarved cells, both of them in a stationary phase and in the same medium. This measurement allowed quantifying the initial acidification activity before freezing, as well as the loss of acidification activity during freezing and the rate of loss during frozen storage. Even if initial acidification activity was similar for nonstarved and starved bacteria, the latter displayed a significantly better resistance to freezing and frozen storage at -20°C. To investigate the mechanisms that triggered these cryotolerance phenomena, the membrane fatty acid composition was determined by gas chromatography, and the proteome was established by 2-D electrophoresis, for starved and nonstarved cells. The main outcome was that the improved cryotolerance of starved cells was ascribed to two types of physiological responses as a result of starvation. The first one corresponded to an increased synthesis of unsaturated, cyclic, and branched fatty acids, to the detriment of saturated fatty acids, thus corresponding to enhanced membrane fluidity. The second response concerned the upregulation of proteins involved in carbohydrate and energy metabolisms and in pH homeostasis, allowing the cells to be better prepared for counteracting the stress they encountered during subsequent cold stress. These two phenomena led to a cross-protection phenomenon, which allowed better cryotolerance of Lb. acidophilus RD758, following cellular adaptation by starvation.